Literature DB >> 21314095

Pd(0)-catalyzed [1,5]-sigmatropic hydrogen shift of propargylic esters toward substituent naphthylamines.

Shu-Chun Zhao1, Xing-Zhong Shu, Ke-Gong Ji, An-Xi Zhou, Ting He, Xue-Yuan Liu, Yong-Min Liang.   

Abstract

A novel and convenient carboannulation method for the synthesis of highly substituted naphthylamine derivatives has been developed though a Pd(0)-catalyzed [1,5]-sigmatropic hydrogen shift and cyclization reaction of propargyl esters.

Entities:  

Year:  2011        PMID: 21314095     DOI: 10.1021/jo1024267

Source DB:  PubMed          Journal:  J Org Chem        ISSN: 0022-3263            Impact factor:   4.354


  1 in total

1.  Nickel-catalyzed cyclization of alkyne-nitriles with organoboronic acids involving anti-carbometalation of alkynes.

Authors:  Xingjie Zhang; Xin Xie; Yuanhong Liu
Journal:  Chem Sci       Date:  2016-05-19       Impact factor: 9.825

  1 in total

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