Literature DB >> 28829132

Synthetic Access to Oxazolidin-4-ones via Elimination/[3+2] Cycloaddition Reaction.

Shengsheng Jiang1, Kai Li1, Jun Yan1, Kuangxi Shi1, Chengtao Zhao1, Limin Yang1, Guofu Zhong1.   

Abstract

Elimination/[3+2] cycloaddition reactions of simple enals and unprotected isatins with haloamides have been developed. This transformation provides rapid access to highly functionalized oxazolidin-4-ones that are represented in bioactive compounds.

Entities:  

Year:  2017        PMID： 28829132     DOI： 10.1021/acs.joc.7b00547

Source DB:  PubMed          Journal:  J Org Chem        ISSN： 0022-3263            Impact factor:   4.354


  3 in total

Review 1.  The Fascinating Chemistry of α-Haloamides.

Authors:  Anna Fantinati; Vinicio Zanirato; Paolo Marchetti; Claudio Trapella
Journal:  ChemistryOpen       Date:  2020-01-13       Impact factor: 2.911

2.  Imidazolidin-4-ones via (3+2) cycloadditions of aza-oxyallyl cations onto (E)-Narylideneanilines.

Authors:  Oznur Eyilcim; Sezin Issever; Nuket Ocal; Scott Gronert; Ihsan Erden
Journal:  Tetrahedron Lett       Date:  2018-09-05       Impact factor: 2.415

3.  Synthesis of 2-Aminoimidazolones and Imidazolones by (3 + 2) Annulation of Azaoxyallyl Cations.

Authors:  Maria C DiPoto; Jimmy Wu
Journal:  Org Lett       Date:  2018-01-10       Impact factor: 6.005
  3 in total

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