Literature DB >> 23692460

Oxidative radical skeletal rearrangement induced by molecular oxygen: synthesis of quinazolinones.

Yi-Feng Wang1, Feng-Lian Zhang, Shunsuke Chiba.   

Abstract

Oxidative skeletal rearrangement of 5-aryl-4,5-dihydro-1,2,4-oxadiazoles into quinazolinones is induced by molecular oxygen (under a dry air atmosphere) that likely proceeds via transient iminyl radical species. Concise syntheses of biologically active quinazolinone derivatives were demonstrated using the present strategy.

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Year:  2013        PMID: 23692460     DOI: 10.1021/ol4011745

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


  3 in total

1.  Rapid access to the heterocyclic core of the calyciphylline A and daphnicyclidin A-type Daphniphyllum alkaloids via tandem cyclization of a neutral aminyl radical.

Authors:  Ahmad A Ibrahim; Alexander N Golonka; Alberto M Lopez; Jennifer L Stockdill
Journal:  Org Lett       Date:  2014-02-07       Impact factor: 6.005

Review 2.  Oxime radicals: generation, properties and application in organic synthesis.

Authors:  Igor B Krylov; Stanislav A Paveliev; Alexander S Budnikov; Alexander O Terent'ev
Journal:  Beilstein J Org Chem       Date:  2020-06-05       Impact factor: 2.883

3.  ortho-Naphthoquinone-catalyzed aerobic oxidation of amines to fused pyrimidin-4(3H)-ones: a convergent synthetic route to bouchardatine and sildenafil.

Authors:  Kyeongha Kim; Hun Young Kim; Kyungsoo Oh
Journal:  RSC Adv       Date:  2020-08-21       Impact factor: 4.036

  3 in total

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