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
A redox-neutral palladium(II)-catalyzed conversion of aryl, heteroaryl, and alkenyl boronic acids in...
A redox-neutral palladium(II)-catalyzed conversion of aryl, heteroaryl, and alkenyl boronic acids in...
The palladium-catalyzed three-component coupling of aryl iodides, sulfur dioxide, and hydrazines to ...
A palladium-catalysed aminosulfonylation process is used as the key-step in a one-pot, three-compone...
A mild, efficient synthesis of sulfonyl fluorides from aryl and heteroaryl bromides utilizing pallad...
A mild, efficient synthesis of sulfonyl fluorides from aryl and heteroaryl bromides utilizing pallad...
We describe a method for the synthesis of sulfonamides through the combination of an organometallic ...
Sulfonyl-derived functional groups populate a broad range of useful molecules and materials, and des...
A novel palladium-catalyzed sulfination of aryl and heteroaryl halides is described. This reaction o...
Sulfonyl-derived functional groups populate a broad range of useful molecules and materials, and des...
The coupling of carboxylic acids and amines to form amide linkages is the most commonly performed re...
A one-pot Pd-catalyzed conversion of aryl iodide to aryl sulfonyl fluorides using DABSO and Selectfl...
A palladium-catalyzed method for the preparation of sulfonamides is described. The process exhibits ...
First introduced into medicines in the 1930s, the sulfonamide functional group continues to be prese...
A one-pot process for the synthesis of unsymmetrical sulfoxides using organometallic nucleophiles is...
A redox-neutral palladium(II)-catalyzed conversion of aryl, heteroaryl, and alkenyl boronic acids in...
A redox-neutral palladium(II)-catalyzed conversion of aryl, heteroaryl, and alkenyl boronic acids in...
The palladium-catalyzed three-component coupling of aryl iodides, sulfur dioxide, and hydrazines to ...
A palladium-catalysed aminosulfonylation process is used as the key-step in a one-pot, three-compone...
A mild, efficient synthesis of sulfonyl fluorides from aryl and heteroaryl bromides utilizing pallad...
A mild, efficient synthesis of sulfonyl fluorides from aryl and heteroaryl bromides utilizing pallad...
We describe a method for the synthesis of sulfonamides through the combination of an organometallic ...
Sulfonyl-derived functional groups populate a broad range of useful molecules and materials, and des...
A novel palladium-catalyzed sulfination of aryl and heteroaryl halides is described. This reaction o...
Sulfonyl-derived functional groups populate a broad range of useful molecules and materials, and des...
The coupling of carboxylic acids and amines to form amide linkages is the most commonly performed re...
A one-pot Pd-catalyzed conversion of aryl iodide to aryl sulfonyl fluorides using DABSO and Selectfl...
A palladium-catalyzed method for the preparation of sulfonamides is described. The process exhibits ...
First introduced into medicines in the 1930s, the sulfonamide functional group continues to be prese...
A one-pot process for the synthesis of unsymmetrical sulfoxides using organometallic nucleophiles is...
A redox-neutral palladium(II)-catalyzed conversion of aryl, heteroaryl, and alkenyl boronic acids in...
A redox-neutral palladium(II)-catalyzed conversion of aryl, heteroaryl, and alkenyl boronic acids in...
The palladium-catalyzed three-component coupling of aryl iodides, sulfur dioxide, and hydrazines to ...