Author:
Dadson William M.,Hutchinson John H.,Money Thomas
Abstract
Evidence is presented to support the occurrence of a 3,2-endo-methyl shift during the C(8)-bromination of 3,3-dibromocamphor. The mechanism proposed for the rearrangement of (+)-3-bromocamphor to (−)-6-bromocamphor is also supported by experimental evidence. Keywords: 8-bromocamphor, 6-bromocamphor, 3,2-endo methyl shifts.
Publisher
Canadian Science Publishing
Subject
Organic Chemistry,General Chemistry,Catalysis
Cited by
11 articles.
订阅此论文施引文献
订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献