Synthetic approach to skeletally diverse nitrogen heterocycles from dicyano-2-methylenebut-3-enoates

文献情報

出版日 2019-05-08

DOI 10.1039/C9QO00509A

インパクトファクター 5.281

著者

Wen-Lin Zou, Qing-Zhu Li, Xin Feng, Zhi-Qiang Jia, Yue Liu

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要旨

The [2 + 1], formal-[4 + 1] and [5 + 1] annulations of electron-deficient dienes with ambiphilic nitrogen reagents were developed on the basis of a similar vinylogous aza-Michael addition. These synthetic approaches enable the divergent synthesis of several interesting heterocyclic skeletons, such as vinylaziridines, pyrroline and 2-aminopyridines, from easily accessible starting materials under mild conditions.

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

Synthetic approach to skeletally diverse nitrogen heterocycles from dicyano-2-methylenebut-3-enoates

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