POSTER
SESSIONS
Monday, 12
Sept.,
Afternoon
14.00-15.00
SESSION A
Fac. of
Engineering
P1.
New
chiral Mn(III)salen complex covalently bonded to modified SBA-15 and
MCM-41 as
efficient heterogeneous catalysts for synthesis of fine chemicals and
pharmaceutical important chiral
epoxides
I. Ahmad, R. I. Kureshy, N. H. Khan, S. H. R. Abdi, S.
Singh, R.V.
Jasra, Central Salt & Marine Chemical Research Institute,
Bhavnagar ( Gujarat), India
P2.
Acid
catalyzed racemization process of atropisomeric N-aryl o-substituted
thiazoline thiones
F. Andreoli, N. Vanthuyne, C. Roussel, Paul Cézanne
University, UMR Chirotechnologies, Marseille, France
P3.
New
chiral
capsules formed by the self-assembly of N,C-linked peptidocalix[4]arene
L. Baldini, G. Faimani, F. Guerrini, F. Vignali, A. Casnati, F.
Sansone,
R. Ungaro, Dip. di Chimica Organica e Industriale, Universitŕ di
Parma,
Parma, Italy
P4.
Design,
synthesis and NMR analysis of Phosphorus containing derivatives of
quinine as
receptors of N-benzyloxycarbonyl-amino acids
Ł. Berlicki, P. Młynarz, P. Kafarski, Dept. of Bioorganic
Chemistry, Wrocław University of Technology, Wrocław, Poland
P5.
Chiral
interactions of short peptides in stirred
crystallization
T. Berman, Y. Mastai, Dept. of Chemistry Bar-Ilan
University, Ramat-Gan, Israel
P6.
Heterogeneous
asymmetric epoxidation of olefins catalysed by (salen)Mn(III) complex
singly-bounded to
silica
F. Bigi, G. Fiorino, G. Sartori, Dip. di
Chimica Organica e Industriale,
Universitŕ di Parma, Parma, Italy
P7.
Peculiarities
of supramolecular chirogenesis with bis-chlorin hosts
V. V. Borovkov, Y. Inoue, Entropy Control Project, ICORP,
JST, Osaka,
Japan
P8.
Chiral
recognition studies by chiral basket-resorc[4]arene receptors
B. Botta, L. Nevola, I. D’Acquarica, G. Delle Monache, D.
Subissati, G.
Zappia, D. Misiti, Dip. Studi di Chimica e Tecnologia delle
Sostanze
Biologicamente Attive, Universitŕ "La Sapienza", Roma, & Ist. di
Chimica Farmaceutica, Universitŕ degli Studi di Urbino "Carlo Bo",
Urbino, Italy
P9.
Gas
chromatographic resolution of stereoisomeric dipeptides
R. Pätzold, H. Brückner, Dept. of Food Sciences, University
of
Giessen, Giessen, Germany
P10.
Chiral
resolution of non-proteinogenic and meteoritic Ca-dialkylated a-amino acids
R. Pätzold, S. Haasmann, H. Brückner, Dept. of Food
Sciences, University of Giessen, Giessen, Germany
P11.
Chiral
gold nanoparticles
C. Gautier, T. Bürgi, Institut de Chimie, Université de
Neuchâtel,
Neuchâtel, Switzerland
P12.
Design,
synthesis and self-assembly of chiral cleft
structures
S. Stoncius, E. Orentas, K. Warnmark, O. F. Wendt, K. Larsson, L.
Öhrström, E.
Butkus, Dept. of Organic Chemistry, Vilnius University,
Vilnius,
Lithuania & Dept. of Chemistry, Lund University, Lund & Dept. of Materials and Surface
Chemistry,
Chalmers University of Technology, Gothenburg,
Sweden
P13.
Enantioselective
HPLC separation, chiroptical properties and absolute configuration of
an
inherently chiral spiropyridine
S. Caccamese, N. Parrinello, J. A. Varela, C. Saá, M. Claps, C.
Rosini, Dip.
Scienze
Chimiche,
Universitŕ di Catania, Catania, Italy & Dep. de Quimica Organica,
Universidade de Santiago de Compostela, Santiago de Compostela, Spain
&
Dip. di Chimica, Universitŕ della Basilicata, Potenza,
Italy
P14.
Optical
isomers to highlight the stereospecific activation of the
enigmatic I1-receptor
C. Cardinaletti, A. Carrieri, F. Gentili, F.
Ghelfi, M.
Giannella, A. Piergentili, W. Quaglia, C. Vesprini, M. Pigini, Dip.
di
Scienze Chimiche, Universitŕ di Camerino, Camerino & Dip. Farmaco-Chimico,
Universitŕ di
Bari, Bari, Italy
P15.
Synthesis
and reactivity of chiral benzoquinonimes acetals
M. C. Carreńo, M. Ortega, M. Ribagorda, Dep. de Química
Orgánica,
Universidad Autónoma de Madrid, Madrid,
Spain
P16.
Facile
one-pot synthesis of BINOL and H8-BINOL-derived aryl phosphites and
their use
in palladium-catalyzed asymmetric allylation
V. Davankov, S. Lyubimov, S. Zheglov, A. Safronov, K. Gavrilov, Inst.
of Organoelement Compounds, Russian Academy of Sciences, Moscow, &
Dept. of
Chemistry, Ryazan State Pedagogic University, Ryazan,
Russia.
P17.
Enantioselective
crystallization on chiral self-assembled
monolayers
D. Dressler,
Y. Mastai, Dept. of Chemistry, Bar-Ilan University, Ramat-Gan,
Israel
P18.
Cellulases
as chiral selectors and model system for molecular
design
A. Fagerström,
M. Nilsson, U. Berg, R. Isaksson, Dept of Organic Chemistry, Lund
University, Lund, & Dept. of Chemistry and Biomedical
Sciences, University of Kalmar, Kalmar,
Sweden
P19.
Enantioselective
epoxidation of homoallylic alcohols catalyzed by the receptor-type
chiral
titanium
complexes
R.
Nishida,
H. Ito, H. Furuno, J. Inanaga, Dept. of Molecular
Chemistry, &
Inst. for Materials Chemistry and Engineering, Kyushu University,
Fukuoka, Japan
P20.
Induced
helix formation of oligophenol derivatives in
water
H.
Goto, Y.
Furusho, E. Yashima, Yashima Super-structured Helix Project,
ERATO, JST,
& Nagoya University, Nagoya,
Japan
P21.
Asymmetric
interactions in gas phase clusters: chiral recognition
processes
D.
Catone, A.
Giardini, A. Paladini, S. Piccirillo, F. Rondino, M. Satta,
M. Speranza, Dip.
di Chimica, & CNR-IMC, & Dip. di Studi di Chimica e Tecnologia
delle
Sostanze Biologicamente Attive, Universitŕ “La Sapienza”, & Dip. Scienze
e Tecnologie Chimiche, Universitŕ “Tor Vergata”, Roma,
Italy
P22.
