Copper-catalyzed borylative cyclization of γ,δ-unsaturated aromatic oxime esters to (borylmethyl)pyrrolidines

文献情報

出版日 2020-09-17

DOI 10.1039/D0QO01064B

インパクトファクター 5.281

著者

Youcan Zhang

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要旨

An efficient copper-catalyzed aminoborylation of γ,δ-unsaturated aromatic oxime esters with bis(pinacolato)diboron has been developed. A variety of α-(borylmethyl)pyrrolidine derivatives were constructed in high yields under mild conditions. Notably, examples of converting the obtained aminoborylated product, including cycloaddition, oxidation, and coupling reactions, have been given as well.

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 borylative cyclization of γ,δ-unsaturated aromatic oxime esters to (borylmethyl)pyrrolidines

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