Oxidative Rearrangement of Cyclic Tertiary Allylic Alcohols with IBX in DMSO
Author:
Affiliation:
1. Graduate School of Pharmaceutical Sciences, Tohoku University, Aobayama, Sendai 980-8578, Japan
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ol048210u
Reference37 articles.
1. A Facile Method for the Bishomologation of Ketones to α,β-Unsaturated Aldehydes: Application to the Synthesis of the Cyclohexanoid Components of the Boll Weevil Sex Attractant
2. Direct oxidation of tertiary allylic alcohols. A simple and effective method for alkylative carbonyl transposition
3. 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
4. Total Synthesis of (+)-Phomactin A Using a B-Alkyl Suzuki Macrocyclization
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