Supramolecular
stereocontrol of biaryl configuration and translation into an
enantioselective
[1,2]-Stevens rearrangement
M.-H. Gonçalves, J. Lacour, Dept. of Organic
Chemistry, University of Geneva, Geneva, Switzerland
P23.
Towards
total synthesis of schizozygine: model synthesis of
15-hydroxystrempeliopine
T. Pilarčík, J. Hájíček, ZENTIVA VÚFB, a.s., R & D
Synthesis Group II, Prague 10, Czech Republic
P24.
Asymmetric
induction by cholestanic moiety on tropos species: synthesis and
stereochemical
characterization of bile acid-based biphenyl phosphates
A. Iuliano, S. Facchetti, G. Uccello-Barretta, Dip. di
Chimica e
Chimica Industriale, Universitŕ di Pisa, Pisa,
Italy
P25.
Photodecomposition
and chirality of aspartic acid: wavelength- and phase-dependence
Y. Izumi, T. Koketsu, S. Saijo, T. Mochida, K. Nakagawa, Graduate
School of Human Science and Cultural Studies, & Faculty of Human
Development, & Graduate School of Education, Kobe University, Kobe,
Japan
P26.
A
convenient route for the preparation of P-N and P-S ligands
M. A. Jalil, E. B. Hui, Inst. of Chemical and
Engineering Sciences, Jurong Island, Singapore
P27.
The
role of halogenides in chiral recognition by Balhimycin
Z. Jiang, R. D. Süssmuth, V. Schurig, N. W. Smith, Dept.
of
Pharmacy, King's College, London, UK & Inst. of Organic
Chemistry,
University of Tübingen, Tübingen, Germany
P28.
Click
chemistry in Cinchona alkaloids transformations - Toward new selectors
and
catalysts
K. Kacprzak, Dept. of Chemistry, A. Mickiewicz University,
Poznań, Poland
P29.
Chiral
acylphosphites and pyrophosphates - Novel ligands for asymmetric
hydrogenation
A. Korostylev, V. Tararov, A. Monsees, A. Börner, Leibniz-Institut
für Organische Katalyse an der Universität Rostock e.V., Rostock, &
Degussa
AG, Projekthaus Katalyse, Frankfurt/Main, Germany
P30.
A
new model of light powered chiral molecular motor with higher speed of
rotation: dynamics of motor rotation
T. Fujita, S. Kuwahara, N. Harada, Inst. of
Multidisciplinary
Research for Advanced Materials, Tohoku University, Sendai, Japan
P31.
Preparation
of enantiopure Wieland-Miescher ketone and derivatives by the MNP acid
method. Substituent effect on the HPLC separation
Y. Kasai, K. Shimanuki, S. Kuwahara, N. Harada, Inst. of
Multidisciplinary Research for Advanced Materials, Tohoku University,
Sendai, Japan
P32.
Triarylmethylphosphonium cations: supramolecular
stereocontrol
and exact
racemization
mechanism
B. Laleu, G.
Bernardinelli, J. Lacour, Dept. of Organic Chemistry, University of
Geneva, Geneva, Switzerland
P33.
Solution
behaviour of a new class of helical supramolecular arrays containing
lanthanides
M. Lama, O. Mamula, Inst. of Chemical Sciences and
Engineering,
Ecole Polytechnique Fédérale de Lausanne, Lausanne, Switzerland
P34.
Configurationally
stable Tröger’s base
methylates
D. A. Lenev, K. A. Lyssenko, D. G. Golovanov, R. G.
Kostyanovsky, Semenov
Inst. of Chemical Physics, & Nesmeyanov Inst. of Organoelement
Compounds, Russian Academy of Sciences, Moscow, Russia
P35.
Practice and theory of GC separation of enantiomers on
mixed chiral stationary phases
P.A. Levkin, V. Schurig, Inst. of Organic Chemistry,
University of Tübingen, Tübingen, Germany
P36.
Solid-state
ESR differentiation between enantiomers vs. racemates
P. A. Levkin, A. I. Kokorin, V. Schurig, R. G. Kostyanovsky, Inst.
of
Organic Chemistry, University of Tübingen, Tübingen, Germany & N.
N.
Semenov Inst.itute of Chemical Physics, Russian Academy of Sciences,
Moscow, Russia
P37.
Eluent
versatility for chiral separations with Eurocel 01
S. Marten, H. Knauer, Wissenschaftliche Gerätebau Dr. Ing. Herbert Knauer
GmbH,
Application and Column Dept., Berlin, Germany
P38.
Chiral
recognition on a supramolecular level in optical resolutions
K. Marthi, D. Kozma, G. Pokol, F. Faigl, E. Fogassy, Research
Group
of Technical Analytical Chemistry, & Inst. for Organic
Chemistry, &
Inst. of General and Analytical Chemistry, Hungarian Academy of
Sciences –
Budapest University of Technology and Economics, Budapest,
Hungary
P39.
Chiral
polymers for enantioselective crystallization of amino
acids
T. Menahem,
Y. Mastai, Dept. of Chemistry, Bar-Ilan University, Ramat-Gan,
Israel
P40.
Temperature-driven
helix-sense inversion of a helical poly(phenylacetylene) derivative and
memory
of the macromolecular helicity
T. Miyagawa, A. Furuko, K. Maeda, E. Yashima, Yashima
Super-structured Helix Project, ERATO, JST, & Dept. of Molecular
Design and
Engineering, Nagoya University, Nagoya, Japan
P41.
Enantioresolution
of organic substances by cholic and deoxycholic acids as well as their
epimers
K. Matsui, K. Aburaya, N. Tohnai, M. Miyata, Dept. of
Material and
Life Science, Osaka University, Osaka,
Japan
P42.
Optical
resolution of amino acids via the Carica papaya lipase-catalysed
transesterification
T. Miyazawa, K. Onishi, S.-W. Tsai, Dept. of
Chemistry, Konan University, Kobe, Japan, & Dept. of Chemical
Engineering, National Chen Kung University, Tainan, Taiwan
P43.
Cu-salicylaldiimine
complexes on polysiloxane: new heterogeneous catalysts for
stereoselective
synthesis of (+)-chrysanthemic acid
L. Moroni, S. Carloni, G. Tanzi, R. Maggi, G. Sartori, V.
Borzatta, ENDURA
S.p.A., Ravenna, & Dip. di Chimica Organica e Industriale,
Universitŕ di
Parma, Parma, Italy
P44.
Molecular
design of light–driven chiral “supramolecular”
scissors
S. Nara, T. Muraoka, K. Kinbara, T. Aida, Dept. of Chemistry
and
Biotechnology, University of Tokyo, Tokyo, & PRESTO, Japan Science
and
Technology Agency (JST), Japan
P45.
Heptakis(6-O-(N-acetylyl-l-valine-tert-butylamide)-2,3-di-O-methyl)-b-cyclodextrin:
a promising chiral solvating agent for NMR determinations of
enantiomeric
compositions
G.
