Flexible routes to thiophenes

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

doi:10.1021/ol403310f

Flexible routes to thiophenes

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

Laboratoire de Synthèse Organique

Research output: Contribution to journal › Article › peer-review

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%).

Original language	English
Pages (from-to)	302-305
Number of pages	4
Journal	Organic Letters
Volume	16
Issue number	1
DOIs	https://doi.org/10.1021/ol403310f
Publication status	Published - 3 Jan 2014
Externally published	Yes

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title = "Flexible routes to thiophenes",

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\%).",

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journal = "Organic Letters",

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AU - Tétart, Thomas

AU - Zard, Samir Z.

PY - 2014/1/3

Y1 - 2014/1/3

N2 - 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%).

AB - 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%).

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DO - 10.1021/ol403310f

M3 - Article

AN - SCOPUS:84891781368

SN - 1523-7060

VL - 16

SP - 302

EP - 305

JO - Organic Letters

JF - Organic Letters

IS - 1

ER -

Flexible routes to thiophenes

Abstract

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