Literature DB >> 22410674

Nickel-catalyzed [4+2] cycloaddition for highly substituted arenes.

Hiroaki Horie1, Takuya Kurahashi, Seijiro Matsubara.   

Abstract

Nickel(0) catalyzed [4+2] cycloaddition of electron-deficient dienes to alkynes and subsequent aromatization gave highly substituted arenes. This formal inverse electron-demand Diels-Alder cycloaddition is attributed to the formation of a seven-membered nickelacycle from a diene and an alkyne. This journal is © The Royal Society of Chemistry 2012

Entities:  

Year:  2012        PMID: 22410674     DOI: 10.1039/c2cc30801k

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


  2 in total

1.  Mechanism, reactivity, and selectivity of nickel-catalyzed [4 + 4 + 2] cycloadditions of dienes and alkynes.

Authors:  Xin Hong; Dane Holte; Daniel C G Götz; Phil S Baran; K N Houk
Journal:  J Org Chem       Date:  2014-11-07       Impact factor: 4.354

2.  Ligand-field transition-induced C-S bond formation from nickelacycles.

Authors:  Jeongcheol Shin; Jiseon Lee; Jong-Min Suh; Kiyoung Park
Journal:  Chem Sci       Date:  2021-11-10       Impact factor: 9.825

  2 in total

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