Uccello-Barretta, S. Nazzi, P. Levkin, V. Schurig, Dip. di
Chimica e
Chimica Industriale, Universitŕ di Pisa, Pisa, Italy & Inst. für
Organische
Chemie, Universität Tübingen, Tübingen, Germany
P46.
Synthesis
and resolution of the first enantiopure bowl-shaped
molecule
P. Mobian, E. R. Francotte, C. Nicolas, J. Lacour, Dept. of
Organic
Chemistry,University of Geneva, Geneva, & Novartis Institutes for
Biomedical Research, Basel, Switzerland
P47.
Electronic
and vibrational circular dichroism study of non covalent interactions
of a
novel brucine porphyrins with DNA
J. Nový, V. Král, M. Urbanová, Dept. of Analytical
Chemistry, &
Dept. of Physics and Measurements, Inst. of Chemical Technology,
Prague, Czech Republic
P48.
Vibrational and electronic circular dichroism study of
guanine-rich oligonucleotide and its interactions with
5,10,15,20–tetrakis(1-methyl-pyridinium-4-yl) porphyrin
J. Nový, V. Král, M. Urbanová, Dept. of Analytical
Chemistry, &
Dept. of Physics and Measurements, Inst. of Chemical Technology,
Prague, Czech Republic
P49.
Vibrational
and electronic circular dichroism study of non covalent interactions of
cationic porphyrins with synthetic
oligonucleotides
J. Nový, M. Urbanová, Dept. of Analytical Chemistry, &
Dept. of
Physics and Measurements, Inst. of Chemical Technology, Prague, Czech
Republic
P50.
Vibrational
and electronic circular dichroism as a tool for the studies of the
DNA–porphyrin interaction
J.
Nový, M. Urbanová, Dept. of
Analytical Chemistry, & Dept. of Physics and Measurements, Inst. of
Chemical Technology, Prague, Czech
Republic
P51.
Asymmetric
reactions via radical intermediates: solid state-specific, asymmetric
photoisomerization and dioxygenation reaction of w-substituted
alkyl cobaloxime complexes
Y. Ohgo, Y.
Seki, K. Ikeda, K. K. Orisaku, Y. Arai, Niigata University
of
Pharmacy and Applied Life Sciences, Niigata, Japan
P52.
Development
and synthesis of bicyclic ligands for asymmetric catalysis
C. Olsson, A. Friberg, T. Frejd, Dept. of
Organic
Chemistry, Lund University, Lund, Sweden
P53.
Ring
opening metathesis polymerization of optically active N-substituted
tetrahydrophthalimide with ruthenium
catalyst
K. Onimura,
S. Kuroiwa, Y. Isobe, T. Oishi, Dept. of Applied Chemistry &
Chemical
Engineering, Yamaguchi University, Yamaguchi, Japan
P54.
Copper-bis(oxazoline)
complexes as enantioselective catalysts for the preparation of
optically active
nitroalcohols
C. Oro, R. Maggi, G. Sartori, O. Vecchi, Dip. di Chimica
Organica e
Industriale, Universitŕ di Parma, Parma,
Italy
P55.
Metal
cation-induced helix inversion for poly(phenylacetylene) bearing
polycarbohydrate
ionophore as graft chain
I. Otsuka, R. Sakai, T. Satoh, R. Kakuchi, H. Kaga, T. Kakuchi, Div.
of Biotechnology and Macromolecular Chemistry, Hokkaido University,
& Div.
of Innovative Research, Natl. Institute of Advanced Industrial Science
and
Technology, Sapporo, Japan
P56.
Chiral
ferrocenyl derivatives containing a biphenyl unit: atropisomeric
stability and
stereoselective
synthesis
A. Patti, S. Pedotti, Istituto di Chimica Biomolecolare del
CNR –
Sez. di Catania, Via del Santuario 110, I-95028 Valverde (CT),
Italy
P57.
Chiral
epimeric carboxycylopentylglycines from norbornane derivatives:
reaction
conditions and ring strain effect on stereochemical control of amino
acid
centers
M. L. Gelmi, S. Pellegrino, Ist. di Chimica Organica “A.
Marchesini”, Milano,
Italy
P58.
Structural
investigation of BINOL/titanium(IV) asymmetric catalysts by means of CD
and NMR
spectroscopy in solution
G. Pescitelli, L. Di Bari, P. Salvadori, Dept. of Chemistry,
University of Pisa, Pisa, Italy
P59.
High-performance
liquid chromatographic enantioseparation of bicalutamide and its
related
compounds
A.
Péter, R. Török, Á. Bor, F. Lukács,
G. Orosz, D. Armstrong, Dept. of Inorganic and Analytical
Chemistry, University of Szeged, Szeged, & CF Pharma Ltd, Budapest,
Hungary & Dept. of Chemistry, Iowa State University, Ames, IA,
USA
P60.
p-Quinols and p-quinamines:
an open door to structural diversity
M. C. Carreńo, M. Ribagorda, M. J. Sanz-Cuesta, Dep. de Química
Orgánica,
Universidad Autónoma de Madrid, Madrid,
Spain
P61.
Helically organized crown ether array parallel to the
helix axis of polyisocyanate
R. Sakai, I. Otsuka, T. Satoh, R. Kakuchi, H. Kaga, T.
Kakuchi, Div.
of Biotechnology and Macromolecular
Chemistry, Hokkaido University, & Div. of Innovative Research,
Creative
Research Initiative “Sousei”, & Natl. Inst. of Advanced Industrial
Science
and Technology, Sapporo,
Japan
P62.
Bicyclo[3.2.0]hept-3-en-6-ones
as a source of new chiral backbones for asymmetric catalysts
G. Rosini, E. Marotta, P. Righi, N. Scardovi, Dip. di
Chimica Organica
“A. Mangini”, Universitŕ di Bologna, Bologna,
Italy
P63.
Macrocyclic
uranyl salophen complexes: a new class of inherently chiral
receptors and catalysts
A. Dalla Cort, L. Mandolini, C. Pasquini, L. Schiaffino, Dip.
di
Chimica, Universitŕ “La Sapienza and IMC-CNR, Sezione Meccanismi, Roma,
Italy
P64.
Direct
irradiation of circularly polarized light and asymmetric autocatalysis
as a
possible origin of homochirality
T.
Kawasaki,
M. Sato, S. Ishiguro, T. Saito, Y. Morishita, I. Sato, H. Nishino, Y.
Inoue, K.
Soai, Dept. of Applied Chemistry, Tokyo University of Science,
Tokyo,
& Entropy Control Project, ICORP, Osaka,
Japan
P65.
Asymmetric autocatalysis in the presence of achiral
silica gel without adding chiral substance
K. Suzuki, M.
Shimizu, K. Ishikawa, T. Kawasaki, K. Soai, Dept. of Applied
Chemistry, Tokyo University of Science, Tokyo,
Japan
P66.
Chiral
discrimination of 2,3-bis-fluoren-9-ylidenesuccinic acid by inclusion
crystallization with achiral guest
K. Tanaka, S. Wada, M. R. Caira, Dept. of Applied Chemistry, Kansai
University, Osaka, Japan, & Dept. of Chemistry, University of Cape
Town,
Rondebosch, South Africa
P67.
