Oxidative Rearrangement of Tertiary Allylic Alcohols Employing Oxoammonium Salts
Author:
Affiliation:
1. Department of Organic Chemistry, Graduate School of Pharmaceutical Sciences, Tohoku University, Aobayama, Sendai 980-8578, Japan
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo800634r
Reference57 articles.
1. Direct oxidation of tertiary allylic alcohols. A simple and effective method for alkylative carbonyl transposition
2. Oxidative rearrangements of tertiary and some secondary allylic alcohols with chromium(VI) reagents. A new method for 1,3-functional group transposition and forming mixed aldol products
3. Metal-Mediated Oxidation of Tertiary Alcohols and Related Fragmentations
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