One-pot sulfonamide synthesis exploiting the palladium-catalyzed sulfination of aryl iodides

Symplectic ID
592480
Source
Ora (Hyrax)
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Saturday, 4 July, 2026 - 22:12
DOI
10.1055/s-0035-1560578
Publication Date
Tuesday, 13 October, 2015
First Page
101
Last Page
105
Keywords
amines
aryl halides
sulfinates
sulfonamides
palladium catalysis
Authors
Flegeau, EF
Harrison, JM
Willis, MC
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0
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Abstract
Aryl ammonium sulfinates, conveniently prepared from aryl iodides and the sulfur dioxide surrogate DABSO, under the action of a Pd(0) catalyst, are transformed in a onepot process to a variety of functionalized sulfonamides. The sulfinate to sulfonamide transformation is achieved by simple treatment with an aqueous solution of the relevant amine and sodium hypochlorite (bleach). A broad range of amines, including anilines, and amino acids derivatives, are combined efficiently with a variety of aryl iodides, leading to sulfonamides in high yields.
Publisher
Thieme
ISSN
0936-5214
Journal Title
SYNLETT
eISSN
1437-2096
Volume
27
Issue
1
ID at Source
uuid_0f18a0aa-1e8e-4bd1-85c3-17e74f90e262
Publication Status
Published
Open access
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chem0368