Construction
of artificial double helices using amidinium-carboxylate salt bridge
formation
Y. Tanaka, H. Katagiri, Y. Furusho, E. Yashima, Japan
Science &
Technology Agency, ERATO Yashima Super-Structured Helix Project,
Nagoya, Japan
P68.
Structural
analysis of filamentous bacteriophages via their liquid crystal
properties
S. Tomar, M. M. Green, L. A. Day, Othmer Dept. of Chemical
and
Biological Sciences and Engineering, Polytechnic University,
Brooklyn, NY, & The Public Health Research Institute, Newark, NJ,
USA
P69.
Enantioselective
nitroaldol (Henry) reaction catalyzed by chiral complexes of lanthanide
(III)
triflates
F. Tur, J. M. Saá, J. F. González, M. Vega, Dep. de Química,
Universitat de les Illes Balears, Palma de Mallorca,
Spain
P70.
Synthesis
and resolution of the first non racemic
diquats
J. Vachon, G.
Bernardinelli, J. Lacour, Dept. of Organic Chemistry, University of
Geneva, Geneva,
Switzerland
P71.
HPLC
resolution of chiral [4]heterohelicenium dyes on chiral stationary
phases
B. Laleu, P. Mobian, J. Lacour, C. Villani, Dept. of
Organic
Chemistry, University of Geneva, Geneva, Switzerland, & Dip. di
Studi di
Chimica e Tecnologia delle Sostanze Biologicamente Attive, Universitŕ
"La Sapienza", Roma, Italy
P72.
Substrate
controlled tropoisomerization of ligands for asymmetric allylic
substitution
R. Zalubovskis, R. Stranne, J.-L. Vasse, C. Moberg, Dept. of
Chemistry, Royal Institute of Technology, Teknikringen,
Sweden
P73.
Enantiomer
separation in immunoaffinity LC-MS
O. Hofstetter, J. M. Zeleke, G. B. Smith, H. Hofstetter, Dept.
of
Chemistry and Biochemistry, Northern Illinois University, DeKalb, IL,
USA
P74.
Stereoselective
antibodies to free a-hydroxy
acids
O. Hofstetter, T. K. Zeleke, J. M. Zeleke, H. Hofstetter, Dept.
of
Chemistry and Biochemistry, Northern Illinois University, DeKalb, IL,
USA
Tuesday,
13 Sept.,
Afternoon
14.00-15.00
SESSION B
Faculty of
Engineering
P75.
Enantioresolution
of various alcohols by bile
amides
K. Aburaya, N. Tohnai, M. Miyata, Dept. of Material and Life
Science, Osaka University, Osaka,
Japan
P76.
Gas
chromatographic-mass spectrometric search for d-amino
acids in vertebrates
R. Pätzold, H. Brückner, Dept. of Food Sciences, University
of
Giessen, Giessen, Germany
P77.
Formation
of D-amino acids in the course of the Maillard
reaction
R.
Pätzold,
H. Brückner, Dept. of Food Sciences, University of Giessen,
Giessen,
Germany
P78.
Vibrational
Circular Dichroism in the Near-Infrared (NIR-VCD): current
measurements, data
interpretation and future applications
S. Abbate, G. Longhi, E. Castiglioni, Dip. di Scienze
Biomediche e
Biotecnologie, Universitŕ di Brescia, Brescia,
Italy
P79.
“Garage
accessories” for commercial CD spectrometers
P.
Albertini, E. Castiglioni, JASCO Europe srl, Cremella,
Italy &
JASCO Corporation, Tokyo, Japan
P80.
Analysis
of the conformations of (R)-(-)-a-phenylethylamine
in the free and protein bound states by
Vibrational Spectroscopy (IR and VCD)
B. K. Chavali, K. Krishnamurthy, J. L. Dage, Discovery
Chemistry
Research and Technologies, Lilly Research Laboratories, Indianapolis,
IN,
USA
P81.
Optimization
of binding strategies in the preparation of macrocyclic glycopeptide
antibiotic
chiral stationary phases
A. Ciogli, I. D’Acquarica, F. Gasparrini, D.
Misiti, C.
Villani, Dip. di Studi di Chimica e Tecnologia delle Sostanze
Biologicamente
Attive, Universitŕ “La Sapienza”, Roma, Italy
P82.
Enantiomers
of
novel anti-inflammatory pyrrole derivatives: analytical and
semipreparative
HPLC separation, and chiroptical properties
M. Biava, R. Cirilli, R. Ferretti, F. La Torre, G. Poce, G. C.
Porretta, C. Villani, Dip. di Studi di Chimica e Tecnologia delle
Sostanze Biologicamente Attive, Universitŕ “La Sapienza”, &
Dip. del Farmaco, Istituto Superiore di Sanitŕ, Roma,
Italy.
P83.
Direct
HPLC enantioseparation of new substituted
1-thiocarbamoyl-3,5-diaryl-4,5-dihydro-(1H)-pyrazoles on Chiralcel
OJ-RH and
Chiralpak IA chiral stationary phase
O. Befani, A. Bolasco, P. Chimenti, R. Cirilli, R. Ferretti, F.
La Torre, E. Maccioni, D. Secci, A. Simonelli, Dip. di Scienze
Biochimiche “A. Rossi
Fanelli”, Universitŕ “La Sapienza”, & Centro di Biologia Molecolare
del
CNR, & Dip. di Studi di Chimica e Tecnologia delle Sostanze
Biologicamente
Attive, Universitŕ “La Sapienza”, & Dip. del Farmaco, Istituto
Superiore di
Sanitŕ, Roma, & Dip Farmaco Chimico Tecnologico, Universitŕ degli
Studi,
Cagliari, Italy
P84.
Ionic
GC-MS detection of chiral markers in Cocoa seeds of
different
quality and geographic origin
A. Caligiani, M. Cirlini, G. Palla, R. Ravaglia, M. Arlorio, Dip.
di
Chimica Organica e Industriale, Universitŕ degli Studi, Parma, &
STREGLIO
Maestri del Cioccolato S.p.A., None (TO), & DiSCAFF, Novara,
Italy
P85.
Production
and
characterization of sol-gel coatings in fused-silica capillaries for
chiral
separation by capillary electrophoresis
F. Bianchi, M. Careri, C. Corradini, A. Mangia, G. Predieri, A.
Stercoli, Dip. di Chimica Generale ed Inorganica, Chimica
Analitica, Chimica
Fisica, Universitŕ di Parma, Parma,
Italy
P86.
The
DACH-DNB
chiral stationary phase as a tool for ultra-fast enantioselective HPLC:
a step
towards enantioselective UPLC
A. Ciogli, I.
D’Acquarica, F. Gasparrini, R. Rompietti, C. Villani, F. Mannerino,
T.
Szczerba, Dip. di Studi di Chimica e Tecnologia delle Sostanze
Biologicamente Attive, Universitŕ “La Sapienza”, Roma, Italy &
Regis Technologies, Inc., Morton Grove, IL,
USA
P87.
