Intramolecular Cyclization of 3,4-Epoxy Alcohols; Oxetane Formation
- 1 May 1977
- journal article
- Published by Oxford University Press (OUP) in Bulletin of the Chemical Society of Japan
- Vol. 50 (5) , 1226-1231
- https://doi.org/10.1246/bcsj.50.1226
Abstract
1-(2,3-Epoxypropyl)-1-cyclohexanol (1) and its methyl analogues (2 and 3), when treated with base in 75% aqueous dimethyl sulfoxide, gave the corresponding oxetanes (9–11) as the main products, while treatment of compound 1 under anhydrous conditions afforded the oxolane dimer (17) as the sole identified product.This publication has 27 references indexed in Scilit:
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