Issue 34, 2019

Dimethyl sulfoxide as a “methylene” source: Ru(ii) photo-catalysed facile synthesis of acetals from alcohols

Abstract

Acetals are important molecules with versatile reactivity and uses. For the first time a simple photo-catalysed facile synthesis of formaldehyde acetals is documented herein upon the reaction of alcohols with dimethyl sulfoxide under very mild conditions in the presence of air. The reactions require only 1 mol% of RuII(bpy)3Cl2 photocatalyst under blue LED irradiation (λ = 445 nm) to give good to excellent yields of the corresponding acetal products. Here DMSO acts as a “methylene” source.

Graphical abstract: Dimethyl sulfoxide as a “methylene” source: Ru(ii) photo-catalysed facile synthesis of acetals from alcohols

Supplementary files

Article information

Article type
Letter
Submitted
01 Jul 2019
Accepted
02 Aug 2019
First published
05 Aug 2019

New J. Chem., 2019,43, 13334-13338

Dimethyl sulfoxide as a “methylene” source: Ru(II) photo-catalysed facile synthesis of acetals from alcohols

R. Talukdar, New J. Chem., 2019, 43, 13334 DOI: 10.1039/C9NJ03422F

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements