Rhodium(III)-Catalyzed [4+3] Annulation of <i>N</i>-Aryl-pyrazolidinones and Propargylic Acetates: Access to Benzo[<i>c</i>][1,2]diazepines.

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作者： Tingfang,Li ^[1] ; Zi,Yang ^[1] ; Zhenyu,Song ^[1] ; Remi,Chauvin ^[1] ; Xiuling,Cui ^[2]

作者单位： Engineering Research Centre of Molecular Medicine of Ministry of Education, Key Laboratory of Fujian Molecular Medicine, Key Laboratory of Precision Medicine and Molecular Diagnosis of Fujian Universities, Key Laboratory of Xiamen Marine and Gene Drugs, School of Biomedical Sciences, Huaqiao University, Xiamen 361021, P. R. China. ^[1] LCC-CNRS, Université de Toulouse, UPS, 205 route de Narbonne, 31077 Toulouse, France. ^[2]

DOI 10.1021/acs.orglett.0c01139

PMID 32400162

发布时间 2020-09-23

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2020年22卷11期

4078-4082页

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Rhodium(III)-Catalyzed [4+3] Annulation of <i>N</i>-Aryl-pyrazolidinones and Propargylic Acetates: Access to Benzo[<i>c</i>][1,2]diazepines.

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Rhodium(III)-Catalyzed [4+3] Annulation of <i>N</i>-Aryl-pyrazolidinones and Propargylic Acetates: Access to Benzo[<i>c</i>][1,2]diazepines.

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