Issue 0, 1967

Cyclitols. Part XXIV. Selective acetolysis of myoinositol benzyl ethers

Abstract

The acetolysis of benzyl ethers of myoinositol is selective and its rate varies with the nature and configuration of the neighbouring groups. The penta-acetate of 1-O-benzylmyoinositol is readily obtained from 1,4,5,6-tetra-O-benzylmyoinositol; hydrogenolysis gives 1,2,4,5,6-penta-O-acetylmyoinositol.

Article information

Article type
Paper

J. Chem. Soc. C, 1967, 919-922

Cyclitols. Part XXIV. Selective acetolysis of myoinositol benzyl ethers

S. J. Angyal, M. H. Randall and M. E. Tate, J. Chem. Soc. C, 1967, 919 DOI: 10.1039/J39670000919

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