Silver(i)-catalyzed novel ipso-cycloaddition and retro-Friedel–Crafts reaction of ortho-hydroxyphenyl-substituted para-quinone methides

文献情報

出版日 2021-09-22

DOI 10.1039/D1QO01056E

インパクトファクター 5.281

著者

Caiqi Zhuo, Ran Song, Zhanxu Liu, Qirui Xiang, Daoshan Yang, Wen Si, Jian Lv

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要旨

The Lewis acid AgPF6 was found to catalyze novel [2 + 2] ipso-cycloaddition and retro-Friedel–Crafts reaction of ortho-hydroxyphenyl-substituted para-quinone methides in the presence of H2O (1 equiv.) effectively, affording the polysubstituted triarylmethanes in up to 97% yields.

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

Silver(i)-catalyzed novel ipso-cycloaddition and retro-Friedel–Crafts reaction of ortho-hydroxyphenyl-substituted para-quinone methides

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