An extremely mild and stereocontrolled construction of 1,2-trans-β-glycosidic linkages capitalizing on benzyl-protected glycopyranosyl diethyl phosphites as glycosyl donors

DOI: 10.1016/0040-4039(95)00263-C

Source and publish data:

Tetrahedron Letters p. 2251 - 2254 (1995)

Update date:2022-07-30

Topics:

Authors:

Hashimoto, Shun-Ichi

Umeo, Kazuhiro

Sano, Ai

Watanabe, Nobuhide

Nakajima, Makoto

Ikegami, Shiro

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Article abstract of DOI:10.1016/0040-4039(95)00263-C

A highly stereocotrolled 1,2-trans-β-glycosidation reaction without neighboring group participation has been developed by using benzyl-protected glycopyranosyl diethyl phosphites as glycosyl donors and boron trifluoride etherate as a promoter. The present

Full text of DOI:10.1016/0040-4039(95)00263-C

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