Visible Light-Promoted Oxidative Cross-Coupling of Alcohols to Esters

Author:

Dellisanti Andrea1,Chessa Elisa1,Porcheddu Andrea2ORCID,Carraro Massimo1ORCID,Pisano Luisa1,De Luca Lidia1ORCID,Gaspa Silvia1

Affiliation:

1. Dipartimento di Scienze Chimiche, Fisiche, Matematiche e Naturali, Università degli Sudi di Sassari, Via Vienna 2, 07100 Sassari, Italy

2. Dipartimento di Scienze Chimiche e Geologiche, Università degli Sudi di Cagliari, 09042 Monserrato, Italy

Abstract

Ester is one of the most significant functional groups in organic chemistry and is enclosed in several valued molecules. Usually, esters are prepared through the acid-catalyzed esterification reaction of carboxylic acids with alcohols, transesterification of esters with alcohols, or via activation of carboxylic acids followed by the addition of alcohols. However, these procedures typically imply the excess use of reactants and harsh reaction conditions. Visible light-mediated photoreactions have been disclosed to display a safe, sustainable, and accessible alternative to traditional methods, and to lead new reactivity modes in organic procedures. In this context, we propose a transition metal-based and organic-based photocatalyst-free synthesis of esters from alcohols induced by visible light. The methodology can be carried out using sunlight or artificial visible light as a solar simulator or a blue LED source.

Funder

Università degli Studi di Sassari within “Finanziamento straordinario una tantum per la ricerca 2020”

Publisher

MDPI AG

Subject

Chemistry (miscellaneous),Analytical Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Molecular Medicine,Drug Discovery,Pharmaceutical Science

Reference73 articles.

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