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2003, Volume 13, Issue 3  


Louis Pasteur did it for us especially
R. G. Kostyanovsky
85–90
Eternal dissymmetry
M. Hargittai, I. Hargittai
91–92
The reexamination of Pasteur's experiment in Japan
Y. Tobe
93–94
Resolution of Pasteur salts by auto-seeded preferential crystallization
M.-N. Petit, G. Coquerel
95–96
Pasteur-like resolution of quasi-racemates in solid and gas phases
R. G. Kostyanovsky, E. N. Nikolaev, O. N. Kharybin, G. K. Kadorkina, V. R. Kostyanovsky
97–99
Spontaneous resolution of a non-degenerate donor—acceptor [2]catenane
E. Alcalde, L. Pérez-García, S. Ramos, J. F. Stoddart, S. A. Vignon, A. J. White, D. J. Williams
100–102
Generation of an optically active rhodium(III) complex by crystallization-induced spontaneous resolution of a racemic mixture
I. L. Odinets, O. I. Artyushin, E. V. Sharova, E. I. Goryunov, D. G. Golovanov, K. A. Lyssenko, P. V. Petrovskii, T. A. Mastryukova
102–104
Systematic search for conglomerates among glycerol aromatic monoethers: guaifenesin and mephenesin are the cases
A. A. Bredikhin, Z. A. Bredikhina, S. N. Lazarev, D. V. Savel'ev
104–105
A new conglomerate in a series of 2,3:6,7-dibenzobicyclo[3.3.1]nonanes
P. A. Levkin, K. A. Lyssenko, V. Schurig, R. G. Kostyanovsky
106–108
Crystal structure and magnetic properties of novel chiral nitroxides existing as racemic conglomerates
N. Ikuma, R. Tamura, S. Shimono, N. Kawame, O. Tamada, N. Sakai, J. Yamauchi, Y. Yamamoto
109–111
Asymmetric three-coordinated nitrogen compounds: spontaneous resolution and absolute asymmetric synthesis
R. G. Kostyanovsky, V. R. Kostyanovsky, G. K. Kadorkina, K. A. Lyssenko
111–113
Spontaneous resolution in the imidazolidin-2-one series
A. N. Kravchenko, G. K. Kadorkina, A. S. Sigachev, E. Yu. Maksareva, K. A. Lyssenko, P. A. Belyakov, O. V. Lebedev, O. N. Kharybin, N. N. Makhova, R. G. Kostyanovsky
114–116
2-Phenyl-3-hydroxyimidazolidin-4-one: the regioselective synthesis, structure and enantiomerically enriched crystallization
I. V. Vystorop, K. A. Lyssenko, R. G. Kostyanovsky
116–118
Crystal structure of a new racemate showing Preferential Enrichment: evidence for the existence as a racemic mixed crystal composed of the two enantiomers
H. Takahashi, R. Tamura, Sh. Yabunaka, T. Ushio
119–121
The first chiral derivatives of 1-boraadamantane
M. E. Gurskii, V. A. Ponomarev, K. A. Lyssenko, M. Yu. Antipin, Ph. Renaud, Yu. N. Bubnov
121–123
Efficient resolution of (±)-α-cyclopropylethanol by crystallization of its inclusion complex with chiral diols
M. G. Vinogradov, D. V. Kurilov, G. V. Chel'tsova, V. A. Ferapontov, G. Heise
124–125
Efficient resolution of rac-2,3-O-isopropylideneglycerol by enantioselective inclusion crystallization with the chiral diol CYTOL
M. G. Vinogradov, D. V. Kurilov, V. A. Ferapontov, G. Heise
125–126
Chemoenzymatic synthesis of optically active phosphinic analogues of S-substituted sulfur-containing amino acids
K. V. Alferov, Yu. N. Zhukov, N. G. Faleev, E. N. Khurs, R. M. Khomutov
127–128
Theory of hierarchical chiral asymmetry
D. Kondepudi
128–129
Parity-violating energy difference between enantiomers: recent developments
L. Keszthelyi
129–130
The effect of β-particles on the crystallization of 1,1′-binaphthyl and 4,4′-dimethylchalcone
R. Sullivan, N. Conley, R. N. Compton, R. M. Pagni
131–132
Asymmetric synthesis of unusual α-amino acids
Yu. N. Belokon, K. A. Kochetkov, D. A. Borkin
132–134
Chiral P*-monodentate phosphite ligand for Pd-catalysed asymmetric allylation reactions
K. N. Gavrilov, V. N. Tsarev, S. E. Lyubimov, A. A. Shiryaev, S. V. Zheglov, O. G. Bondarev, V. A. Davankov, A. A. Kabro, S. K. Moiseev, V. N. Kalinin
134–136
Nitrogen chirality via the sterical veto of N inversion
S. V. Usachev, G. A. Nikiforov, Yu. A. Strelenko, I. I. Chervin, K. A. Lyssenko, R. G. Kostyanovsky
136–139
Induction of chirality in donor–acceptor spiro compounds
M. Kwit, J. Gawronski
139–140
Chiral switching and fast reversible molecular movement phenomena in crystals
Sh. Hirano, K. Yoshizawa, Sh. Toyota, F. Toda, Z. Urbanczyk-Lipkowska
141–144
Comparison of the X-ray structures of concomitant pseudodimorphs formed between a diquinoline host and d-chloroform guest
J. Ashmore, R. L. Bishop, D. C. Craig, M. L. Scudder
144–146
New double-stranded helicate based on a chiral bis(bipyridine)-type chelator
B. Quinodoz, H. Stoeckli-Evans, A. von Zelewsky
146–147
Spontaneous rearrangement of hydrogen bonding in a crystalline state
R. Kuroda, Y. Imai
148–149
A stereochemical approach to the Kabachnik–Fields reaction mechanism
M. N. Dimukhametov, E. V. Bayandina, E. Yu. Davydova, A. T. Gubaidullin, V. A. Alfonsov
150–151
Chiral synthetic block based on (R)-pantolactone
F. A. Akbutina, I. F. Sadretdinov, N. K. Selezneva, M. S. Miftakhov
151–152
A ‘substrate-divergent’ approach to chiral cyclopentanes and cyclohexanes from a common precursor based on levoglucosan
R. V. Bikbulatov, F. A. Akbutina, L. V. Spirikhin, M. S. Miftakhov
153–154
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