Determination of activation barriers for hindered
rotation and absolute conformations in axially chiral heterocyclic
compounds
O. Demir Ordu, E. M. Yilmaz, I. Dogan, Dept. of Chemistry,
Boğaziçi University, İstanbul, Turkey.
P88.
Epimerization
study of dihydroartemisinin (DHA) by dynamic HPLC and spectroscopic
techniques
A. Alfarone, D. Carnevale, I. D’Acquarica, M. Di Mattia, F.
Gasparrini,
F. Giorgi, S. Lalli, M. Pierini, C. Masaracchia, M. Quaglia, Analytical
Chemistry Dept., R & D, Sigma-Tau S.p.A., Pomezia (RM), & Dip.
di Studi
di Chimica e Tecnologia delle Sostanze Biologicamente Attive,
Universitŕ “La Sapienza”, Roma, Italy
P89.
Determination
of energy barriers to rotation in 2-arylimino-3-aryl-thiazolidine-4-one
derivatives
S.
Erol,
I. Dogan, Dept. of Chemistry, Boğaziçi University, İstanbul,
Turkey.
P90.
Chiral
recognition mechanism of 1,4-dihydropyridines on amylose
tris(3,5-dimethylphenyl carbamate) chiral stationary phase
V. Drušković, M. Litvic, A. Bartolinčić, A. Šporec, V.
Vinković, Belupo Pharmaceuticals and Cosmetics Ltd., & Ruđer
Bošković Institute, Zagreb, Croatia
P91.
Chiral
recognition mechanism of b-amino
alcohols on amylose tris(3,5-dimethylphenyl carbamate) chiral
stationary phase
V. Drušković,
A. Šporec, I. Cepanec, A. Bartolinčić, V. Vinković, Belupo
Pharmaceuticals and Cosmetics Ltd., & Ruđer Bošković Institute,
Zagreb, Croatia
P92.
Determination
of absolute configuration of molecules of pharmaceutical interest by
VCD
spectroscopy
L.
Nafie, T.
Freedman, X. Cao, R. Dukor, Dept. of Chemistry, Syracuse
University, Syracuse, NY, & BioTools, Inc., Wauconda, IL, USA
P93.
Monitoring
the epimerization of 2,2-dimethyl-1,3-dioxolane-4-methanol using
near-infrared
Vibrational Circular Dichroism
Spectroscopy
L.
Nafie, C.
Guo, X. Cao, T. Freedman, R. Dukor, Dept. of Chemistry,
Syracuse
University, Syracuse, NY, & BioTools, Inc., Wauconda, IL,
USA
P94.
Application
of a new enantiopure chiral crown ether based chiral stationary phase
in
enantioseparation of racemic primary organic ammonium
salts
V. Farkas, T. Tóth, P. Huszthy, M. Hollósi, G. Orosz, Dept.
of
Organic Chemistry, Eötvös Loránd University, & Inst. for Organic
Chemistry, Budapest University of Technology and Economics, &
Reanal Fine Chemicals
Co., Budapest, Hungary
P95.
Investigations
into the chiral separation of amino acid derivatives using chiral hosts
based
on cinchona alkaloids
J. Floure, J. G. de Vries, A. J. Hallet, G. Kwant, L. Duchateau,
DSM
Research, DSM Fine Chemicals, Geleen, The
Netherlands.
P96.
Chiral
terpene
flavours of blood orange and lemon juice: effect of high-pressure
treatment and
ohmic heating
G. Galaverna, G. Di Silvestro, A. Dossena, R. Marchelli, Dip. di Chimica Organica e
Industriale, Universitŕ
di Parma, Parma, & Parmalat S.p.A., Centro Ricerche, Castellaro di
Sala
Baganza (PR), Italy.
P97.
Preparation
and evaluation of the enantiomer separation characteristics of novel
diastereomeric bis-cinchona phthalazine type receptors
E. Gavioli, N. M. Maier, W. Lindner, Dept. of Analytical
Chemistry
and Food Chemistry, University of Vienna, Vienna,
Austria
P98.
Enantioselective
GC and HPLC analysis of cyclopropane
derivatives
A. Ghanem, Biological
and Medical Research Dept., King Faisal Specialist Hospital and
Research Center, Riyadh, Saudi Arabia
P99.
On
the solvent versatility in immobilized amylose
tris-(3,5-dimethylphenylcarbamate)
chiral stationary phase in High-Performance Liquid Chromatography:
application
to the asymmetric cyclopropanation of olefins
A. Ghanem, H. Y. Aboul-Enein, Centre for Clinical Research,
King
Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia
P100.
Chiral
separation of enantiomers of some agrochemical toxins by High-
Performance
Liquid Chromatography on a vancomycin crystalline degradated
products-chiral
stationary phase
S.
Chalavi, A.
Ghassempour, K. Tabar-Heydar, M. M. Mojtahedi, H.Y. Aboul-Enein, Dept.
of Chemistry, & Medicinal Plants and Drugs Res. Inst., Shahid
Beheshti
University, & Chemistry and Chemical Engineering Research Center,
Tehran,
Iran & Centre for Clinical Research, King Faisal Specialist
Hospital and Research
Center, Riyadh, Saudi Arabia
P101.
A
selective 31P NMR spectroscopic method for study of
Trichlorfon
Z. Talebpour, A. Ghassempour, M. Zandehzaban, Dept. of
Chemistry, Alzahra University, & Medicinal Plants and Drugs
Research Inst., Shahid Beheshti University, Tehran, Iran
P102.
Speed
up chiral column screening with parallel HPLC
H. Gumm, A. Bredebusch, Sepiatec GmbH, Berlin,
Germany
P103.
Enantioselective
membranes: preparation and characterization of chiral polysulfones
B. Gutiérrez,
C. Minguillón, Institut de Recerca Biomčdica, Parc Científic de
Barcelona
& Laboratori de Química Farmacčutica, University of Barcelona,
Barcelona,
Spain
P104.
Diffuse
Reflectance CD (DRCD) spectrophotometer: development and application
T. Harada, R. Kuroda, ERATO-SORST Kuroda
Chiromorphology
Team, Japan Science and Technology Agency, & Graduate School of
Arts and
Sciences, University of Tokyo, Tokyo, Japan
P105.
In-situ polarimetric
monitoring of a
one-pot catalysed synthesis of enantiopure secondary alcohols
E. A. Haywood,
D. M. Goodall, E. T. Bergström, G. D. Jonas, Dept. of Chemistry,
The
University of York, Heslington, & GlaxoSmithKline
Pharmaceuticals,
Computational, Analytical and Structural Science, Harlow,
UK
P106.
Enantioseparation
of aromatic amino acids and aralkylammonium salts by HPLC using a
chiral crown
ether-based sorbent
M. Hollósi, V. Farkas, T. Tóth, P.Huszthy, I. Laczkó, Dept.
of
Organic Chemistry, Eötvös Loránd University, & Inst. for Organic
Chemistry,
Budapest University of Technology and Economics, Budapest, &
Biological
Research Center, Hungarian Academy of Sciences, Szeged, Hungary
P107.
