Literature DB >> 29154548

Synthesis of 4-Isoxazolines via Visible-Light Photoredox-Catalyzed [3 + 2] Cycloaddition of Oxaziridines with Alkynes.

Gwang Seok Jang1, Junggeun Lee1, Jungseok Seo1, Sang Kook Woo1.   

Abstract

A method for [3 + 2] cycloaddition of oxaziridines with alkynes to form 4-isoxazolines via visible-light photoredox catalysis is described. This method is a greener, atom-economical reaction that tolerates various functional groups and provides good to excellent yield. Moreover, the cyclization products can be conveniently converted into tetrasubstituted allylic alcohols and enamines. A mechanistic study suggests that the reaction involves photoredox-catalyzed in situ generation of a nitrone from the oxaziridine by SET.

Entities:  

Year:  2017        PMID: 29154548     DOI: 10.1021/acs.orglett.7b03369

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  2 in total

1.  Synthesis of spirocyclic Δ4-isoxazolines via [3 + 2] cycloaddition of indanone-derived ketonitrones with alkynes.

Authors:  Yilin Liu; Jiaxue Liu; Yan-Yun Liu; Boxiao Tang; Hongwei Lin; Yuanxiang Li; Lin Zhang
Journal:  RSC Adv       Date:  2021-09-13       Impact factor: 3.361

Review 2.  Recent Advances in the Catalytic Asymmetric Reactions of Oxaziridines.

Authors:  Qiao Ren; Wen Yang; Yunfei Lan; Xurong Qin; Youzhou He; Lujiang Yuan
Journal:  Molecules       Date:  2018-10-16       Impact factor: 4.411

  2 in total

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