Literature DB >> 17523657

Ethynyl ketene-S,S-acetals: the highly reactive electron-rich dienophiles and applications in the synthesis of 4-functionalized quinolines via a one-pot three-component reaction.

Yu-Long Zhao1, Wei Zhang, Shuang Wang, Qun Liu.   

Abstract

An efficient synthetic method for 4-functionalized quinoline derivatives, 4-((1,3-dithian-2-ylidene)methyl)quinolines, has been developed. Mediated by trifluoromethanesulfonic acid, ethynyl ketene-S,S-acetals can react in a one-pot procedure with various arylamines and aldehydes under mild conditions to give the corresponding quinoline derivatives in good to high yields via a consecutive arylimine formation, regiospecific aza-Diels-Alder (Povarov) reaction, and reductive amination.

Entities:  

Year:  2007        PMID: 17523657     DOI: 10.1021/jo070069q

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


  3 in total

1.  Facile Synthesis and Photophysical Characterization of New Quinoline Dyes.

Authors:  Giovanny Carvalho Dos Santos; Aloisio de Andrade Bartolomeu; Valdecir Farias Ximenes; Luiz Carlos da Silva-Filho
Journal:  J Fluoresc       Date:  2016-10-27       Impact factor: 2.217

2.  One-pot phosphine-catalyzed syntheses of quinolines.

Authors:  San Khong; Ohyun Kwon
Journal:  J Org Chem       Date:  2012-09-06       Impact factor: 4.354

3.  Solvent-free and room temperature synthesis of 3-arylquinolines from different anilines and styrene oxide in the presence of Al2O3/MeSO3H.

Authors:  Hashem Sharghi; Mahdi Aberi; Mohsen Khataminejad; Pezhman Shiri
Journal:  Beilstein J Org Chem       Date:  2017-09-20       Impact factor: 2.883

  3 in total

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