Literature DB >> 21666924

Synthesis of 3-(aminomethylene)-2-oxoindolines by palladium-catalyzed annulation of 3-chloro-2-iodo-N-arylacrylamides with amides or amines.

Guo-Bo Deng1, Zhi-Qiang Wang, Ren-Jie Song, Ming-Bo Zhou, Wen-Ting Wei, Peng Xie, Jin-Heng Li.   

Abstract

A new palladium-catalyzed C-H bond activation-annulation-amination tandem method was presented for selectively synthesizing 3-(aminomethylene)-2-oxoindolines. In the presence of Pd(dba)(2), xantphos (L8), AgOAc and Na(2)CO(3), a variety of 3-chloro-2-iodo-N-arylacrylamides underwent the reaction with amides or amines to afford the corresponding 3-(aminomethylene)-2-oxoindolines in moderate to good yields.

Entities:  

Mesh:

Substances:

Year:  2011        PMID: 21666924     DOI: 10.1039/c1cc11602a

Source DB:  PubMed          Journal:  Chem Commun (Camb)        ISSN: 1359-7345            Impact factor:   6.222


  1 in total

1.  Bronsted acid-catalyzed rapid enol-ether formation of 2-hydroxyindole-3-carboxaldehydes.

Authors:  Darian Blanchard; T Stanley Cameron; Mukund Jha
Journal:  Mol Divers       Date:  2013-08-15       Impact factor: 2.943

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.