An extremely mild and general method for the construction of 1,2-trans- β-glycosidic linkages via glycopyranosyl diethyl phosphites with participating groups at C-2

DOI: 10.1248/cpb.43.2267

Source and publish data:

Chemical and Pharmaceutical Bulletin p. 2267 - 2269 (1995)

Update date:2022-08-11

Topics:

Authors:

Hashimoto

Sano Sano

Umeo Umeo

Nakajima

Ikegami Ikegami

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Article abstract of DOI:10.1248/cpb.43.2267

A highly efficient 1,2-trans-β-glycosidation reaction has been developed by using glycopyranosyl diethyl phosphites bearing participating groups such as benzoate, phthalimido, or trichloroethyl carbamate groups at C-2 as glycosyl donors and trimethylsilyl

Full text of DOI:10.1248/cpb.43.2267

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