Liquid
chromatographic resolution of secondary amino alcohols on a HPLC chiral
stationary phase based on chiral crown ether
M. H. Hyun, Y. J. Park, Dept. of Chemistry and Chemistry
Inst. for
Functional Materials, Pusan National University, Busan, Korea
P108.
Conformational
investigations of naturally occurring, pharmaceutically relevant,
chiral g‑butyrolactones
and derived
molecules: a VCD analysis
G. Thomas, S. H. Varghese, B. Chavali, I. Ibnusaud, School
of
Chemical Sciences, Mahatma Gandhi University, Kerala, India &
Eli Lilly
and Company, Indianapolis, IN, USA
P109.
High-performance
liquid chromatographic enantioseparation of imino acids on a chiral
ligand-exchange
column
I. Ilisz, A.
Péter, D. Tourwé, D. Armstrong, Dept. of Inorganic and Analytical
Chemistry,
University of Szeged, Szeged, Hungary & Eenheid Organische Chemie,
Vrije
Universiteit Brussels, Brussels, Belgium & Dept. of Chemistry, Iowa
State
University, Ames, IA, USA
P110.
Peptide
nucleic acids as templates to study cooperative responses to chirality
in
helical sense choice
V. Jain, A. Faccini, T. Tedeschi, R. Corradini, M. M.
Green, Othmer
Dept. of Chemical and Biological Sciences and Engineering, Polytechnic
University, Brooklyn, NY, USA & Dip. di Chimica Organica e
Industriale,
Universitŕ di Parma, Parma, Italy
P111.
Chiral
separation of pyrethroic acids with various capillary chromatographic
techniques using cyclodextrin selectors
Z. Juvancz, R. Iványi, VITUKI Plc., & Cyclolab R&D.
Ltd., Budapest, Hungary
P112.
Monoimides
of DACH - Useful chiral derivatizating reagents for the determination
of
enantiomeric excess using NMR spectroscopy
M. Kaik, J. Gawroński, Dept. of Chemistry, A. Mickiewicz
University, Poznań, Poland
P113.
Preparation
of novel β-cyclodextrin based inclusion complex/molecular
necklace and
evaluation as optical chiral sensor
K. P. Lee, A. I. Gopalan, J. H. Kim, M. S. Kim, J. S. Kang, Dept.
of
Chemistry, Kyungpook National University, & Nanocenter for
Practical
Applications, Daegu, South Korea & Dept. of Industrial Chemistry,
Alagappa
University, Karaikudi, India
P114.
Synthesis
of molecularly imprinted organic-inorganic hybrid polymers for
enantioselective
separation of naproxen
J. S. Kang, K. P. Lee, A. I. Gopalan, M. S. Lee, Dept. of
Chemistry,
Kyungpook National University, & Nanocenter for Practical
Applications,
Daegu, South Korea & Dept. of Industrial Chemistry, Alagappa
University,
Karaikudi, India
P115.
Synthesis and spectroscopic evaluation of chiral
selectors in chiral stationary phases
G. Landek, D. Kontrec, V. Vinković, Ruđer Bošković
Institute, Zagreb, Croatia
P116.
Geometrical
and algebraic approach to central molecular chirality: a chirality
index and an
Aufbau description of tetrahedral molecules
S. Capozziello, A. Lattanzi, Dip. di Scienze Fisiche &
INFN (Sez.
di Napoli), Universitŕ di Napoli “Federico II”, Napoli, & Dip. di
Chimica,
Universitŕ di Salerno, Baronissi (SA),
Italy
P117.
Liquid
chromatographic enantiomer resolution of N-fluorenyl methoxycarbonyl a-amino acids and
their ester derivatives
on polysaccharide-derived chiral stationary
phases
W. Lee, Y. H.
Li, College of Pharmacy, Chosun University, Kwangju, South
Korea
P118.
Chiral
discrimination studies of (+)-(18-crown-6)-2,3,11,12-tetracarboxylic
acid by
High-Performance Liquid Chromatography and NMR spectroscopy
W. Lee, W.-T. Lee, College of Pharmacy, Chosun
University, Kwangju, & Dept. of Biochemistry, Yonsei University,
Seoul, South Korea
P119.
Determination
of surface chirality by near-field scanning optical
microscopy
Y. Mastai, A. Landow, D. H. Derssler, A. Zaban, Dept. of
Chemistry,
Bar-Ilan University, Ramat-Gan, Israel
P120.
Enantioselective
detection of DOPA by using gold electrode modified with cysteine and
homocysteine monolayers by electrochemical
method
M. Matsunaga, T. Nakanishi, M. Nagasaka, C. Tatsumi, T. Asahi,
T. Osaka,
Dept. of Applied Chemistry, & Institute for Biomedical
Engineering, Waseda University, Tokyo, Japan
P121.
Application
of chiral technology in a pharmaceutical company. Solution
studies of key
asymmetric intermediates using a combination of spectroscopic
techniques
O. McConnell, Y. He, Wyeth Research, Discovery
Analytical
Chemistry, Collegeville, PA, USA
P122.
Extension
of vibrational circular dichroism into the near-infrared region beyond
10,000 cm-1
L. Nafie, C. Guo, X. Cao,
Dept. of
Chemistry, Syracuse University, Syracuse, NY,
USA
P123.
Chiro-optical
study of nano-structured materials using the G-HAUP
N. Nakamura, M. Tanaka, I. Kagomiya, T. Asahi, T. Osaka, K.
Kuroda, M.
Ogawa, Waseda University, Graduate School of Science and
Engineering, Tokyo,
& National Inst. of Advanced Industrial Science and Technology,
Tsukuba
Ibaraki, & Institute for Biomedical Engineering, & Faculty of
Education
and Integrated Arts and Sciences, Waseda University, Tokyo,
Japan
P124.
Dynamic
ligand-exchange chiral stationary phase from S-benzyl-(R)-cysteine
B. Natalini, R. Sardella, R. Pellicciari, Dip. di Chimica e
Tecnologia del Farmaco, Universitŕ di Perugia, Perugia, Italy
P125.
Enantioresolution
of acyclic diol derivatives and determination of their absolute
configurations
by the MaNP acid method
K. Noro, S. Kuwahara, M. Watanabe, N. Harada, Inst. of
Multidisciplinary Research for Advanced Materials, Tohoku University,
Sendai, Japan
P126.
Comparison
of the resolution of chiral compounds on coated and immobilized
polysaccharide
chiral stationary phases
K. Öhlén, L. Thunberg, S. Andersson, AstraZeneca R
& D Mölndal, Mölndal, Sweden
P127.
Asymmetric
anionic polymerization of N-maleoyl-l-leucine
derivatives with chiral ligand/organometal complexes and chiral
recognition
abilities of their polymers
T. Oishi, K. Onimura, Y. Isobe, Dept. of Applied Chemistry
&
Chemical Engineering, Yamaguchi University, Yamaguchi,
Japan
P128.
