One-Pot Synthesis of Sulfonamides from Unactivated Acids and Amines via Aromatic Decarboxylative Halosulfonylation
Author:
Affiliation:
1. Merck Center for Catalysis, Princeton University, Princeton, New Jersey 08544, United States
2. Worldwide Research and Development, Pfizer, Inc., Eastern Point Road, Groton, Connecticut 06340, United States
Funder
Princeton University
Genentech
Division of Graduate Education
Pfizer
Bristol-Myers Squibb
National Institute of General Medical Sciences
Merck
Janssen Pharmaceuticals
Princeton Catalysis Initiative
Publisher
American Chemical Society (ACS)
Subject
Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis
Link
https://pubs.acs.org/doi/pdf/10.1021/jacs.3c08218
Reference72 articles.
1. Decarboxylative Halogenation of Organic Compounds
2. Carboxylic Acids as Adaptive Functional Groups in Metallaphotoredox Catalysis
3. What is in Our Kit? An Analysis of Building Blocks Used in Medicinal Chemistry Parallel Libraries
4. Expanding the medicinal chemistry synthetic toolbox
5. The Formal Cross‐Coupling of Amines and Carboxylic Acids to Form sp 3 –sp 3 Carbon–Carbon Bonds
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