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Tandem aza-Michael addition-vinylogous aldol condensation: synthesis of N-bridged pyridine fused quinolones.
Gummidi, Lalitha; Muddassar, Altaf; Sharma, Gangavaram V M; Murugesh, V; Suresh, Surisetti.
Afiliação
  • Gummidi L; Department of Organic Synthesis and Process Chemistry, CSIR-Indian Institute of Chemical Technology (CSIR-IICT), Hyderabad 500 007, India. murugeshprasad@gmail.com.
  • Muddassar A; Department of Organic Synthesis and Process Chemistry, CSIR-Indian Institute of Chemical Technology (CSIR-IICT), Hyderabad 500 007, India. murugeshprasad@gmail.com.
  • Sharma GVM; Department of Organic Synthesis and Process Chemistry, CSIR-Indian Institute of Chemical Technology (CSIR-IICT), Hyderabad 500 007, India. murugeshprasad@gmail.com.
  • Murugesh V; Department of Organic Synthesis and Process Chemistry, CSIR-Indian Institute of Chemical Technology (CSIR-IICT), Hyderabad 500 007, India. murugeshprasad@gmail.com.
  • Suresh S; Academy of Scientific and Innovative Research (AcSIR), Ghaziabad 201 002, India.
Org Biomol Chem ; 20(4): 773-777, 2022 01 26.
Article em En | MEDLINE | ID: mdl-34991153
Herein, we present a tandem aza-Michael addition-vinylogous aldol condensation strategy for the synthesis of N-bridged pyridine fused quinolone derivatives from quinolones and ynones. The presented tandem transformation features the construction of C-N and CC bonds in a single operation, under transition metal-free conditions. The wide substrate scope and gram scale synthesis of pyridine fused quinolone derivatives expand the synthetic value of the presented protocol.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Org Biomol Chem Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Org Biomol Chem Ano de publicação: 2022 Tipo de documento: Article