Synthesis of benzisoxazolines by the coupling of arynes with nitrones.

The Journal of Organic Chemistry
Chun LuRichard C Larock

Abstract

A variety of substituted benzisoxazolines have been synthesized by the [3 + 2] cycloaddition of nitrones and arynes. The reaction scope is broad, the reaction conditions are mild, and the process tolerates a variety of functional groups.

References

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Citations

Aug 7, 2012·Organic Letters·Sachin Suresh BhojgudeAkkattu T Biju
Jul 27, 2012·Organic Letters·Ranjeet A DhokaleSantosh B Mhaske
Mar 19, 2016·Journal of the American Chemical Society·Tejas K ShahNeil K Garg
Dec 17, 2015·Chemistry : a European Journal·Wei ZhangYan-Jun Xu
Jul 23, 2014·The Journal of Organic Chemistry·Emmanuel B Castillo-ContrerasGregory R Dake
Jan 10, 2018·Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan·Akira Takagi
Oct 24, 2015·Chemical Record : an Official Publication of the Chemical Society of Japan ... [et Al.]·Guanyinsheng Qiu, Jie Wu
Sep 19, 2019·Angewandte Chemie·Daniel B Werz, Akkattu T Biju
Nov 8, 2012·Organic & Biomolecular Chemistry·Anton V DubrovskiyRichard C Larock
Feb 19, 2021·Chemical Reviews·Jiarong ShiYang Li
Apr 15, 2021·The Journal of Organic Chemistry·Yuan-Ze XuXin-Yan Wu
Mar 2, 2017·The Journal of Organic Chemistry·Takashi IkawaShuji Akai
Sep 12, 2019·The Journal of Organic Chemistry·Avishek GuinAkkattu T Biju
Oct 5, 2018·Journal of the American Chemical Society·Dachuan QiuYang Li
Dec 15, 2021·The Journal of Organic Chemistry·Leonie O'SullivanDarren J Derksen

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