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Rh(III)-catalyzed oxidative [4+2] annulation of 2-arylquinoxalines and 2-aryl-2H-indazoles with allyl alcohols.
Nipate, Dhananjay S; Meena, Neha; Swami, Prakash N; Rangan, Krishnan; Kumar, Anil.
Afiliación
  • Nipate DS; Department of Chemistry, Birla Institute of Technology and Science Pilani, Pilani Campus, Rajasthan, 333031, India. anilkumar@pilani.bits-pilani.ac.in.
  • Meena N; Department of Chemistry, Birla Institute of Technology and Science Pilani, Pilani Campus, Rajasthan, 333031, India. anilkumar@pilani.bits-pilani.ac.in.
  • Swami PN; Department of Chemistry, Birla Institute of Technology and Science Pilani, Pilani Campus, Rajasthan, 333031, India. anilkumar@pilani.bits-pilani.ac.in.
  • Rangan K; Department of Chemistry, Birla Institute of Technology and Science Pilani, Hyderabad Campus, Telangana, 500078, India.
  • Kumar A; Department of Chemistry, Birla Institute of Technology and Science Pilani, Pilani Campus, Rajasthan, 333031, India. anilkumar@pilani.bits-pilani.ac.in.
Chem Commun (Camb) ; 60(3): 344-347, 2024 Jan 02.
Article en En | MEDLINE | ID: mdl-38078491
ABSTRACT
Synthesis of functionalized benzo[a]phenazines and indazolo[2,3-a]quinolines has been developed through Rh(III)-catalyzed oxidative annulation of 2-arylquinoxalines and 2-aryl-2H-indazoles with allyl alcohols, respectively. The method features a broad substrate scope, excellent functional group tolerance, good to high yields of annulated products, and scaled-up synthesis capability. Based on a preliminary mechanistic investigation, a tentative mechanism of annulation reaction has been proposed.

Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: Chem Commun (Camb) Asunto de la revista: QUIMICA Año: 2024 Tipo del documento: Article País de afiliación: India

Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: Chem Commun (Camb) Asunto de la revista: QUIMICA Año: 2024 Tipo del documento: Article País de afiliación: India