Solvent-controlled regioselective protection of allyl-4,6-benzylidene glucopyranosides.

ABSTRACT: We wish to report a simple synthetic procedure, which permits the regiospecific mono-acylation, alkylation and silylation at the 2-position of allyl 4,6-O-benzylidene alpha-D-glucopyranoside in high yields and which does not require the use of catalysts.

SUBMITTER: Ness KA 

PROVIDER: S-EPMC2048501 | biostudies-literature | 2007 Sep

REPOSITORIES: biostudies-literature