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1.
Org Biomol Chem ; 14(2): 590-597, 2016 Jan 14.
Artigo em Inglês | MEDLINE | ID: mdl-26531097

RESUMO

A new synthesis of sulfonamides has been developed via an iodine-catalyzed sulfonylation of amines with arylsulfonyl hydrazides. This metal-free strategy employs readily accessible and easy to handle starting materials, catalysts and oxidants, and can be easily conducted under mild conditions, providing a convenient access to a wide range of sulfonamides in moderate to excellent yields within a short reaction time.

2.
J Org Chem ; 80(7): 3447-54, 2015 Apr 03.
Artigo em Inglês | MEDLINE | ID: mdl-25791508

RESUMO

A highly efficient iodine-catalyzed regioselective oxidative cross-coupling of an indole C-H bond and azole N-H bond is described. This metal-free reaction can be easily carried out at room temperature under mild and environmentally friendly conditions and provides a series of N-linked 2-(azol-1-yl)indole derivatives in moderate to excellence yields.


Assuntos
Azóis/química , Indóis/síntese química , Iodo/química , Catálise , Indóis/química , Estrutura Molecular , Oxirredução , Estereoisomerismo
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