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Intramolecular Acylation of Unactivated Pyridines or Arenes via Multiple C-H Functionalizations: Synthesis of All Four Azafluorenones and Fluorenones.
Laha, Joydev K; Jethava, Krupal P; Patel, Sagarkumar; Patel, Ketul V.
Afiliação
  • Laha JK; Department of Pharmaceutical Technology (Process Chemistry), National Institute of Pharmaceutical Education and Research Sahibzada Ajit Singh Nagar, Punjab 160062, India.
  • Jethava KP; Department of Pharmaceutical Technology (Process Chemistry), National Institute of Pharmaceutical Education and Research Sahibzada Ajit Singh Nagar, Punjab 160062, India.
  • Patel S; Department of Pharmaceutical Technology (Process Chemistry), National Institute of Pharmaceutical Education and Research Sahibzada Ajit Singh Nagar, Punjab 160062, India.
  • Patel KV; Department of Pharmaceutical Technology (Process Chemistry), National Institute of Pharmaceutical Education and Research Sahibzada Ajit Singh Nagar, Punjab 160062, India.
J Org Chem ; 82(1): 76-85, 2017 01 06.
Article em En | MEDLINE | ID: mdl-27966934
ABSTRACT
An unprecedented intramolecular acylation of unactivated pyridines via multiple C(sp3/sp2)-H functionalizations of a methyl, hydroxymethyl, or aldehyde group has been developed providing a general access to all four azafluorenones. The application of this protocol is further demonstrated to the synthesis of azafluorenone related fused nitrogen heterocycles and fluorenones. In addition, design and synthesis of a novel fluorene based organic emitter for potential use in organic light emitting devices (OLEDs) is also reported.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: J Org Chem Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Índia

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: J Org Chem Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Índia