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Synthesis of Trifluoromethyl- and Ester Group-Substituted α-Carbolines via Iron-Catalyzed Tandem Cyclization Reaction.
Xu, Yumin; Chen, Xiaoqian; Gao, Yiqin; Yan, Zicong; Wan, Changfeng; Liu, Jin-Biao; Wang, Zhiyong.
Afiliação
  • Xu Y; College of Chemistry and Chemical Engineering and Key Laboratory of Functional Small Organic Molecule, Ministry of Education, Jiangxi Normal University, Nanchang 330022, China.
  • Chen X; College of Chemistry and Chemical Engineering and Key Laboratory of Functional Small Organic Molecule, Ministry of Education, Jiangxi Normal University, Nanchang 330022, China.
  • Gao Y; College of Chemistry and Chemical Engineering and Key Laboratory of Functional Small Organic Molecule, Ministry of Education, Jiangxi Normal University, Nanchang 330022, China.
  • Yan Z; Department of Chemistry, University of Science and Technology of China, Hefei 230026, China.
  • Wan C; College of Chemistry and Chemical Engineering and Key Laboratory of Functional Small Organic Molecule, Ministry of Education, Jiangxi Normal University, Nanchang 330022, China.
  • Liu JB; College of Chemistry and Chemical Engineering and Key Laboratory of Functional Small Organic Molecule, Ministry of Education, Jiangxi Normal University, Nanchang 330022, China.
  • Wang Z; School of Metallurgy and Chemical Engineering, Jiangxi University of Science and Technology, Ganzhou 341000, China.
J Org Chem ; 85(6): 4354-4364, 2020 03 20.
Article em En | MEDLINE | ID: mdl-32090568
ABSTRACT
An efficient approach to prepare trifluoromethyl-α-carbolines and ester group-substituted α-carbolines via the tandem cyclization reaction of 2-(2-aminophenyl)acetonitriles and trifluoromethyl 1,3-diones or ß,γ-unsaturated α-ketoesters was reported. The transformation proceeded smoothly in the presence of catalytic environmental-benign iron salts, which are used to prepare the desired products in moderate to good yields.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2020 Tipo de documento: Article