Cyclitols. Part XXIV. Selective acetolysis of myoinositol benzyl ethers
化学
有机化学
作者
S. J. Angyal,M. H. Randall,M. E. Tate
出处
期刊:Journal of the Chemical Society. C.Organic [The Royal Society of Chemistry] 日期:1967-01-01卷期号:: 919-919被引量:9
标识
DOI:10.1039/j39670000919
摘要
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.