Copper-catalyzed nitrene transfer/cyclization cascade to synthesize 3a-nitrogenous furoindolines and pyrroloindolines

文献情報

出版日 2019-10-28

DOI 10.1039/C9QO01124B

インパクトファクター 5.281

著者

Guang-Yi Zhang, Yi Peng, Jing Xue, Yan-Hui Fan, Qing-Hai Deng

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要旨

An efficient copper-catalyzed nitrene transfer/cyclization of tryptophols and tryptamines was successfully developed. A series of 3a-nitrogenous indole alkaloids were obtained in good to excellent yields (up to 99%) using aryl azides as the nitrogen source.

掲載誌

Organic Chemistry Frontiers

CiteScore: 7.8

自己引用率: 8.7%

年間論文数: 724

Organic Chemistry Frontiers publishes high-quality research from across organic chemistry. Emphases are placed on studies that make significant contributions to the field of organic chemistry by reporting either new or significantly improved protocols or methodologies. Topics include, but are not limited to the following: Organic synthesis Development of synthetic methodologies Catalysis Natural products Functional organic materials Supramolecular and macromolecular chemistry Physical and computational organic chemistry

Copper-catalyzed nitrene transfer/cyclization cascade to synthesize 3a-nitrogenous furoindolines and pyrroloindolines

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