Flexible Routes to Thiophenes

descriptionPublicationkeyboard_double_arrow_right Article 03 Dec 2013 France English Publisher:American Chemical Society (ACS)Journal:Organic Letters, volume 16, pages 302-305 (issn: 1523-7060, eissn: 1523-7052,

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Authors: Jullien, Hélène; Quiclet-Sire, Béatrice; Tétart, Thomas; Zard, Samir, Z.;

doi: 10.1021/ol403310f

pmid: 24299213

Flexible Routes to Thiophenes

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Abstract

Three convergent routes to thiophenes are described, hinging on the radical addition of α-xanthyl ketones to ethyl vinyl sulfide or to vinyl pivalate. The latter route ultimately proved to be the most versatile and efficient (61-94%).

Country

France

Related Organizations

École Polytechnique
France
Laboratory of Organic Synthesis
France

Keywords

[CHIM.ORGA]Chemical Sciences/Organic chemistry

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