Literature DB >> 16118869

Highly selective palladium-catalyzed Heck reactions of aryl bromides with cycloalkenes.

C G Hartung1, K Köhler, M Beller.   

Abstract

[reaction: see text] The influence of palladium catalysts and reaction conditions on the selectivity of Heck reactions of aryl bromides with cyclohexene and cyclopentene has been investigated. It is shown that the addition of DMSO as a cosolvent leads to improved selectivities of nonconjugated aryl olefins. On the other hand, high selectivities for conjugated arylcyclopentenes have been obtained with the catalytic system DMA/Na2CO3/Pd2(dba)3 x dba/PCy3.

Entities:  

Year:  1999        PMID: 16118869     DOI: 10.1021/ol9901063

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


  2 in total

1.  Enantioselective Heck-Matsuda Arylations through Chiral Anion Phase-Transfer of Aryl Diazonium Salts.

Authors:  Carolina M Avila; Jigar S Patel; Yernaidu Reddi; Masato Saito; Hosea M Nelson; Hunter P Shunatona; Matthew S Sigman; Raghavan B Sunoj; F Dean Toste
Journal:  Angew Chem Int Ed Engl       Date:  2017-04-18       Impact factor: 15.336

2.  Selective Heck arylation of cyclohexene with homogeneous and heterogeneous palladium catalysts.

Authors:  Ewa Mieczyńska; Anna M Trzeciak
Journal:  Molecules       Date:  2010-03-25       Impact factor: 4.411

  2 in total

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