Synthesis of N-indolated amino acids or peptides from 2-alkynylanilines via a dearomatization process

文献情報

出版日 2021-10-07

DOI 10.1039/D1QO01257F

インパクトファクター 5.281

著者

Weilian Qiu, Weiyi Wang, Yin Liu, Renhua Fan

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要旨

A one-pot stepwise procedure for the synthesis of N-indolated amino acids or peptides from readily available 2-alkynylanilines was reported. The protocol involves the oxidative dearomatization of 2-alkynylanilines, the imino exchange with aliphatic amines, and subsequent cascade cyclization/nucleophilic addition/aromatization. The synthetic method might allow a rapid access to indolactam alkaloid derivatives.

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

Synthesis of N-indolated amino acids or peptides from 2-alkynylanilines via a dearomatization process

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