Optimization
of cellulose 3,5-dimethylphenylcarbamate as chiral selector in the
separation
of enantiomers by pH-zone refining centrifugal partition
chromatography
E. Pérez, C.
Minguillón, Inst. de Recerca Biomčdica, Parc Científic de
Barcelona, &
Lab. de Química Farmacčutica, University of Barcelona Barcelona,
Spain
P129.
Absolute configuration and predominant conformations of t-butylphenyl
phosphinic amide
A. G. Petrovic,
P. L. Polavarapu, J. Drabowicz, A. Łopusinski, M. Mikołajczyk, A.
Filipczak, M. W. Wieczorek, Dept. of Chemistry, Vanderbilt
University,
Nashville, TN, USA & Center for Molecular and Macromolecular
Studies,
Polish Academy of Sciences, & Inst. of Food Chemistry, Technical
University
of Łódż, Łódż, & Dept. of Chemistry and Environmental
Protection, Jan Długosz University of Częstochowa, Częstochowa,
Poland
P130.
Enantiopure
sulfinyl azobenzenes as chiroptical switches
M. C. Carreńo, I. García, M. Ribagorda, E. Merino, S. Pieraccini,
G. P.
Spada, Dep. de Química Orgánica Universidad Autónoma de Madrid,
Madrid,
Spain & Dip. di Chimica Organica “A. Mangini”, Universitŕ di
Bologna,
Bologna, Italy
P131.
A
new
extension of the dynamic chromatographic methodology to the kinetic
study of
multiple equilibria
I.
D’Acquarica, F.
Gasparrini, D. Misiti, M. Pierini, C. Villani, Dip. di
Studi di
Chimica e Tecnologia delle Sostanze Biologicamente Attive, Universitŕ
“La Sapienza”, Roma, Italy
P132.
Resolution
of
N,N-dialkyl-3-aryl-3-aryloxyamines
L. Ridvan, P. Hrubý, H. Petříčková, Zentiva, Praha, Czech
Republic
P133.
Hybrid
polyamide HPLC chiral stationary phases prepared by surface-initiated
photopolymerization
L. Caglioti, F. Gasparrini, R. Rompietti, D. Misiti, C.
Villani, Dip.
di Studi di Chimica e Tecnologia delle Sostanze Biologicamente Attive,
Universitŕ “La Sapienza”, Roma, Italy
P134.
31P NMR
determination of the
enantiomeric composition of N-protected aminophosphonates employing O-tert-butylcarbamoyl-quinine
and quinidine as chiral agent
E. Rudzińska,
Ł. Berlicki, A.Mucha, M. Lämerhofer, W. Lindner, P.Kafarski, Dept.
of
Bioorganic Chemistry, Wrocław University of Technology, Wrocław,
Poland & Inst. of Analytical Chemistry, University of Vienna,
Vienna,
Austria
P135.
Poly-(4R)-hydroxy-l-proline derivatives.
Synthesis,
characterization and suitability as chiral selectors for HPLC
R. Sancho, C. Minguillón, Institut de Recerca Biomčdica,
Parc
Científic de Barcelona & Lab. de Química Farmacčutica, University
of
Barcelona, Barcelona,
Spain
P136.
A
new unconventional method based on circular dichroism to detect peanut
and
hazelnut DNA in food by means of a PNA probe and a cyanine
dye
E. Scaravelli,
S. Sforza, T. Tedeschi, R. Corradini, R. Marchelli, Dip. di Chimica
Organica
e Industriale, Universitŕ di Parma, Parma, Italy
P137.
Optical
resolution of substituted 1-arylethylamines by its acidic derivatives
J. Schindler, J. Bálint, E. Fogassy, Research Group for
Organic
Chemical Technology, Hungarian Academy of Sciences, Budapest,
Hungary
P138.
Enantiomeric
excess determination of chiral carboxylic acids using the
enantiomer-labelled
host method by ESI mass
spectrometry
Y. Takai, K. Iguchi, M. Shizuma, H. Yamada, R. Arakawa, M.
Sawada, The
Inst. of Scientific and Industrial Research, Osaka University,
& Dept. of
Applied Chemistry, Kansai University, & Osaka Municipal Technical
Research
Institute, Osaka,
Japan
P139.
Chiral
discrimination of 3-O-substituted cyclofructans toward amino
acid
derivatives in FAB mass spectrometry
M. Shizuma, H. Adachi, M. Junge, W. A. König, Osaka
Municipal
Technical Research Institute, Osaka, Japan & Dept. of Chemistry,
Universität Hamburg, Hamburg, Germany & Faculty of Science, Osaka
University, Osaka,
Japan
P140.
Density
functional theory calculations of the optical rotations and Circular
Dichroism
spectra of helicenes
D. M. McCann, P. J. Stephens, Dept. of Chemistry,
University
of Southern California, Los Angeles, CA, USA
P141.
The
determination of absolute configuration using density functional theory
calculations of specific rotation
P. J. Stephens, D.
M. McCann, F. J. Devlin, J. R. Cheeseman, M. J. Frisch, Dept. of
Chemistry,
University of Southern California, Los Angeles, CA 90089-0482, &
Gaussian
Inc., Wallingford, Connecticut, USA
P142.
Determination
of molecular structure in solution using Vibrational Circular Dichroism
spectroscopy: the supramolecular tetramer of S 2,2'
dimethyl-biphenyl-6,6'-dicarboxylic acid
M. Urbanová, V. Setnička, F. J. Devlin, P. J. Stephens, Dept.
of
Physics and Measurements & Dept of Analytical Chemistry, Inst. of
Chemical
Technology, Prague, Czech Republic & Dept. of Chemistry, University
of
Southern California, Los Angeles, CA,
USA
P143.
The
CFTA method using NMR: a very reliable, convenient procedure for
assignment of
absolute stereochemistry of chiral secondary alcohols
Y. Takeuchi, H. Fujisawa, T. Fujiwara, K. Omata, K. Kabuto, Fac.
Pharmaceutical Sci., Toyama Med. Pharm. University, Sugitani Toyama,
&
Dept. Chemistry, Tohoku University, Aramaki Sendai, Japan
P144.
Quantum
mechanical modelling of self-reproducible living PNA chip immersed in
the lipid
bilayer vesicle controlled by quantum computing logic
gates
A. Tamulis, V. Tamulis, J. Tamuliene, Inst. of Theoretical
Physics
and Technology, Vilnius University, Vilnius,
Lithuania
P145.
Detection
of
the R553X single point mutation related to cystic fibrosis in capillary
electrophoresis by a “Chiral Box” d-lysine-peptide
nucleic acid probe
T. Tedeschi, M. Chiari, G. Galaverna, S. Sforza, M. Cretich, R.
Corradini, R. Marchelli, Dip. di Chimica Organica e Industriale,
Universitŕ di
Parma, Parma, & Ist. di Chimica del Riconoscimento Molecolare,
C.N.R.,
Milano
Italy
P146.
