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Synthesis of Isoquinolone, 1,2-Benzothiazine, and Naphtho[1',2':4,5]imidazo[1,2-a]pyridine Derivatives via Rhodium(III)-Catalyzed (4 + 2) Annulation.
Zhu, Yueyue; Dai, Rupeng; Huang, Chaoqun; Zhou, Wang; Zhang, Xiaoyuan; Yang, Kundi; Wen, Hongmei; Li, Wei; Liu, Jian.
Afiliação
  • Zhu Y; School of Pharmacy, Nanjing University of Chinese Medicine, Nanjing 210023, China.
  • Dai R; School of Pharmacy, Nanjing University of Chinese Medicine, Nanjing 210023, China.
  • Huang C; School of Pharmacy, Nanjing University of Chinese Medicine, Nanjing 210023, China.
  • Zhou W; School of Pharmacy, Nanjing University of Chinese Medicine, Nanjing 210023, China.
  • Zhang X; School of Pharmacy, Nanjing University of Chinese Medicine, Nanjing 210023, China.
  • Yang K; Department of Chemistry and Biochemistry, Miami University, Oxford, Ohio 45056, United States.
  • Wen H; School of Pharmacy, Nanjing University of Chinese Medicine, Nanjing 210023, China.
  • Li W; School of Pharmacy, Nanjing University of Chinese Medicine, Nanjing 210023, China.
  • Liu J; School of Pharmacy, Nanjing University of Chinese Medicine, Nanjing 210023, China.
J Org Chem ; 87(17): 11722-11734, 2022 09 02.
Article em En | MEDLINE | ID: mdl-35968716
ABSTRACT
In this study, we report a novel and efficient synthetic method to construct isoquinolone scaffold via the Rh(III)-catalyzed (4 + 2) annulation of benzamide with an unreported coupling reagent methyl 2-chloroacrylate. Accordingly, other valuable 1,2-benzothiazine and naphtho[1',2'4,5]imidazo[1,2-a]pyridine derivatives are also obtained through a similar synthetic protocol. Thus, our developed method is highlighted by high yield and reaction versatility.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Ródio Idioma: En Revista: J Org Chem Ano de publicação: 2022 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Ródio Idioma: En Revista: J Org Chem Ano de publicação: 2022 Tipo de documento: Article País de afiliação: China