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JOURNALS // Mendeleev Communications // Archive

Mendeleev Commun., 1991 Volume 1, Issue 4, Pages 133–134 (Mi mendc5543)

This article is cited in 4 papers

New Chirones Prepared from 2-Acetoxyglucal

A. G. Tolstikova, E. E. Savateevab, L. V. Spirikhinb, G. A. Tolstikovc

a G.K. Boreskov Institute of Catalysis, Siberian Branch of the Russian Academy of Sciences, Novosibirsk, Russian Federation
b Ufa Institute of Chemistry, Ufa Federal Research Centre of the Russian Academy of Sciences, Ufa, Russian Federation
c N.N. Vorozhtsov Novosibirsk Institute of Organic Chemistry, Siberian Branch of the Russian Academy of Sciences, Novosibirsk, Russian Federation

Abstract: Reaction of 2,3,4,6-tetra-O-acetyl-D-glucal with allyltrimethylsilane, methyl 3-mercaptopropionate, methyl (6R)-6-benzoyloxy-7-oxyheptanoate or glycolic acid methyl ester, catalysed by boron trifluride etherate, leads preferentially to the a-anomers of unsaturated 2’-oxo-C-, S- or O-glycosides.

Language: English

DOI: 10.1070/MC1991v001n04ABEH000082



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