Issue 15, 2019

Direct anodic (thio)acetalization of aldehydes with alcohols (thiols) under neutral conditions, and computational insight into the electrochemical formation of the acetals

Abstract

A versatile protocol for the production of acetals/thioacetals by means of direct electrochemical oxidation is developed here under neutral conditions, providing (thio)acetals with good functional group tolerance and a wide scope for both aldehydes and (thio)alcohols. DFT calculations reveal that direct electron transfer from the anode plays a key role in carbonyl activation during this acid free acetalization process.

Graphical abstract: Direct anodic (thio)acetalization of aldehydes with alcohols (thiols) under neutral conditions, and computational insight into the electrochemical formation of the acetals

Associated articles

Supplementary files

Article information

Article type
Communication
Submitted
10 May 2019
Accepted
02 Jul 2019
First published
03 Jul 2019

Green Chem., 2019,21, 4030-4034

Direct anodic (thio)acetalization of aldehydes with alcohols (thiols) under neutral conditions, and computational insight into the electrochemical formation of the acetals

C. Liu, Y. Shen, