31st International Symposium on Chirality - Programme - 14th - 17th July 2019 Bordeaux, France - Chirality 2019
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31st International
Symposium on Chirality
14th - 17th July 2019
Bordeaux, France Chirality
2019
Programme
Programme
WELCOME TO
BORDEAUX
CONTENT It is our great pleasure to welcome you to Bordeaux for the 31st International
Symposium on Chirality - CHIRALITY 2019 held at ENSEIRB MATMECA, located
on the campus of the University of Bordeaux, a short tram ride away from the centre
of Bordeaux―the “Port of the Moon”―and its UNESCO world heritage-protected,
historic centre created in the Age of Enlightenment.
This annual three and a half days event is dedicated to state-of-the-art research
Welcome note page 3 in various fields of chirality, and was first organised in 1991. CHIRALITY 2019 in
International committee page 4 Bordeaux follows the previous meetings held in Princeton (2018), Tokyo (2017),
Local organising committee page 5 Heidelberg (2016), Boston (2015), and Prague (2014).
Invited speakers page 6
Chirality Medal 2019 page 8 During this 2019 conference, achievements in enantioseparation from some of the
Practical information page 10-11 founders of the CHIRALITY conference will be highlighted by invited speakers.
Also, the annual Chirality Medal will be award to a researcher who has made significant
Bordeaux general information page 12-13
contributions to this field over the course of his career. This year, the Chirality Medal
Gala dinner page 14-15 winner is Professor Laurence A. Nafie from Syracuse University, USA.
Partners & sponsors page 16
Programme This exciting programme brings together students, postdoc fellows and established
Sunday 14th July page 17 researchers from academia, as well as industrialists, with topics covering the whole
Monday 15th July page 18 to 21 spectrum of chirality research.
Tuesday 16th July page 22 to 25
Wednesday 17th July page 26 to 28 CHIRALITY 2019 was made possible only through the generous help of our sponsors
Poster sessions page 29 to 37 and we thank them for all their support.
Programme overview page 54
We also wish to thank all the local organisers, students and postdocs, as well as
Venue page 55 the advisory board and the past organisers for their valuable advice.
We hope that you will have a great CHIRALITY 2019 experience
and that you will enjoy the beautiful city of Bordeaux and its surroundings.
Reiko ODA, University of Bordeaux, Chair
Jeanne CRASSOUS, University of Rennes 1, Co-chair
2 3
INTERNATIONAL LOCAL ORGANISING
COMMITTEE COMMITTEE
◆ Toru ASAHI, Waseda University, Japan ◆ Reiko ODA, CBMN, University of Bordeaux / CNRS / Bordeaux INP, Chair
◆ Isao AZUMAYA, Chiba University, Japan ◆ Jeanne CRASSOUS, University of Rennes 1 / CNRS, Co-chair
◆ Zachary S. BREITBACH, AbbVie Inc., North Chicago, USA ◆ Thierry BUFFETEAU, ISM, University of Bordeaux / CNRS
◆ James CANARY, New York University, USA ◆ Nicolas DAUGEY, ISM, University of Bordeaux / CNRS
◆ Albert CHAN, Hong Kong Polytechnic University, China Scientific ◆ Yann FERRAND, CBMN, University of Bordeaux / CNRS / Bordeaux INP
◆ Jeanne CRASSOUS, University of Rennes 1, France & ◆ Gilles GUICHARD, CBMN, University of Bordeaux / CNRS / Bordeaux INP
Executive ◆ Lorenzo DI BARI, University of Pisa, Italy organising ◆ Elizabeth HILLARD, CRPP, University of Bordeaux / CNRS
committee committee ◆ Brice KAUFFMANN, IECB, University of Bordeaux / CNRS
◆ Bart KAHR, New York University, USA
◆ Jérôme LACOUR, University of Geneva, Switzerland ◆ Yannick LANDAIS, ISM, University of Bordeaux / CNRS
◆ Oliver TRAPP, University of Munich, Germany ◆ Sylvain NLATE, CBMN, University of Bordeaux / CNRS / Bordeaux INP
◆ Claudio VILLANI, Sapienza University of Rome, Italy ◆ Emilie POUGET, CBMN, University of Bordeaux / CNRS / Bordeaux INP
◆ David WALBA, University of Colorado, Boulder, USA ◆ Vincent RODRIGUEZ, ISM, University of Bordeaux / CNRS
◆ R. Thomas WILLIAMSON, University of North Carolina, USA ◆ Patrick ROSA, ICMCB, University of Bordeaux / CNRS
◆ Eiji YASHIMA, Nagoya University, Japan
◆ Daniel W. ARMSTRONG, Arlington TX, USA
◆ Nina D. BEROVA, New York, NY, USA
Honorary advisory ◆ John CALDWELL, Liverpool, UK
committee ◆ Eric FRANCOTTE, Basel, Switzerland
◆ Wolfgang LINDNER, Vienna, Austria
◆ Yoshio OKAMOTO, Nagoya, Japan
◆ Kazuhiko SAIGO, Kochi, Japan
◆ Christopher WELCH, Indiana, USA
◆ Domenico MISITI, Rome, Italy - retired 2010
◆ Vadim A. DAVANKOV, Moscow, Russia - retired 2007
◆ Volker SCHURIG, Tübingen, Germany - retired 2006
Emeritus ◆ Irving WAINER, Washington, USA - retired 2000
members ◆ Bernard TESTA, Lausanne, Switzerland - retired 1998
◆ Anthony FELL, Bradford, UK - retired 1999
◆ Uli HACKSELL, Stockholm, Sweden - retired 1995
◆ André COLLET, Lyon, France - Deceased 1999
◆ William PIRKLE, Urbana, USA - retired 2001, deceased 2017
4 5
INVITED
SPEAKERS
Plenary speakers
◆ Donald HILVERT, ETH Zurich, Switzerland
◆ Nicholas KOTOV, University of Michigan, USA
◆ Alexander KUHN, University of Bordeaux / CNRS / Bordeaux INP, France
◆ Laurence A. NAFIE, Syracuse University, USA
◆ Virginie SIMONET, CNRS / Grenoble Alpes University, France
◆ Michinori SUGINOME, Kyoto University, Japan
Keynote speakers
◆ Narcis AVARVARI, University of Angers, France
◆ Petr BOUR, University of Chemistry and Technology, Prague, Czech Republic
◆ Zachary BREITBACH, AbbVie Inc., USA
◆ Chiara CAPPELLI, Scuola Normale Superiore, Italy
◆ Shunai CHE, Shanghai Jiao Tong University, China
◆ Jonathan CLAYDEN, University of Bristol, UK
◆ Lorenzo DI BARI, University of Pisa, Italy
◆ Stephen FLETCHER, University of Oxford, UK
◆ Pilar FRANCO, Chiral Technologies, France
◆ Hirotaka IHARA, University of Kumamoto, Japan
◆ Nathalie KATSONIS, University of Twente, The Netherlands
◆ Jérôme LACOUR, University of Geneva, Switzerland
◆ Giovanna LONGHI, University of Brescia, Italy
◆ Keiji MARUOKA, Kyoto University, Japan
◆ Cornelia MEINERT, University of Côte d’Azur, France
◆ Anja PALMANS, Eindhoven University of Technology, The Netherlands
◆ Jun SHEN, Harbin Engineering University, China
◆ Jay SIEGEL, Tianjin University, China
◆ Oliver TRAPP, Ludwig-Maximilians University, Germany
◆ Joanna WENCEL-DELORD, University of Strasbourg, France
◆ Eiji YASHIMA, Nagoya University, Japan
◆ Jieping ZHU, Ecole Polytechnique Fédérale de Lausanne, Switzerland
6 7
CHIRALITY
MEDAL 2019
The Chirality Medal was instituted by the Societa Chimica Italiana in 1991 to honor internationally recognized
scientists who have made a distinguished contribution to all aspects of chirality. It is awarded each year by a
Chirality Medal Honor Committee comprising the Chirality International Committee members and the most
recent recipients of the medal. This year, we will be honored to award
Professor Laurence (Larry) A. NAFIE
Distinguished Professor Emeritus in Chemistry, Syracuse University (USA),
world-wide recognized specialist of Vibrational Optical Activity
Prof. Larry Nafie receives the honor for his seminal contributions to the development and application of
vibrational optical activity (VOA). VOA comprises two powerful complementary chiroptical spectroscopies:
infrared vibrational circular dichroism (VCD) and vibrational Raman optical activity (ROA), both of which
provide complete three-dimensional solution structures, including absolute configuration, of chiral molecules.
In 1974, while a postdoctoral associate in the laboratory of Philip Stephens (1940-2012) at the University
of Southern California, Larry Nafie confirmed and extended the first reported VCD spectrum published
earlier that year from the laboratory of George Holzwarth at the University of Chicago. Using a superior
VCD instrument design (based on the fabrication of the first ZnSe photoelastic modulator, now used in all
VCD spectrometers), he published with Tim Keiderling and Philip Stephens, the first major paper on VCD.
Thanks to his groundbreaking papers, Larry was appointed to the faculty of Syracuse University in 1975, the
first to be hired in the USA specifically to pursue a career in VCD. Due to his doctoral research experience
at the University of Oregon with Raman spectroscopy, he extended his program to include ROA, thereby
establishing the first laboratory dedicated to research in both VCD and ROA. His ensuing research made vital
contributions to the theory, instrumentation, measurement and application of both VCD and ROA spanning 35
years until his retirement from Syracuse University in 2010.
Especially important was the development in his laboratory in 1979 of a Fourier transform (FT) instrument
for measuring VCD. Commercial FT-VCD instruments based on this design are now used in both academic
and pharmaceutical research laboratories around the world. The advent of a practical VCD instrument has
made a huge impact on many areas of chemistry, biochemistry and medicinal chemistry. Additionally he was
the first to measure ROA using the circular polarization content of Raman spectra which he named scattered
circular polarization (SCP) ROA, now the basis of all commercial ROA instruments. Further, he has made
fundamental contributions to the foundations of the theory of VOA including the vibronic coupling theory of
VCD, nuclear velocity dependence of VCD and vibrational electron current density, resonance ROA, and VCD
in molecules with low-lying electronic states. Among many other things, VOA has become one of the most
important and reliable methods to determine the absolute configuration of single-enantiomer drug molecules.
BioTools, Inc., which was co-founded by Prof. Nafie and Dr. Rina Dukor in 1996 for the commercialization
of VOA, offered the first dedicated spectrometer for the measurement of VCD in 1997 and of ROA in 2003.
The living scientist who had the most to do with this major innovation in chiral analysis is undoubtedly
Prof. Larry Nafie. We address our warmest congratulations to him!
8 9
ORAL PRESENTATIONS
PRACTICAL
Presenting authors of oral
INFORMATION communications are required to
bring their presentation on a USB
stick to the speaker ready room,
no later than the last coffee
WELCOME DESK CATERING TAXI break before their talk. Individual
Staff will be available to offer assistance Coffee will be served daily in Building 2, Should you need a taxi, please contact computers are not accepted.
with registration, city information and near the amphitheaters and the exhibition. the following companies:
transport. Opening hours : Lunches will be served daily as well, in a
Sunday: 9.30 - 19.00 dedicated room in Building 1. After lunch, Taxis 33: 05 56 74 95 06 POSTER SESSIONS
Monday: 08.00 - 18.30 you can enjoy a coffee or tea with sweets Taxis Alliance: 05 56 77 24 24
Tuesday: 08.00 - 18.30 during the poster sessions, in Building 2. Taxis Télé: 05 56 96 00 34 Two poster sessions are scheduled,
Wednesday: 08.00 - 16.00 Taxis Girondins: 05 56 80 70 37 on Monday and Tuesday after lunch
GALA DINNER (Building 2).
REGISTRATION FEE The gala dinner will be held on Tuesday Meeting point : main entrance Presenting authors are required to
Registration fee includes access to all the 16th of July, at Chateau Smith Haut ENSEIRB MATMECA / Bordeaux INP display their posters before Monday
sessions, conference material, daily coffee Lafitte, (Martillac). If you didn’t register for Avenue des Facultés at 12.00 (clips available on panels).
breaks, daily lunches, and the welcome the dinner, please see us at the welcome 33400 Talence
reception. The gala dinner is not included. desk. On-site registration will depend on The duration of the journey from the Authors of posters with even
last minute availabilities. If you chose the venue to the airport is +/- 30 minutes, numbers are required to present
NAME BADGE gala dinner option, a voucher has been depending on traffic. their paper during the poster
Please wear your badge at all times, inserted in your badge, please make sure session 1 on Monday.
including during the welcome reception. to present it at departure, scheduled at FREE PUBLIC TRANSPORT CARD Authors of posters with odd
For security reasons, badge controls may 18.45 from the venue. More info p.15 All participants have received a free numbers are required to present
be made during the symposium throughout travel card kindly offered by Bordeaux their paper during the poster
the venue. CLOAKROOM Métropôle. session 2 on Tuesday.
A secured cloakroom will be available in
WIRELESS INTERNET Building 1 for suitcases. We kindly ask These cards can be used for buses and Posters can be displayed during the
Free wireless internet is available you to keep valuable belongings like tramways in Bordeaux from the 14th to the whole duration of the symposium
throughout the venue. handbags and laptops with you. 17th of July. and must be taken down at the end,
on Wednesday.
Network: Bordeaux INP CERTIFICATE OF ATTENDANCE Please note that every time you use a
Password: a personal ID and password Certificates of attendance are provided route on the network, you must validate
are provided to each participant, written on on request at the welcome desk during your ticket, even if you are just changing POSTER AWARDS
the name badge. opening hours. services. Otherwise, you risk incurring a
hefty penalty. Poster prizes, sponsored by
Special instruction: If the connection is SPEAKER READY ROOM the Royal Society of Chemistry,
not automatic, please check if one of the The speaker ready room is located in BioTools and INITIO, FET Open
following security mechanisms is being the direct vicinity of the amphitheaters, in European Project, will be awarded
used: WPA2 Entreprise, AES, PEAP, Building 2. during the closing ceremony.
MSCHAPv2.
10 11
BORDEAUX
GENERAL INFORMATION
EMERGENCIES SHOPPING IN BORDEAUX
In France and in Bordeaux, stores are
In the event of a medical emergency: generally open from Monday to
(24 hours a day, 7 days a week) Saturday, from 10am to 7pm.
◆ Ambulance (Samu): 15 Essential shopping addresses in the
centre of Bordeaux are :
◆ Fire and rescue: 18
◆ SOS Médecins Bordeaux: 05 56 44 74 74
◆ Sainte-Catherine pedestrian street
◆ European Emergency Number: 112 (longest shopping street in Europe)
◆ Mollat book store (largest
Pharmacies open 24/7:
independent book store in France)
◆ Pharmacie des Capucins
◆ Quai des Marques (a group of factory
30 place des Capucins - Bordeaux
outlet stores and restaurants located
◆ Pharmacie d’Albret in former maritime warehouses of the
71 cours d’Albret - Bordeaux city, at the foot of the new bridge, Pont
Jacques Chaban Delmas)
Police : 17
◆ Mériadeck shopping centre (a large
Hôtel de Police - 23 rue François de Sourdis
downtown shopping centre with shops,
Tram line A - Hôtel de Police station
services and restaurants along with a
supermarket spanning 3 floors).
BORDEAUX PUBLIC TRANSPORT
Tramways run from 5am to midnight, Sunday to
SPECIAL EVENT IN BORDEAUX
Wednesday, and until 1am on Thursdays,
The French Republic National Day is
Fridays and Saturdays (last departures
celebrated on July 14th. This event
from terminal). During the day, tram services run
attracts millions of people each year in
every 3 to 5 minutes.The rest of the time, trams
a very festive atmosphere.
run every 8 to 15 minutes.
After the symposium welcome
Information and timetables
reception, we invite you to enjoy the
can be found on www.infotbm.com.
festive atmosphere of the Bordeaux
city and admire the traditional July 14th
BANK
fireworks, scheduled at 22.45, along
Most banks are closed on Sundays and
the Garonne river between the Pont de
Mondays, and are generally open from 9am to
Pierre and Place de la Bourse (subject
5pm. Cash machines can be found everywhere
to weather).
in town.
We advise you to leave your valuable
CURRENCY EXCHANGE
items and identity papers at your hotel,
Bureau de Change Novacambios Bordeaux
to avoid robberies. Please note that
46 cours du Chapeau rouge - Bordeaux
tram lines may be interrupted in the
very centre of Bordeaux during this
Tram line B - Grand Théâtre station
evening.
Opening hours: 10am - 7pm
13
12
© Bordeaux Convention Bureau
GALA DINNER The CHIRALITY 2019 gala dinner will take place at Château Smith Haut Lafitte, Grand cru
classé, one of the most famous and prestigious chateaux in the Bordeaux vineyards.
TUESDAY 16th JULY - 18.45 The gala dinner will be a great opportunity to exchange with the community in an exceptionnal
environment, and to taste the delicious Bordeaux wines.
PROGRAMME
18.45 Departure from the venue to Chateau
Smith Haut Lafitte (by bus)
Meeting point : see plan on p. 55
19.15 Arrival at Chateau Smith Haut Lafitte
19:20 Guided tour of the Smith Haut Lafitte estate
and wineries, following by a welcome cocktail
in the gardens (weather permitted).
20:40 Dinner served in the historical Cantelys Hall
23:00 Return journey to Bordeaux
23:30 Arrival at Bordeaux city centre
PLEASE NOTE:
The gala dinner is accessible by registration only
and costs extra.
If you took the gala dinner option during the registration
process, a voucher has been inserted in your badge.
Please make sure to present it at departure.
If you didn’t choose the gala dinner option, please note
that registration is subject to last minute availabilities
(information at the welcome desk).
Please also be aware that no return shuttle to Bordeaux
will be scheduled before the end of the dinner (around
23.00). Tramways run until midnight downtown.
14 15
THANK YOU PROGRAMME
TO OUR PARTNERS & SPONSORS SUNDAY 14th JULY
Time Amphitheater F
9.30 Welcome coffee
10.00 Short course 1: Chiroptical spectroscopy methods
for structural analysis of chiral molecules
Teachers:
Giovanna LONGHI, University of Brescia, Italy
Prasad POLAVARAPU, Vanderbilt University, USA
12.30 Lunch
13.30 Short courses 2 : Materials
Teachers:
Anja PALMANS, Eindhoven University of Technology, The Netherlands
Gil MARKOVICH, University of Tel Aviv, Israel
Amphitheater 1
16.00 Opening ceremony
Reiko ODA, Research director, Univ. of Bordeaux / CNRS / Bordeaux INP
Jeanne CRASSOUS, Research director, University of Rennes / CNRS
Jérôme LACOUR, Research director, University of Geneva, Switzerland
Philippe MORETTO, Vice president for Research, University of Bordeaux
Erick DUFOURC, Deputy Scientific Director, Institute of Chemistry (INC)
16.40 Chirality medal ceremony
16.50 Award lecture: Laurence A. NAFIE, Syracuse University, USA
Vibrational optical activity: discovery, development and future challenges
18.00 Welcome reception
20.00 End
16 17
PROGRAMME Plenary
Keynote
MONDAY 15th JULY AM Oral presentation AM
Time Amphitheater 1 Amphitheater 2 AM
8:45 Donald HILVERT, ETH Zurich, Switzerland Chair:
9:30 Design and evolution of artificial metalloenzymes K. Saigo
Polymer / materials 1 Spectroscopy 1
Chair: E. Hillard Chair: C. Merten
Eiji YASHIMA, Nagoya University, Japan
9:30 Giovanna LONGHI, University of Brescia, Italy
Control of macromolecular helicity for the
9:55 Circularly polarized luminescence of twisted conjugated systems
development of unique chiral materials
Tiziana BENINCORI, University of Insubria, Italy
9:55 Prasad POLAVARAPU, Vanderbilt University, USA
The «inherent chirality» concept: a very simple tool for designing materials
10:15 Dissymmetry factor spectral analysis can be a useful diastereomer discrimination tool
with impressive enantiodiscrimination ability
Xinhua WAN, Peking University, China
10:15 Christian JOHANNESSEN, University of Antwerp, Belgium
Induced circular dichroism of isotactic poly(2-vinylpyridine) with diverse
10:35 Resonance raman optical activity as a tool in structural biology: tales from the cold North
and tunable «sergeants-and-soldiers» type chiral amplification
Jochen BRANDT, Imperial College London, United Kingdom Tadashi MORI, Osaka University, Japan
10:35
Towards circularly polarized electroluminescence with Is there any meaningful correlation between emission and absorption
10:55
a high dissymmetry factor from chiral emitters dissymmetry factor values?
Coffee break Coffee break
Fundamentals Supramolecular 1
Chair: V. Rodriguez Chair: E. Yashima
11:15 Cornelia MEINERT, University of Côte d’Azur, France
Jay SIEGEL, Tianjin University, China
11:40 The Asymmetry of life
Chirality and corannulene
Yukata OKAZAKI, Kyoto University, Japan
11:40 Eric GRELET, CRPP, University of Bordeaux, France
Detection of chiralized monoatomic anions using molecular assembled nanohelices as
12:00 Chirality-controlled self-assembly via topological defects
UV-transparent chiral template
Donato MONTI, University of Rome Tor Vergata, Italy
12:00 Maxwell CROSSLEY, University of Sydney, Australia
Supramolecular chirality and morphological features of homo and
12:20 The last fundamental form of stereoisomerism revealed !
heteroaggregates of zinc (l)- and (d)-proline-porphyrin derivatives.
12:20 David GONZALEZ RODRIGUEZ, University of Madrid, Spain
Oliver TRAPP, Ludwig-Maximilians University, Germany *
12:40 Helically chiral self-assembled nanotubes through hierarchical
Emergence of evolution and homochirality on a molecular level
12:45* coupling of cooperative interactions
Lunch Lunch
18 19PROGRAMME Plenary
Keynote
MONDAY 15th JULY PM Oral presentation PM
13:30
Poster session 1 (even numbers) Poster session 1 (even numbers)
14:50
Time Amphitheater 1 Amphitheater 2
Asymmetric 1 Chirality at nano 1
Chair : J. Canary Chair : B. Kauffmann
Shinobu TAKISAWA, Osaka University, Japan Gil MARKOVICH, Tel Aviv University, Israel
14:50
Facile enantioselective synthesis of hetero[9]helicenes Spontaneous and directed symmetry breaking in the formation
15:10
using redox/acid cooperative catalysts of chiral lanthanide phosphate nanocrystals
Jon ANTILLA, Tianjin University, China Zhifeng HUANG, Hong Kong Baptist University, China
15:10
Chiral phosphoric acid and metal chiral phosphate catalysis: double asymmetric Intrinsically chiral nanoparticles with sub-10 nm pitch:
15:30
catalytic reaction (dacr) and the arylation of indolyl methanols fabrication, characterization and applications
Francesco TASSINARI, Weizmann Institute of Science, Israel Andrew GELLMAN, Carnegie Mellon University, USA
15:30
Enantioselective reduction of camphorsulphonic acid Surface structure sensitive enantioselectivity:
15:50
using a spin-polarized electrode quantification across chiral surface orientations
Joanna WENCEL-DELORD, University of Strasbourg, France Shunai CHE, Shangaï Jiao Tong University, China
15:50 Sulfoxide as a new solution for accessing original chiral molecules Chirally mesostructured inorganic materials with optical activity
16:15 via C-H activation
Coffee break Coffee break
Supramolecular (bio) Physical computational
Chair: G. Guichard Chair: T. Asahi
Lucile FISCHER, University of Bordeaux, France
16:35 Inbal TUVI-ARAD, The Open University of Israel
Chirality induction in oligoamide aromatic foldamers interacting
16:55 Protein chirality spectrum and chiral ramachandran plots
with protein surfaces
Nathan VAN ZEE, Eindhoven University of Technology, The Netherlands
16:55 Jiri KESSLER, Czech Academy of Sciences, Czech Republic
Exploiting monomeric water in apolar environments to control the structure
17:15 Modeling of resonance-induced enhancement of solvent raman optical activity
of supramolecular polymers
17:15 Jonathan CLAYDEN, University of Bristol, United Kingdom* Shira YOCHELIS, The Hebrew University of Jerusalem, Israel
17:35 Communicating chirality using molecular conformation Chirality and the electron spin
17:40*
Michinori SUGINOME, Kyoto University, Japan Chair:
17:40
Asymmetric catalysis with chirality-amplifiable N. Berova
18:35
dynamic helical macromolecular catalysts
Free evening Free evening
20 21Plenary
PROGRAMME Keynote
TUESDAY 16th JULY AM Oral presentation AM
Time Amphitheater 1 Amphitheater 2
8:45 Virginie SIMONET, CNRS / Grenoble Alpes University, France
9:30 Magnetic chirality Chair: P. Rosa
Supramolecular 2 Chiral resolution
Chair: D. Walba Chair: C. Welch
Jérôme LACOUR, University of Geneva, Switzerland Jun SHEN, Harbin Engineering University, China
9:30
Supramolecular chemistry and chiroptical spectroscopy Controlled synthesis and enantioseparation ability of polysaccharide
9:55
of readily prepared chiral macrocycles derivatives bearing various functional pendants
Minghua LIU, Institute of Chemistry, China
9:55 Reiko KURODA, Chubu University, Japan
Circularly polarized luminescence from supramolecular nanoassemblies
10:15 Spontaneous optical resolution in the crystalline state
of pi-conjugated gelators
Yann MAIRESSE, University of Bordeaux, France
10:15 Stephen GOLDUP, University of Southampton, United Kingdom
Real-time determination of enantiomeric and isomeric content
10:35 Mechanical chirality and mechanical motion
using photoelectron elliptical dichroism
Chunhong ZHANG, Harbin Engineering University, China
10:35 Aya TANATANI, Ochanomizu University, Japan
Synthesis of helical poly(phenylacetylene)s bearing l-proline dipeptide derivatives
10:55 Development of helical structures based on the aromatic squaramides
with different sequences as pendants and their chiral recognition abilities
Coffee break Coffee break
Spectroscopy 2 Asymmetric 2
Chair: L. Guy Chair: S. Nlate
Chiara CAPPELLI, Scuola Normale Superiore, Italy
11:15 Jieping ZHU, EPFL, Switzerland
A fully polarizable embedding model for chiroptical spectroscopy
11:40 Ion-pairing in catalytic enantioselective rearrangements
of complexsystems: status and perspectives
Christian MERTEN, Ruhr-University Bochum, Germany Takanori SHIBATA, Waseda University, Japan
11:40
VCD spectroscopy as tool to investigate substrate binding Enantioselective construction of saddle-shaped chirality in
12:00
in asymmetric catalysts benzene-fused heteroatom-containing medium ring systems
Reilly SONSTROM, University of Virginia, USA Christophe MICHON, University of Lille, France
12:00
Chiral analysis of molecules with multiple chiral center Development of chiral C2-Symmetric N-Heterocyclic carbene Rh(I) catalysts through
* Registration mandatory
12:20
using chiral tag rotational spectroscopy control of their steric properties
12:20 Lorenzo DI BARI, University of Pisa, Italy* Erika BENEDETTI, Paris Descartes University, France
12:40 Discrimination of circularly polarized light based on molecular, Highly enantioselective asymmetric transfer hydrogenation: a practical
12:45* supramolecular and mesoscopic chirality and scalable method to efficiently access planar chiral [2.2]paracyclophanes
22 Lunch Vendor Lunch* Lunch Vendor Lunch* 23Plenary
PROGRAMME Keynote
TUESDAY 16th JULY PM Oral presentation PM
13:45
Poster session 2 (odd numbers) Poster session 2 (odd numbers)
14:50
Time Amphitheater 1 Amphitheater 2
Asymmetric 3 Polymer / materials 2
Chair: J. Lacour Chair: N. Avarvari
Keiji MARUOKA, Kyoto University, Japan
14:50 Anja PALMANS Eindhoven University, The Netherlands
Design of new, high-performance organocatalysts
15:15 From molecular to supramolecular chirality and back
with privileged structures for asymmetric catalysis
Timothée CADART, Charles University, Czech Republic
15:15 Max HIRSCHMANN, Technische Universität Darmstadt, Germany
Synthesis of enantioenriched helical bispiroindeno[2,1-c]fluorenes
15:35 Thermo- and magnetoresponsive polyaspartates
via an enantioselective [2+2+2] cyclotrimerization step
Mohamed AMEDJKOUH, University of Oslo, Norway Girish LAKHWANI, University of Sydney, Australia
15:35
Remote asymmetric amplification in synergistic Hierarchical self-assembly of chiral Perylene Imide based
15:55
and responsive autocatalytic systems organogelators explained
Marine MICHEL, Imperial College London, United Kingdom
15:55 Yannick GEIGER, IPCM Strasbourg, France
Enantioselective polymeric membranes for chiral separation:
16:15 First observation of hyperpositive non-linear effects in asymmetric catalysis
comparison of pressure driven separation, pertraction and preferential sorption
Coffee break Coffee break
Enantioseparation Chirality at Nano 2
Chair: C. Villani Chair: E. Pouget
16:35 Pilar FRANCO, Chiral Technologies, France Nathalie KATSONIS University of Twente, The Netherlands
17:00 Chirality in chromatography: where should innovation go ? Chirality-derived motion of protocells
17:00 Ashraf GHANEM, University of Canberra, Australia Davy GERARD, University of Troyes, France
17:20 Chirality at the dried blood spot: enantioselective analysis of pharmaceuticals Probing optical chirality in the near-field of plasmonic nanostructures
on sub two micron columns with photosensitive azobenzene-containing polymers
Ben SLATER, Imperial College London, United Kingdom
17:20 Ventsislav VALEV, University of Bath, United Kingdom
Mechanistic detail of enantioselective adsorption
17:40 First observation of optical activity in hyper-rayleigh scattering
in a chiral metal organic framework
KENJI HAMASE, Kyushu University, Japan
17:40 Ignacio GARZON, University of Mexico, Mexico
Multi-dimensional HPLC analysis of chiral α-amino acids
18:00 Chirality in bare and ligand-protected metal nanoparticles
and carboxylic acids in extraterrestrial materials
Zachary BREITBACH, AbbVie Inc., USA Hirotaka IHARA, University of Kumamoto, Japan
18:00 Evaluation of newly commercialized sub-2 µm chiral stationary phases Strong and tunable circularly polarized luminescence induced
18:25 in SFC and HPLC by chiral supramolecular gel
18:45 Departure for gala dinner at Chateau Smith Haut Lafitte Departure for gala dinner at Chateau Smith Haut Lafitte
24 25PROGRAMME Plenary
WEDNESDAY 17th JULY
Keynote
AM Oral presentation AM
Time Amphitheater 1 Amphitheater 2
8:45 Nicholas KOTOV, University of Michigan, USA Chair:
9:30 Chiral Inorganic Nanostructures W. Lindner
Spectroscopy 3 Polymer / Materials 3
Chair: L. Di Bari Chair: I. Azumaya
9:30 Petr BOUR, University of Prague, Czech Republic
Narcis AVARVARI, University of Angers, France
9:55 Interpretation of optical activity spectra of proteins
Chiral materials based on tetrathiafulvalene and metal-dithiolene complexes
Wada TAKEHIKO, Tohoku University, Japan
Karl-Heinz ERNST, Swiss Federal Laboratories for Materials Science and
9:55 Development of high sensitive and high time-resolved circular dichroism (CD)
Technology, Switzerland
10:15 measurement system “Toward the analyses of biomolecular interactions and
On-surface topochemistry of helicenes
their dynamics“
Anne ZEHNACKER, Institut des Sciences Moléculaires d’Orsay, France
10:15 Félix FREIRE, University of Santiago de Compostela, Spain
Vibrational circular dichroism study of the solid-state organisation of ring-
10:35 Sergeants and soldiers effect in chiral dynamic helical copolymers
containing peptides
Sergio ABBATE, University of Brescia, Italy Katsuhiro MAEDA, Kanazawa University, Japan
10:35
How to deal with anharmonicities in various circumstances to obtain safe Synthesis of a single-handed helical poly(diphenylacetylene) derivative based on
10:55
conformational and configurational information from VCD spectra helicity induction and memory effect and its conformational analysis
Coffee break Coffee break
Supramolecular 4 Asymmetric 4
Chair: T. Brotin Chair: Y. Landais
Tsuneomi KAWASAKI, Tokyo University of Science, Japan
11:15 Ji-Young KIM, University of Michigan, USA
Asymmetric Strecker-type synthesis by using chiral amine arising from hydrogen
11:35 Circularly polarized light driven chiral assembly of gold nanoparticles
isotope substitution
11:35 Stéphane LE GAC, University of Rennes 1, France Wim NOORDUIN, AMOLF Institute, The Netherlands
12:00 Towards chiroptical sensing from Möbius-type receptors Physicochemical routes to enantiomeric purity
Kazushi KINBARA, Tokyo Institute of Technology, Japan
12:00 Takeo KAWABATA, Kyoto University, Japan
Design of synthetic chiral receptor molecules inspired
12:20 5Å-Hypothesis for remote asymmetric induction
by structure and function of membrane proteins
12:20 Matthieu RAYNAL, Sorbonne University, France
Stephen FLETCHER, University of Oxford, United Kingdom*
12:40 Dynamic asymmetric catalysis by tuning the structure
Asymmetric additions to racemates
12:45* of supramolecular helices
Lunch Lunch
26 27PROGRAMME POSTER
WEDNESDAY 17th JULY PM SESSIONS
Time Amphitheater 1 POSTER N° AUTHOR TITLE
Chair: O.Trapp Controlling the preferential motion of chiral molecular
P1 Abbasi David
walkers on a surface
13:45 Yunjie XU, University of Alberta, Canada CD and CPL spectra of pyrenopyrene-based helicene
P2 Abbate Sergio
hybrids
14:30 Conformational landscapes and non-covalent interactions
of chiral molecules: chirality recognition/transfer/amplification TetraPh-Tol-BITIOPO: a new atropisomeric
3,3’-bithiophene based phosphane oxide as
P3 Abbinante Vincenzo Mirco
organocatalyst in lewis base-catalyzed lewis acid
mediated reactions
14:30 Alexander KUHN, University of Bordeaux / CNRS / Bordeaux INP, France
Miniemulsion polymerization of chiral nanoparticles of
15:15 Chiral biomimetic metal electrodes for enantioselective analysis, P4 Abuaf Meir amino acid and their application for enantioselective
separation and synthesis separation
Synthesis of polyacetylene derivatives bearing axially
P5 Ando Mitsuka chiral pendants and their application to asymmetric
15:15 Poster awards - Closing remarks catalysis
16:00 Presentation of CHIRALITY 2020 P6 Andrushchenko Valery Supramolecular chirality of nucleic acids
Enantioseparation of the four nadolol stereoisomers by
P7 Arafah Rami
fixed-bed and simulated moving bed chromatography
End Synthesis and evaluation of chiral spirooxindoles for
P8 Arai Midori
Notch signal inhibitors
Actual iodinating reagent in catalytic asymmetric halo-
P9 Arai Takayoshi
lactonization
Viedma ripening: a simple access to enantiomerically
P10 Baglai Iaroslav
pure compounds
P11 Baguenard Bruno Fast circularly polarized luminescence spectroscopy
VCD spectral markers of acetonide rings: facilitating
P12 Batista Jr. Joao M.
absolute configuration assignments of diols
Chiroptical redox switching of tetra-cationic derivatives
P13 Bednarova Lucie
of azoniahelicenes
The first hexahelicene-substituted tetrapyrrole:
P14 Belviso Sandra synthesis, HPLC enantiomeric separation, and
absolute configuration
P15 Blasius Jan New approaches for calculating VCD spectra
3D imaging of dichroism in the photoionization of chiral
P16 Bloch Etienne
molecules by ultrashort laser pulses
Sensitive analysis of chiral pharmaceuticals by
P17 Bond Caoimhe
photoelectron spectroscopy
Synthesis of meso oligourea foldamers built from chiral
P18 Bornerie Mégane
subunits
P19 Bosson Johann Late-stage functionalizations of cationic helicenes
28 29POSTER POSTER
SESSIONS SESSIONS
Photo-tunable aromatic oligoamide foldamers for Chiral gold nanoparticle superstructures directed by
P20 Boulloy Alice
controlled carbohydrate encapsulation P39 Gao Jie silica nanohelices towards innovative chiro-optical
properties
Computing bulk phase vcd and roa spectra from ab
P21 Brehm Martin
initio molecular dynamics Circularly polarized phosphorescent chirality-at-
rhenium complexes bearing a helicenic NHC ligand
Chiroptical properties of water-soluble cryptophane P40 Gauthier Etienne
P22 Brotin Thierry : studies of their chiroptical and photophysical
derivatives and their complexes
properties.
Kinetic investigation of chiral nanometric molecular
Enantioselective carbocyclization reactions catalyzed
P23 Buffeteau Thierry assemblies by electronic (ECD) and vibrational (VCD)
P41 Gicquiaud Julien by Brönsted acids involving carbon-carbon triple bond
circular dichroisms
activation.
Synthesis of novel nicotinamide-attached binol
P24 Choi Yunjeong Exploring the versatility of chiral molecules in crystals
receptor as chiral shift reagent for amino acids P42 Giorgi Michel
by combining XRD and CD
Flow reactors based on supported 9-amino-9-deoxy-
Enantio- and diastereoselective Suzuki-Miyaura
P25 Ciogli Alessia 9-epi-quinine for stereoselective activation of carbonyl P43 Goetzke Wieland
coupling with racemic bicycles
compounds
Asymmetric synthesis of acyclic pyrimidine nucleosides
Design and preparation of new chiral atropisomeric P44 Ha Heun-Jong
by organocatalytic aza-Michael reaction
P26 Clavier Hervé N-heterocyclic carbene ligands: application in
asymmetric catalysis Stereodivergent synthesis by means of chirally ampli-
P45 Hammoud Ahmad
fied supramolecular catalysts
Unidirectional rotation in molecular motors with
P27 Costil Romain
a helically chiral rotor Organocatalytic umpolung Michael process: synthesis
P46 Hanatani Yutaro of highly functionalized ketones bearing a chiral
Vibrational optical activity and induced solvent ROA of
P28 Daugey Nicolas quaternary carbon center
chiral trinuclear paddlewheel complexes
Tunable P-stereogenic P,N-Heterobidentate Ligand/
Whisky lactone : new chiral separation and chiroptical
P29 Daugey Nicolas P47 Hérault Damien Pd(II) Complexes: Synthesis, Characterization and
identification
Enantioselective Catalysis
Conversion of axial-to-central chirality of heteroarene
P30 Devaraj Karthik Chiral symmetry breaking of spiropyrans and
atropisomers
P48 Hiroki Ishikawa spirooxazines via dynamic enantioselective
Circularly polarized luminescence of novel chiral heli- crystallization
P31 Dhbaibi Kais
cene molecules
Temperature dependent chirality recognition of
Effect of crosslinker on chiral separation of surface mo- P49 Hirose Keiji rotaxane hosts having chirality specific to rotaxane
P32 Dong Hongxing
lecularly imprinted polymer as chiral stationary phase structure in complexation with chiral guests
P33 Durola Fabien Rigid twisted chiral conjugated macrocycles Combined (+/-) ECD and (on/off) CPL reversible swit-
P50 Homberg Alexandre
Helical push-pull dyes with intense circularly polarized ching with chiral fluorescent polyether macrocycles
P34 Favereau Ludovic
(CP) luminescence for CP-organic light emitting diodes Induced circular dichroism of phenol complexes with
P51 Hong Aram
P35 Fernandez Zulema Chiral Harvesting in POPEAs chiral molecules in a supersonic jet
Helically-chiral poly(isocyanides) as asymmetric transi- Design and development of a highly selective chiral
P36 Fleckenstein Max 3D-HPLC system for the determination of lactate and
tion metal catalysts P52 Hsieh Chin-Ling
3-Hydroxybutyrate enantiomers in human physiological
Multiscale chirality and symmetry in the supramolecular fluids
P37 Fossépré Mathieu
self-assembly of DNA with a �-conjugated polymer
Histidine-metal complexes studied by spectroscopic
Synthesis of a helix-sense switchable poly(phenyl P53 Hudecova Jana
and computational methods
isocyanate) derivative bearing a stimuli-responsive
P38 Fukuda Mayu Sub-2-Micron stationary phase innovations rise to
optically active group at the initial chain end and its
chiroptical properties meet the demands of modern chromatographer, a
P54 Ibrahim Diana
comparative study between two columns: Chiralpak®
IG-U and Chiralpak® ID-U
30 31POSTER POSTER
SESSIONS SESSIONS
Analysis of cannabidiol in CBD products by SFC-CD- DFT calculation of chiroptical and NMR data for distin-
P55 Iijima Satoe P73 Kurtan Tibor
MS guishing stereoisomeric natural products
Side chain-driven bimodal helical conformation of non- Chiral assembling of metal complexes induced by
P56 Ishido Yuki P74 Kuwahara Yutaka
natural polypeptide derived from arylene ring flips glutamide substituted pyridinium salts
Chiral polymers of cinchona alkaloid derivatives for Silylium Ions with si-centered chirality - chiral memory
P57 Itsuno Shinichi P75 Laye Claire
asymmetric organocatalysts at silicon
Separation of racemic mixtures by non-porous The increase of lactate enantiomers in the serum and
P58 Izak Pavel P76 Lee Jen-Ai
membranes urine of mice with nephrotoxic serum nephritis
A spectroscopic study of the formic acid - hydrogen Crystallization-induced diastereomer transformation of
P59 Jaeger Wolfgang
peroxide complex: signatures of transient chirality P77 Lerdwiriyanupap Tharit N-[(S)-1-phenylethyl]-(D/L)-mandelamide through the
phase transformation
Novel Poly(2-oxazoline)s bearing triazolylpyrrolidine
P60 Jiang Liming pendants for asymmetric catalysis of the michael Lamellar-twisting-induced electronic circular dichroism
P78 Li Ming-Chia
addition in water of chromophore moieties in banded spherulites
Development of chiral crown ether type column for Chirality induced from inorganic silica nanohelices
P61 Jin Jong Sung P79 Liu Peizhao
optical resolution of racemic drugs with amino group templates to inorganic perovskites nanocrystals
Enantioselective resolution of racemic amino acids by Chiral communications in a three-level chirality totem.
P62 Jin Yingji liquid-liquid extraction using chiral extractors with tert- P80 Ménand Mickaël remote-control of the möbius aromatic twisting in
butyl ketone group hexaphyrin-cyclodextrin hybrids
Thermo-induced chirality change of supramolecular Fabrication of conductive nanohelix by electrochemical
P63 Jintoku Hirokuni P81 Maeda Yuki
assembly in polymer matrix filling of helical nanopores in silicon
Asymmetric Suzuki-Miyaura cross-coupling reactions Fabrication of hybrid chiral hydrogels composed of 1D
P82 Makoto Takafuji
P64 Kamiya Naoaki in aqueous media by using water-soluble helical self-assembly crosslinked-polymer network
polymer ligands
Vibrational circular dichroism reveals supramolecular
Chirality-controlled synthesis of double-helical au P83 Martial Benjamin chirality inversion of α-synuclein peptide assemblies
P65 Kawai Takeshi
nanowires upon interactions with anionic membranes
Self-replication of chiral α-hydroxy acids in the Strec- Mechanistic study of asymmetric autocatalysis using
ker-type synthesis in combination with asymmetric P84 Matsumoto Arimasa cd spectrum: temperature and concentration effect on
P66 Kawasaki Tsuneomi
amplification of chiral intermediate cyanohydrin in catalysts aggregation structure
solid-state
Triphenylmethyl radical-based halogenated derivatives:
Enantioselective Strecker-type amino acids synthesis P85 Mayorga-Burrezo Paula where luminiscence, magnetism and chirality gracefully
P67 Kawasaki Tsuneomi by using chiral crystal of racemic cyanohydrin as a coexist.
substrate and source of chirality
Intramolecularly interlocked stereodynamic catalysts: a
P86 Menke Jan-Michael
Stereoselective synthesis of carboxy-substituted new concept to excellent enantioselectivity
P68 Kim Bora 2-isoxazolines by phase-transfer-catalyzed cascade
Raman optical activity of intermolecular, overtone and
reaction P87 Michal Pavel
combination bands, and absolute spectral intensities
Helical inversion of peptide-based supramolecular
P69 Kim Ka Young Circularly polarized selective reflection from achiral
polymer
P88 Nagata Yuuya poly(quinoxaline-2,3-diyl)s forming cholesteric su-
Supramolecular chirality by light-induced self-assembly perstructure by the exposure of vapor of chiral solvents
P70 Kim Sang Youl
of achiral triphenylamine molecules
Synthesis and application of novel photoswitchable
P89 Nakamura Kento
Preparation of condensed chiral O- and O,N-heterocy- chiral catalyst
P71 Kiraly Sandor Balazs
cles in diastereoselective domino reactions
Chiral gold nanoparticles synthesized in chiral
Chiral and fluorescent dynamic covalent polymers for P90 Nakaya Masahiro nanospace constructed by molecular assembled
P72 Kotras Clément
DNA complexation nanohelices
32 33POSTER POSTER
SESSIONS SESSIONS
Rapid characterization of enantiomeric excess using Diazirine 14N/15N isotopomers: chirality and hyperpo-
P91 Neill Justin P109 Reboul Vincent
molecular rotational resonance spectroscopy larization
Asymmetrically substituted poly(diphenylacetylene)s Photoelectron circular dichroism observed on the
P110 Ring Tom
bearing a chiral pendant through an amide linkage that nanosecond timescale
P92 Nozaki Mai
exhibit solvent-dependent helicity inversion and their
Competing stereocenters defining the helical sense of
chiral recognition abilities P111 Rivadulla Elena
polymers
The influence of chiral additives on separation of
P93 Nulek Thitapond Elastin-based helical polymers: custom-made chiro-
aspartic acid P112 Rodriguez Rafael
fluorescent materials with biological applications
Helically chiral poly(quinoxaline-2,3-diyl)s bearing
P94 Ogita Takuya The use of UiO-type MOFs in vapour phase Soai
N-heterocyclic carbene pendants P113 Rotunno Giuseppe
reactions
Synthesis of macrocycles bearing dynamic helical
P95 Okutsu Hinako Chiral discrimination by enantioselective raman spec-
peptide chains and their chiroptical properties P114 Rullich Claudia
troscopy and chemometric approaches
Aromatic oligoamide foldamers as versatile scaffolds
P115 Ryoo Jae Jeong Ultrasound-controlled chiral separation
P96 Olivier Céline for induced circularly polarized luminescence at adjus-
table wavelengths Chirality induction in rare earth-silica nanohybrids
P116 Ryu Naoya prepared by templating amphiphile-dye supramolecular
Functionalization of ethynyl [4]helicenes through diels-
assemblies
P97 Ondrisek Pavol alder-retro-diels-alder reactions. investigation of the
resulting atropisomeric situation Chiral guest recognition behaviour of a pentanuclear
P117 Sakata Yoko metallonanobelt constructed by template-directed
Stereocontrol of planar-chiral bridged isonicotinamide
P98 Ono Ryutaro self-assembly of a triptycene-based ligand
via crystallization-induced asymmetric transformation
Effects on enantiomeric resolutions of chiral pesticides
Time-resolved broadband circular dichroism in the
P99 Oppermann Malte P118 Salafia Fabio through different conditions of supercritical fluid chro-
deep-UV
matography
Asymmetric induction of Wulfingite chiral crystals
P100 Otis Gil Comparison of monodimensional and multidimensional
detected using EPR spectroscopy
P119 Salafia Fabio gas chromatography methods for the separation of
Design and synthesis of chiral peptide polymers for volatile chiral compounds in mandarin essential oil
P101 Ouyang Jiangkun
information storage
BenzoDiazepinoIndoliums: novel class of chiral polycy-
P120 Saleh Nidal
Critical role of achiral guest molecules in planar chira- clic fluorophores
P102 Park Jaehyeon
lity in-version of alanine-appended pillar[5]arenes
Exploring pathway complexity in chiral supramolecular
P121 Sallembien Quentin
Optically active flexible materials based on molecular polymers reveals a thermo-thickening effect
P103 Pathan Shaheen
assembly template chiral hybrid nanostructures
Role of electric field on enantio-specific interactions of
P122 Santra Kakali
Organocatalytic synthesis of chiral spirocyclopentene chiral molecules with ferromagnetic substrates
P104 Perrio Stephane oxindole derivatives through a sulfinate ammonium ion
Grafting of organics fluorophores on chiral hybrid
pair P123 Scalabre Antoine
nanostructures
Chiroptical super-spectra of Co(II) salicylaldiminato
Enantiospecific interactions of propylene oxide with
P105 Pescitelli Gennaro complexes with symmetry-dependent vibrational circu- P124 Shukla Nisha
penicillamine
lar dichroism enhancement
Bio-orthogonal single chain polymeric nanoparticle
Pressure-induced conformational change of a dipep- P125 Sklorz Julian
P106 Plamitzer Lubos catalyse cyclopropanation
tide. a computational study
Resolution of flecainide and its derivatives, an antiar-
Polavarapu Lakshmina- Chiral perovskite nanocrystals: chirality transfer from
P107 P126 Sung Ji Yeong rhythmic agent that treats abnormal heart rhythms, on
rayana ligand molecules to excitons
a new chiral stationary phase
Chirality and anion size driven properties of methylated
P108 Pop Flavia Biphenyl chiroptical probes as tools for the assignment
EDT-TTF conductors P127 Superchi Stefano
of absolute configuration to natural products
34 35POSTER POSTER
SESSIONS SESSIONS
Regio- and stereoselective tandem carbolithia- Enantiopure encaged Verkade’s superbases:
P128 Superchi Stefano
tion-substitution reaction on 1-aryl-vinylcarbamates P148 Yang Jian synthesis, chiroptical properties, and use as chiral
derivatizing agent
DNA-induced chirality in templated supramolecular
P129 Surin Mathieu
assemblies of conjugated molecules Effect of shapes of pt nanoparticles on helical nano-
P149 Yasuda Takumi pores formed by metal-assisted chemical etching of
Enantioselective O- to C- Acyl rearrangement of
silicon
P130 Takahashi Takuya oxindole derivatives using helically chiral nucleophilic
polymer catalyst Quantitative resolution of conglomerates through a
P150 Ye Xichong
magnetic separation strategy
Rapid and comprehensive determination of absolute
configurations of a series of natural bitter compounds Hierarchically chiral inorganic films with multi-optical
P131 Taniguchi Yoshimasa P151 Yingying Duan
derived from hop (humulus lupulus l.) by the crystalline activities
sponge method
Generation of room-temperature phosphoresce based
P132 Tassoni Alessandra Chiral resolution using circular Couette flow P152 Yoshida Kyohei on one-dimensional chiral stacking of a simple lumino-
phore
Separation and chiroptical properties of chiral
P133 Teeuwen Paula
porphyrin cages CPL switching system utilizing microgel of pNIPAM
P153 Yoshida Kyohei
P134 Thinhinane Aoudjit Nanoscale photoimaging of chiral nanostructures functionalized by Ru(bpy)3 and phenylbornic acid
Stereocontrolled access to all-carbon quaternary Catalytic asymmetric umpolung organocascade
P135 Traboulsi Iman stereocenter in cyclic and acyclic systems. approach to P154 Yoshida Yasushi
reaction of α-imino carbonyl compounds
the total synthesis of indole alkaloids.
Supramolecular asymmetric photochirogenesis of
Absolute asymmetric synthesis by diels-alder reaction P155 Yospanya Wijak 2-anthracene carboxylate dimers in chiral medias: from
P136 Uemura Naohiro
involving dynamic enantioselective crystallization synthetic antibodies to silica hybrid nanofibers
Exotic techniques for the characterization of chirality: Investigation of chirality-dependent growth of
P137 Valentin-Pérez Angela P156 Zelenovskii Pavel
x-ray natural circular dichroism diphenylalanine microtubes
New chiral iodoarenes and iodanes for asymmetric Chirality induction of inorganic-organic hybrid assem-
P138 Valzer Emmanuel P157 Zhang Jie
C-O and C-C bondforming reactions bled materials
Controlling the length of cooperative helical
P139 Vantomme Ghislaine Utilizing chiral induced spin selectivity effect to enantio-
supramolecular polymers P158 Metzger Tzuriel S.
separation
Compression of supercontinuum pulses using different
P140 Vasudevan Sudheendran
chirped mirror technologies
Development of helical aromatic oligoamides based on
Intensity-dependent hyper-rayleigh chiroptical effect P159 Tanatani Aya
conformational property of aromatic tertiary amide
P141 Verreault Dominique in liquids: a new route for the determination of the
enantiomeric excess Penélope Rodríguez- Effect of metal core on chiroptical activity of L- and
P161
First chiral discrimination of helical oligoquinoline Zamora D-Cysteine protected nanoparticles
P142 Verreault Dominique foldamers in solution evidenced by hyper-rayleigh
scattering P162 Laureen Moreaud Programmed artificial protein origami super-helix
P143 Vidanović Igor Modification of bicyclic ketones for PECD experiments
Chromatographic resolution and absolute configuration
P144 Villani Claudio
determination of stereolabile indole derivatives
P145 Wada Yuya Triptycene-based chiral functional molecules/polymers Authors of posters with even numbers are required to present their paper during the poster
Synthesis of spiroborate-based homo and hetero session 1 on Monday. Authors of posters with odd numbers are required to present their
P146 Xiang Wang
double-strand helicates paper during the poster session 2 on Tuesday.
Circularly polarized luminescence (CPL) activities in
P147 Yamana Kazushige
helical assemblies of pyrenes on RNA Duplex
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WATER TECHNOLOGIESPROGRAMME VENUE
OVERVIEW
TIME* Sunday 14th July Monday 15th July Tuesday 16th July Wed. 17th July Amphitheater 2 Coffee break
08.00 floor -1
aera
08.30 Meeting point
Plenary session Plenary session Plenary session gala dinner
09.00 Poster Poster
sessions sessions
09.30
10.00 Sponsors
Speaker exhibition
10.30
Parallel sessions Parallel sessions Parallel sessions ready room
11.00
Short course 1
11.30
Information ^
desk Please, wear your
12.00 badge at all times.
12.30 BUILDING 2 Amphitheater 1
Lunch Lunch Lunch
13.00
Lunch Cloakroom
13.30
Poster session 1 Poster session 2 Plenary session
14.00
(even numbers) (odd numbers)
14.30
Short course 2 Plenary session
15.00
15.30 Poster awards
16.00 Closing remarks
16.30 Opening ceremony
Parallel sessions Parallel sessions Lunch area
17.00 Chirality Medal BUILDING 1
Welcome
17.30
desk
18.00
18.30
19.00 Welcome
reception Gala dinner
19.30 Chateau Smith ^
Haut Lafitte** Main entrance
20.00
*Approximate time - Please check the detailed programme.
** Departure : 18:45 from the venue - End: 23.00
Taxi meeting point
ENSEIRB MATMECA
>
Arts et métiers
Avenue des Facultés tramway station
54 Talence
55Chirality 2019
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