|
This article is cited in 4 scientific papers (total 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.
Citation:
A. G. Tolstikov, E. E. Savateeva, L. V. Spirikhin, G. A. Tolstikov, “New Chirones Prepared from 2-Acetoxyglucal”, Mendeleev Commun., 1:4 (1991), 133–134
Linking options:
https://www.mathnet.ru/eng/mendc5543 https://www.mathnet.ru/eng/mendc/v1/i4/p133
|
|
Contact us: