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Эта публикация цитируется в 2 научных статьях (всего в 2 статьях)
Hexa-O-acetyl-D-gentiobial in enantioselective synthesis of lysocerebrosides and their conjugates
A. G. Tolstikova, O. V. Tolstikovab, G. A. Tolstikovb
a G.K. Boreskov Institute of Catalysis, Siberian Branch of the Russian Academy of Sciences, Novosibirsk, Russian Federation
b N.N. Vorozhtsov Novosibirsk Institute of Organic Chemistry, Siberian Branch of the Russian Academy of Sciences, Novosibirsk, Russian Federation
Аннотация:
Hexa-O-acetyl-D-gentiobial 1 and its decyclization product (2E,4S,5R)-4-acetoxy-5-hydroxy-6-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyloxy)hex-2-enal 2 have been used to synthesize O-glycosylated aminodiols 9,10,15 that model the structure of natural lysocerebrosides. Compounds 9,10,15 can serve as basic components to produce N-acylated conjugates with derivatives of arachidonic and glycyrrhizic acids.
Образцы ссылок на эту страницу:
https://www.mathnet.ru/rus/mendc4945
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