Mild and Chemoselective Thioacylation of Amines Enabled by the Nucleophilic Activation of Elemental Sulfur
Author:
Affiliation:
1. Graduate School of Pharmaceutical Sciences, Kyoto University, Yoshida, Sakyo-ku, Kyoto 606-8501, Japan
Funder
Sumitomo Foundation
Japan Society for the Promotion of Science
Hoansha Foundation
Publisher
American Chemical Society (ACS)
Subject
Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis
Link
https://pubs.acs.org/doi/pdf/10.1021/jacs.0c03256
Reference55 articles.
1. Thioamides as Useful Synthons in the Synthesis of Heterocycles
2. From Amino Acids to Heteroaromatics—Thiopeptide Antibiotics, Nature's Heterocyclic Peptides
3. Thioamides and Thioformamides for Sequential Reactions with Organolithium and Grignard Reagents
4. Cooperative Asymmetric Catalysis Using Thioamides toward Truly Practical Organic Syntheses
5. Transition Metal‐Catalyzed C−H Bond Functionalizations by Use of Sulfur‐Containing Directing Groups
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