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Ir-Catalyzed Intramolecular Transannulation/C(sp2)-H Amination of 1,2,3,4-Tetrazoles by Electrocyclization.
Das, Sandip Kumar; Roy, Satyajit; Khatua, Hillol; Chattopadhyay, Buddhadeb.
Afiliação
  • Das SK; Center of Bio-Medical Research, Division of Molecular Synthesis & Drug Discovery , SGPGIMS Campus , Raebareli Road , Lucknow 226014 , Uttar Pradesh , India.
  • Roy S; Center of Bio-Medical Research, Division of Molecular Synthesis & Drug Discovery , SGPGIMS Campus , Raebareli Road , Lucknow 226014 , Uttar Pradesh , India.
  • Khatua H; Center of Bio-Medical Research, Division of Molecular Synthesis & Drug Discovery , SGPGIMS Campus , Raebareli Road , Lucknow 226014 , Uttar Pradesh , India.
  • Chattopadhyay B; Center of Bio-Medical Research, Division of Molecular Synthesis & Drug Discovery , SGPGIMS Campus , Raebareli Road , Lucknow 226014 , Uttar Pradesh , India.
J Am Chem Soc ; 140(27): 8429-8433, 2018 07 11.
Article em En | MEDLINE | ID: mdl-29953229
ABSTRACT
An efficient strategy for the intramolecular denitrogenative transannulation/C(sp2)-H amination of 1,2,3,4-tetrazoles bearing C8-substituted arenes, heteroarenes, and alkenes is described. The process involves the generation of the metal-nitrene intermediate from tetrazole by the combination of [Cp*IrCl2]2 and AgSbF6. It has been shown that the reaction proceeds via an unprecedented electrocyclization process. The method has been successfully applied for the synthesis of a diverse array of α-carbolines and 7-azaindoles.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: J Am Chem Soc Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Índia

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: J Am Chem Soc Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Índia
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