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A Novel Glycosylation Reaction of 2-Amino-2-deoxy-D-glucopyranose Using Dimethylphosphinothioate

DOI: 10.1246/cl.1989.69

Source and publish data:

Chemistry Letters p. 69 - 72 (1989)

Update date:2022-09-26

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Authors:

Inazu, ToshiyukiInazu, Toshiyuki

Yamanoi, TakashiYamanoi, Takashi

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Article abstract of DOI:10.1246/cl.1989.69

β-Glucosides were stereoselectively obtained in good yields from 3,4,6-tri-O-benzyl-2-benzyloxycarbonylamino-2-deoxy-α-D-glucopyranosyl dimethylphosphinothioate with several alcohols in the presence of iodine and a catalytic amount of trityl or perchlorat

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Full text of DOI:10.1246/cl.1989.69

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Product name:[(2R,3R,4R,5S,6R)-4,5-Bis-benzyloxy-6-benzyloxymethyl-2-((2R,3R,4S,5R,6S)-3,4,5-tris-benzyloxy-6-methoxy-tetrahydro-pyran-2-ylmethoxy)-tetrahydro-pyran-3-yl]-carbamic acid benzyl ester

Cas No:121682-64-2

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