Teicoplanin
based chiral stationary phases for HPLC in the frame of LFER
K. Kalíková, J. Lokajová, E. Tesařová, Dept. of
Physical
and Macromolecular Chemistry, Charles University, Prague, Czech
Republic
P147.
Resolution
of secondary alcohols by lipase catalyzed hydrolysis. Chiral separation of
2-tetralol
derivatives
D. Ubiali, M.
Filice, P.
Moro, G. Speranza, P. Cairoli, T. Szczerba, M. Terrenia, Dip. di
Chimica
Farmaceutica, Universitŕ di Pavia, Pavia, & Dip. di Chimica
Organica e
Industriale, Universitŕ di Milano, Milano, Italy & Regis®
Technologies Inc., Morton Grove, IL,
USA
P148.
Preparative
enantiomer separation of structurally diverse arylalkyl-carbinols on
ULMO, a p‑donor-acceptor
type chiral
stationary phase
N. M. Maier, G. Uray, E. Gavioli, W. Lindner, Dept.
of
Analytical Chemistry and Food Chemistry, University of Vienna, Vienna,
&
Dept. of Chemistry, Karl-Franzens University, Graz,
Austria
P149.
Reversal
of elution order with immobilization of the chiral
selector
N. Vanthuyne, F. Andreoli, S. Fernandez, C. Roussel, UMR
Chirotechnologies, Paul Cézanne University, Marseille,
France
P150.
VCD-spectroscopic
investigation of enantiopure cyclic β-lactams obtained through
Lipolase-catalysed
enantioselective enzymatic ring-opening
reaction
E. Vass, M.
Hollósi, E. Forró, F. Fülöp, Dept. of Organic Chemistry, Eötvös
Loránd University, Budapest, & Inst. of Pharmaceutical Chemistry,
University of Szeged, Szeged, Hungary
P151.
Water-soluble
calix[4]resorcarenes as enantioselective NMR shift reagents for
aromatic
compounds
T. J. Wenzel,
C. F. Dignam, J. J. Zopf, C. J. Richards, Bates College, Dept. of
Chemistry,
Lewiston, Maine,
USA
P152.
Enantioseparation
of chrysanthemic ethyl ester using cellulose benzoates as chiral
stationary
phases for HPLC
C. Yamamoto, K. Motoya, M. Kamigaito, T. Aratani,
Y. Okamoto,
Dept. of Applied Chemistry, & EcoTopia Science Inst., Nagoya
University, Nagoya, & Sumitomo Chemical Co., Osaka,
Japan
P153.
Radical
polymerization of maleimides having phenylglycine alkyl ester
derivatives and
chiroptical property of the polymers
H. Yamasaki, K. Onimura, T. Oishi, Ube National
College of Technology, & Faculty of Engineering Yamaguchi
University, Yamaguchi, Japan
P154.
The
effect of acidic and basic additives on the enantioseparation of basic
drugs on
polysaccharide-based chiral stationary phases
Y. K. Ye, Bristol-Myers Squibb Company, AR&D, New
Brunswick, NJ,
USA
P155.
Dynamic
chiral discrimination using 1,1'-binaphthyl-2,2'-diyl hydrogen
phosphates
having large p-plane
substituents at the
3,3'-positions
I. Yonemura, S. Tsukimoto, H. Ito, R. Nishida, M.
Matsuda, H.
Furuno, J. Inanaga, Dept. of Molecular Chemistry, & Institute
for
Materials Chemistry and Engineering, Kyushu University, Fukuoka,
Japan
P156.
GC-MS
analysis of amino acid enantiomers as their N(O,S)-perfluoroacyl
perfluroalkyl
esters derivatives: detection of chemical biomarkes in space analysis
M. Zampolli,
M. C. Pietrogrande, F. Dondi, R. Sternberg, F. Raulin, Dip. di
Chimica,
Universitŕ di Ferrara, Ferrara, Italy, & Lab. Interuniversitaire
des Systčmes
Atmosphériques, Université Paris 7 & Paris 12, Créteil Cedex,
France
P157.
Study
of the behaviour of D-glucose and L-glucose in aqueous solutions by
time domain
1H-NMR. Implications in biological
chirality
R. Scorei, V. M. Cimpoiasu, University of Craiova,
Craiova, Romania
P158.
Transition
metal templates in the transfer of chiral information
C. Zucchi, L. Bencze, K. Micskei, O. Holczknecht, L. Caglioti,
G. Pályi,
Dip. di Chimica, Universitŕ di Modena e Reggio Emilia, Modena, Italy
&
b. Dept. of Organic Chemistry, University of Veszprém, Veszprém, &
Dept. of
Inorganic and Analytical Chemistry, University of Debrecen, Debrecen,
Hungary,
& Dip. di Studi di Chimica e Tecnologia delle Sostanze
Biologicamente
Attive, Universitŕ “La Sapienza” , Roma, Italy
P159. Synthesis
of chiral helical quinones by oxidative
coupling of 2-hydroxy[n]helicenes Transition metal
templates in the transfer of chiral information
M. Karikomi, M.
Sudo, M. Shibuya, T.
Oba, M. Minabe, Department
of Applied Chemistry, Faculty of Engineering, Utsunomiya University,
Yoto
7-1-2, Utsunomiya 321-8585, Japan
P160. Immobilized
versus coated cellulose
tris-(3,5-dimethylphenyl--carbamate) chiral stationary phases for the
enantioselective separation of cyclopropane derivatives by liquid
chromatography
A.
Ghanem, Lahoucine Naim, Centre for
Clinical Research (MBC-03-95), King
Faisal Specialist Hospital and Research Center, Riyadh - 11211, Saudi
Arabia, &
Biomedical Analysis Department, Faculty of Pharmaceutical Sciences,
Utrecht
University, Sorbonnelaan 16, 3584 CA Utrecht, The Netherlands.
P161. Progress Towards
the Stereoselective Synthesis of
Isocyclocitrinol – A Structurally Unique C25 Steroid
A. Soheili, J. L. Leighton, University
of Columbia, Department of
Chemistry, 3000 Broadway, New York, NY 10027
P162. Separation
and quantification of N-alkylated cyclens by non-aqueous capillary zone
electrophoresis
Z. Bosáková, E. Zimmelová , P. Coufal , P.
Hermann , J.Rudovský , I. Lukeš Department
of Analytical Chemistry and b Department of Inorganic Chemistry,Faculty
of
Science, Charles University, Albertov 2030, Prague, Czech Republic
P163. Chiral Separation
of Selected Profens with Vancomycin
as Chiral Selector in Capillary Liquid Chromatography
Z.
Bosáková Eva
Tesařová , Božena Kafková , P. Coufal, J. Ševčík, Department
of Analytical Chemistry, Faculty
of Science, Charles University, Albertov 2030, 128 40 Prague 2, Czech
Republic
and Department of Physical and Macromolecular Chemistry, Faculty of
Science, Charles
University, Albertov 2030, 128 40 Prague 2, Czech Republic, and
Department of
Analytical chemistry, Faculty of Science, Palacký University, Třída
Svobody 8,
771 47 Olomouc, Czech Republic