Issue 2, 1988

Ring opening of 2,3-, 3,4-, and 4,6-O-benzylidene acetals of pyranosides by photobromination with bromotrichloromethane

Abstract

2,3- 3,4-, and 4,6-O-Benzylidene pyranoside derivatives on photobromination in bromotrichloromethane yield bromo-deoxy-pyranoside benzoates regio- and stereo-specifically which, for the acyl derivatives of the 2,3- and 3,4-acetals, is superior to their reaction with N-bromosuccinimide.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1988, 94-96

Ring opening of 2,3-, 3,4-, and 4,6-O-benzylidene acetals of pyranosides by photobromination with bromotrichloromethane

J. S. Chana, P. M. Collins, F. Farnia and D. J. Peacock, J. Chem. Soc., Chem. Commun., 1988, 94 DOI: 10.1039/C39880000094

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