Formation of meta-Substituted Phenols by Transition Metal-Free Aromatization: Use of 2-Bromocyclohex-2-en-1-ones
Author:
Affiliation:
1. Chemistry Department, University of Alberta, Edmonton, Alberta T6G 2G2, Canada
Funder
Natural Sciences and Engineering Research Council of Canada
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.joc.6b01653
Reference57 articles.
1. Synthesis of Substituted Resorcinol Monomethyl Ethers from 2-Bromo-3-methoxycyclohex-2-en-1-ones
2. A Family of Routes to Substituted Phenols, Including Meta-Substituted Phenols
3. Efficient Microwave-Assisted Pd-Catalyzed Hydroxylation of Aryl Chlorides in the Presence of Carbonate
4. Aerobic Oxidative Heck/Dehydrogenation Reactions of Cyclohexenones: Efficient Access tometa-Substituted Phenols
5. Room-Temperature meta-Functionalization: Pd(II)-Catalyzed Synthesis of 1,3,5-Trialkenyl Arene and meta-Hydroxylated Olefin
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