Preparation and Application of α-Imino Ketones through One-Pot Tandem Reactions Based on Heyns Rearrangement
Author:
Affiliation:
1. College of Chemical Engineering, Sichuan University, Chengdu, Sichuan 610065, P.R. China
2. Natural Products Research Center Chengdu Institution of Biology Chinese Academy of Science, Chengdu, Sichuan 610041, P.R. China
Funder
West Light Foundation of the Chinese Academy of Sciences
Youth Innovation Promotion Association of the Chinese Academy of Sciences
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.1c02390
Reference44 articles.
1. Brønsted Base‐Catalyzed Formal Reductive [3+2] Annulation of 4,4,4‐Trifluorocrotonate and α‐Iminoketones
2. CBr4-mediated cross-coupling reactions of α-amino carbonyl compounds with alcohols and thiols to build C–O and C–S bonds, respectively
3. New β-amino-α-trifluoromethyl alcohols and their exploration in the synthesis of trifluoromethylated imidazole derivatives
4. Nucleophilic addition of (difluoromethyl)trimethylsilane to selected α-imino ketones and aryl diketones
5. CuI-catalyzed and air promoted oxidative cyclization for one-pot synthesis of polyarylated oxazoles
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