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Chirality-directed organogel formation

Remir Grigorevich Kostyanovsky 1
Remir Grigorevich Kostyanovsky
Denis Alekseevich Lenev 1
Denis Alekseevich Lenev
Oleg Nikolaevich Krutius 1
Oleg Nikolaevich Krutius
Andrey Aleksandrovich Stankevich 1
Andrey Aleksandrovich Stankevich
Published 2005-06-28
CommunicationVolume 15, Issue 4, 140-141
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Kostyanovsky R. G. et al. Chirality-directed organogel formation // Mendeleev Communications. 2005. Vol. 15. No. 4. pp. 140-141.
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Kostyanovsky R. G., Lenev D. A., Krutius O. N., Stankevich A. A. Chirality-directed organogel formation // Mendeleev Communications. 2005. Vol. 15. No. 4. pp. 140-141.
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TY - JOUR
DO - 10.1070/MC2005v015n04ABEH002136
UR - https://mendcomm.colab.ws/publications/10.1070/MC2005v015n04ABEH002136
TI - Chirality-directed organogel formation
T2 - Mendeleev Communications
AU - Kostyanovsky, Remir Grigorevich
AU - Lenev, Denis Alekseevich
AU - Krutius, Oleg Nikolaevich
AU - Stankevich, Andrey Aleksandrovich
PY - 2005
DA - 2005/06/28
PB - Mendeleev Communications
SP - 140-141
IS - 4
VL - 15
ER -
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@article{2005_Kostyanovsky,
author = {Remir Grigorevich Kostyanovsky and Denis Alekseevich Lenev and Oleg Nikolaevich Krutius and Andrey Aleksandrovich Stankevich},
title = {Chirality-directed organogel formation},
journal = {Mendeleev Communications},
year = {2005},
volume = {15},
publisher = {Mendeleev Communications},
month = {Jun},
url = {https://mendcomm.colab.ws/publications/10.1070/MC2005v015n04ABEH002136},
number = {4},
pages = {140--141},
doi = {10.1070/MC2005v015n04ABEH002136}
}
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Kostyanovsky, Remir Grigorevich, et al. “Chirality-directed organogel formation.” Mendeleev Communications, vol. 15, no. 4, Jun. 2005, pp. 140-141. https://mendcomm.colab.ws/publications/10.1070/MC2005v015n04ABEH002136.

Abstract

New low molecular mass enantiopure organogelators (1R,4R)-1, (S)-2, (R)-3 and (R)-4 were found; racemates (R,S)-3 and (R,S)-4 have only a moderate gelating power, whereas (R,S)-1 and (R,S)-2 do not show gelating properties at all.

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