Ozonolysis of Acetals. (1) Ester Synthesis, (2) THP Ether Cleavage, (3) Selective Oxidation of β-Glycoside, (4) Oxidative Removal of Benzylidene and Ethylidene Protecting Groups
- 15 July 1971
- journal article
- Published by Canadian Science Publishing in Canadian Journal of Chemistry
- Vol. 49 (14) , 2465-2467
- https://doi.org/10.1139/v71-405
Abstract
Ozone reacts very smoothly with acetals to give the corresponding esters. Tetrahydropyranyl ethers, β-glycopyranosides, ethylidene, or benzylidene derivatives are also oxidized whereas the α-glycopyranosides are inert.Keywords
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