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

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发布日期 2021-09-22

DOI 10.1039/D1QO01056E

影响因子 5.281

作者

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

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摘要

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.

期刊推荐

Accounts of Chemical Research

Cement and Concrete Research

Chemical & Pharmaceutical Bulletin

Journal of the American Chemical Society

AIAA Journal

Doklady Chemistry

Bulletin of the Chemical Society of Japan

Canadian Metallurgical Quarterly

Chemistry of Heterocyclic Compounds

Anti-Corrosion Methods and Materials

来源期刊

Organic Chemistry Frontiers

CiteScore: 7.8

自引率: 8.7%

年发文量: 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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来源期刊

Organic Chemistry Frontiers

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