Issue 11, 1976

Complete regiospecificity in the benzylation of a cis-diol by the stannylidene procedure

Abstract

While conventional monobenzylation of benzyl 6-O-allyl-2-O-benzyl-α-D-galactopyranoside (1) gives a four component mixture, treatment of the OO′-dibutyl-stannylidene derivative of (1) with benzyl bromide provides only the 3-O-benzyl ether (2) in 66% isolated yield.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1976, 375-376

Complete regiospecificity in the benzylation of a cis-diol by the stannylidene procedure

C. Augé, S. David and A. Veyrières, J. Chem. Soc., Chem. Commun., 1976, 375 DOI: 10.1039/C39760000375

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