Literature DB >> 12397982

Nickel-catalysed addition of organoboronates to 1,3-dienes.

Eiji Shirakawa1, Go Takahashi, Teruhisa Tsuchimoto, Yusuke Kawakami.   

Abstract

Aryl- and alkenylboronates were found to add to 1,3-dienes in the presence of a catalytic amount of bis(1,5-cyclooctadiene)nickel, where a proton source in combination with a solvent considerably controls the regioselectivity.

Entities:  

Year:  2002        PMID： 12397982     DOI： 10.1039/b207185a

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


  3 in total

1.  Ni(0)-catalyzed 1,4-selective diboration of conjugated dienes.

Authors:  Robert J Ely; James P Morken
Journal:  Org Lett       Date:  2010-10-01       Impact factor: 6.005

2.  Regio- and stereoselective Ni-catalyzed 1,4-hydroboration of 1,3-dienes: access to stereodefined (Z)-allylboron reagents and derived allylic alcohols.

Authors:  Robert J Ely; James P Morken
Journal:  J Am Chem Soc       Date:  2010-03-03       Impact factor: 15.419

3.  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
  3 in total

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