Stereoselective synthesis of α-linked saccharides by use of per O-benzylated 2-pyridyl 1-thio hexopyranosides as glycosyl donors and methyl iodide as an activator

DOI: 10.1016/S0040-4020(01)86571-6

Source and publish data:

Tetrahedron p. 6435 - 6448 (1991)

Update date:2022-08-02

Topics:

Authors:

Mereyala

Reddy Reddy

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Article abstract of DOI:10.1016/S0040-4020(01)86571-6

A new, practical, stereoselective glycosidation methodology is described where per O-benzylated 2-pyridyl 1-thio-α/β-hexopyranosyl donors of D-gluco-(1), D-galacto- (2), D-manno- (3) and L-rhamno- (4) configurations have been efficiently coupled with dive

Full text of DOI:10.1016/S0040-4020(01)86571-6

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Product name:2-pyridyl 2,3,6-tri-O-benzyl-4-O-(2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl)-1-thio-β-D-glucopyranoside

Cas No:139391-15-4

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