Ph3P-mediated decarboxylative ring-opening of maleic anhydride by thiolic compounds: formation of two carbon–sulfur bonds

N. Nowrouzi; M. Abbasi; Z. Zellifard

doi:10.1039/D3RA00294B

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Ph₃P-mediated decarboxylative ring-opening of maleic anhydride by thiolic compounds: formation of two carbon–sulfur bonds†

N. Nowrouzi,

*^a M. Abbasi

^a and Z. Zellifard^a

Author affiliations

* Corresponding authors

^a Department of Chemistry, Faculty of Nano and Bio Science and Technology, Persian Gulf University, Bushehr, Iran
E-mail: nowrouzi@pgu.ac.ir
Fax: +98-77-33441494
Tel: +98-77-31222341

Abstract

In this study, a simple and efficient method for the formation of carbon–sulfur bonds is described. In this process, ring opening of maleic anhydride by thiols or disulfides and triphenylphosphine led to the formation of sulfide products via formation of two carbon-sulfur bonds.

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Article information

DOI: https://doi.org/10.1039/D3RA00294B
Article type: Paper
Submitted: 15 Jan 2023
Accepted: 13 Mar 2023
First published: 20 Mar 2023
This article is Open Access

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RSC Adv., 2023,13, 9242-9246

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Ph₃P-mediated decarboxylative ring-opening of maleic anhydride by thiolic compounds: formation of two carbon–sulfur bonds

N. Nowrouzi, M. Abbasi and Z. Zellifard, RSC Adv., 2023, 13, 9242 DOI: 10.1039/D3RA00294B

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

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