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Эта публикация цитируется в 5 научных статьях (всего в 5 статьях)
A Convenient Approach to the Synthesis of Glycosphingolipids via the Acidic Decyclization of Hexo-O-acetyl-D-gentiobial
A. G. Tolstikova, O. F. Prokopenkob, R. Kh. Yamilovb, 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
Аннотация:
The mercury sulphate catalysed acidic opening of the dihydropyran ring in hexa-O-acetyl-D-gentiobial 2, resulting in (2E,4S,5R)-4-acetoxy- 5-hydroxy-6-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyloxy)hex-2-enal 3 was employed as the key transformation in the synthesis of O-glycosides, which are precursors of glycosphingolipids.
Образцы ссылок на эту страницу:
https://www.mathnet.ru/rus/mendc5499
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