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JOURNALS // Mendeleev Communications // Archive

Mendeleev Commun., 2005 Volume 15, Issue 4, Pages 140–141 (Mi mendc3715)

This article is cited in 30 papers

Chirality-directed organogel formation

R. G. Kostyanovsky, D. A. Lenev, O. N. Krutius, A. A. Stankevich

N.N. Semenov Federal Research Center for Chemical Physics, Russian Academy of Sciences, Moscow, Russian Federation

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.

Language: English

DOI: 10.1070/MC2005v015n04ABEH002136



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