Palladium(0)-Catalyzed Intermolecular Asymmetric Allylic Dearomatization of Substituted β-Naphthols with Morita–Baylis–Hillman (MBH) Adducts
Author:
Affiliation:
1. State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, University of Chinese Academy of Sciences, Chinese Academy of Sciences, 345 Lingling Lu, Shanghai, 200032, China
Funder
Ministry of Science and Technology of the People's Republic of China
Science and Technology Commission of Shanghai Municipality
National Natural Science Foundation of China
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.2c03262
Reference60 articles.
1. Transition-Metal-Catalyzed Asymmetric Allylic Dearomatization Reactions
2. Asymmetric dearomatization of phenols
3. Catalytic asymmetric dearomatization (CADA) reactions of phenol and aniline derivatives
4. Gold-catalyzed Dearomatization Reactions
5. Recent Developments in Transition Metal‐Catalyzed Dearomative Cyclizations of Indoles as Dipolarophiles for the Construction of Indolines
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