A general and mild two-step procedure for the synthesis of aryl and heteroaryl sulfonamides from the corresponding iodides
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference8 articles.
1. An enantioselective synthesis of sulphonamide hydroxamic acids as matrix metalloproteinase inhibitors
2. Synthesis of Functional Aromatic Multisulfonyl Chlorides and Their Masked Precursors
3. Direct Conversion of Thiols to Sulfonyl Chlorides and Sulfonamides
4. Sulfonyl Chloride Formation from Thiol Derivatives by N-Chlorosuccinimide Mediated Oxidation
5. Convenient One‐Pot Synthesis of Sulfonamides from Thiols using Trichloroisocyanuric Acid
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