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A Mild Two-Step Synthesis of Structurally Valuable Indole-Fused Derivatives.
Chen, Shanping; Xia, Yi; Jin, Shikai; Lei, Hanwen; You, Kuiyi; Deng, Guo-Jun.
Afiliação
  • Chen S; Key Laboratory for Green Organic Synthesis and Application of Hunan Province, Key Laboratory of Environmentally Friendly Chemistry and Application of Ministry of Education, College of Chemistry, Xiangtan University, Xiangtan 411105, China.
  • Xia Y; School of Chemical Engineering, Xiangtan University, Xiangtan 411105, China.
  • Jin S; Key Laboratory for Green Organic Synthesis and Application of Hunan Province, Key Laboratory of Environmentally Friendly Chemistry and Application of Ministry of Education, College of Chemistry, Xiangtan University, Xiangtan 411105, China.
  • Lei H; Key Laboratory for Green Organic Synthesis and Application of Hunan Province, Key Laboratory of Environmentally Friendly Chemistry and Application of Ministry of Education, College of Chemistry, Xiangtan University, Xiangtan 411105, China.
  • You K; Key Laboratory for Green Organic Synthesis and Application of Hunan Province, Key Laboratory of Environmentally Friendly Chemistry and Application of Ministry of Education, College of Chemistry, Xiangtan University, Xiangtan 411105, China.
  • Deng GJ; School of Chemical Engineering, Xiangtan University, Xiangtan 411105, China.
J Org Chem ; 87(5): 3212-3222, 2022 03 04.
Article em En | MEDLINE | ID: mdl-35152695
ABSTRACT
A mild two-step synthetic approach for the preparation of structurally valuable indolo[3',2'4,5]pyrrolo[3,2,1-kl]phenothiazines has been developed. In this work, cyclohexanone was used as the key bridge to connect the indole and phenothiazine frameworks to construct a structurally valuable indole-fused derivative. The present protocol achieved the cascade construction of multiple C-hetero bonds, affording a convenient approach access to hexacyclic-fused system that contained both indole and phenothiazine, two privileged skeletons.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Indóis Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Indóis Idioma: En Ano de publicação: 2022 Tipo de documento: Article