Literature DB >> 24069899

A direct method for oxidizing quinoxaline, tetraazaphenanthrene, and hexaazatriphenylene moieties using hypervalent λ3-iodinane compounds.

Ludovic Troian-Gautier1, Julien De Winter, Pascal Gerbaux, Cécile Moucheron.   

Abstract

An efficient oxidation reaction of various electron-poor quinoxaline-core-containing compounds, such as quinoxalines, 1,4,5,8-tetraazaphenanthrenes, and 1,4,5,8,9,12-hexaazatriphenylene, using [bis(trifluoroacetoxy)iodo]benzene is reported. These compounds are converted into the corresponding quinoxalinediones in good to high yields at room temperature using an acetonitrile/water solvent mixture. This unprecedented reaction should enable the synthesis of a wide variety of compounds useful in several fields of chemistry.

Entities:  

Year:  2013        PMID: 24069899     DOI: 10.1021/jo401872e

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


  2 in total

1.  A theoretical study on diastereoselective oxidative dearomatization by iodoxybenzoic acid.

Authors:  Vincent Tognetti; Agathe Boulangé; Philippe A Peixoto; Xavier Franck; Laurent Joubert
Journal:  J Mol Model       Date:  2014-07-20       Impact factor: 1.810

2.  A new hypervalent iodine(iii/v) oxidant and its application to the synthesis of 2H-azirines.

Authors:  Guangtao Zhang; Yuanxun Wang; Jun Xu; Jiyun Sun; Fengxia Sun; Yilin Zhang; Chenglin Zhang; Yunfei Du
Journal:  Chem Sci       Date:  2019-12-06       Impact factor: 9.825

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.