Decarboxylative Generation of 2-Azaallyl Anions: 2-Iminoalcohols via a Decarboxylative Erlenmeyer Reaction
Author:
Affiliation:
1. Key Laboratory of Green Chemistry & Technology, College of Chemistry, Sichuan University, Chengdu, Sichuan 610064, P. R. China
2. Department of Chemistry, University of Virginia, Charlottesville, Virginia 22904-4319, United States
Funder
Thomas F. and Kate Miller Jeffress Memorial Trust
National Natural Science Foundation of China
University of Virginia Institute on Aging
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.5b00107
Reference38 articles.
1. Transition Metal-Catalyzed Decarboxylative Allylation and Benzylation Reactions
2. C−C Bond-Forming Reactions via Pd-Mediated Decarboxylative α-Imino Anion Generation
3. One-Pot Tandem Decarboxylative Allylation−Heck Cyclization of Allyl Diphenylglycinate Imines: Rapid Access to Polyfunctionalized 1-Aminoindanes
4. Palladium-Catalyzed Decarboxylative Generation and Asymmetric Allylation of α-Imino Anions
5. Tandem C−C Bond-Forming Processes: Interception of the Pd-Catalyzed Decarboxylative Allylation of Allyl Diphenylglycinate Imines with Activated Olefins
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