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Article Dans Une Revue Organic Letters Année : 2016

TiCl4-Mediated Preparation of Thiophthalide Derivatives via Formal Thio-Passerini Reactions

Résumé

By the formal extension of the Passerini reaction to thiocarbonyl derivatives, the straightforward preparation of thiophthalides is disclosed. This method involves the intermediate formation of a sulfanyl-phthalide and a titanium tetrachloride mediated isocyanide insertion reaction. When tent-butyl thiol is used, thanks to the deprotection of the tert-butyl group, a thiophthalide resulting from a 1,5-Mumm rearrangement is isolated. Owing to the multifaceted activity of TiCl4, all steps may conveniently be performed in one pot, starting directly from 2-formylbenzoic acids, tert-butyl thiol, and various isocyanides.

Domaines

Chimie organique
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Dates et versions

hal-01456154 , version 1 (04-02-2017)

Identifiants

Citer

Sudipta Ponra,, Aude Nyadanu,, Laurent El Kaim, Laurence Grimaud, Maxime R. Vitale. TiCl4-Mediated Preparation of Thiophthalide Derivatives via Formal Thio-Passerini Reactions. Organic Letters, 2016, 18 (16), pp.4060-4063. ⟨10.1021/acs.orglett.6b01937⟩. ⟨hal-01456154⟩
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