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Achieving Nickel Catalyzed C-S Cross-Coupling under Mild Conditions Using Metal-Ligand Cooperativity.
Sikari, Rina; Sinha, Suman; Das, Siuli; Saha, Anannya; Chakraborty, Gargi; Mondal, Rakesh; Paul, Nanda D.
Affiliation
  • Sikari R; Department of Chemistry , Indian Institute of Engineering Science and Technology , Shibpur, Botanic Garden, Howrah 711103 , India.
  • Sinha S; Department of Chemistry , Indian Institute of Engineering Science and Technology , Shibpur, Botanic Garden, Howrah 711103 , India.
  • Das S; Department of Chemistry , Indian Institute of Engineering Science and Technology , Shibpur, Botanic Garden, Howrah 711103 , India.
  • Saha A; Department of Chemical Sciences , Indian Institute of Science Education and Research Kolkata , Mohanpur 741246 , India.
  • Chakraborty G; Department of Chemistry , Indian Institute of Engineering Science and Technology , Shibpur, Botanic Garden, Howrah 711103 , India.
  • Mondal R; Department of Chemistry , Indian Institute of Engineering Science and Technology , Shibpur, Botanic Garden, Howrah 711103 , India.
  • Paul ND; Department of Chemistry , Indian Institute of Engineering Science and Technology , Shibpur, Botanic Garden, Howrah 711103 , India.
J Org Chem ; 84(7): 4072-4085, 2019 Apr 05.
Article de En | MEDLINE | ID: mdl-30855958
ABSTRACT
A simple and efficient approach of C-S cross-coupling of a wide variety of (hetero)aryl thiols and (hetero)aryl halides under mild conditions, mostly at room temperature, catalyzed by well-defined singlet diradical Ni(II) catalysts bearing redox noninnocent ligands is reported. Taking advantage of ligand centered redox events, the high-energetic Ni(0)/Ni(II) or Ni(I)/Ni(III) redox steps were avoided in the catalytic cycle. The cooperative participation of both nickel and the coordinated ligands during oxidative addition/reductive elimination steps allowed us to perform the catalytic reactions under mild conditions.

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Langue: En Journal: J Org Chem Année: 2019 Type de document: Article Pays d'affiliation: Inde

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Langue: En Journal: J Org Chem Année: 2019 Type de document: Article Pays d'affiliation: Inde
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