Literature DB >> 12000272

Highly stereoselective ring-opening addition of terminal acetylenes to bicyclic olefins catalyzed by nickel complexes.

Dinesh Kumar Rayabarapu1, Chii-Feng Chiou, Chien-Hong Cheng.   

Abstract

[reaction: see text] Treatment of 7-oxa- and 7-azabenzonorbornadienes with terminal acetylenes in the presence of Ni(dppe)Cl2, ZnCl2, and Zn powder in toluene at 90 degrees C afforded the corresponding cis-2-alkynyl-1,2-dihydronaphthalene derivatives in moderate to excellent yields with remarkably high stereoselectivity.

Entities:  

Year:  2002        PMID: 12000272     DOI: 10.1021/ol025731d

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  1 in total

1.  Iridium-catalyzed asymmetric ring-opening reactions of azabenzonorbornadiene with carboxylic acid nucleophiles.

Authors:  Yuhua Long; Wenling Wang; Dingqiao Yang; Han Jiang; Kaixuan Chen; Yali Fang
Journal:  Mol Divers       Date:  2013-11-27       Impact factor: 2.943

  1 in total

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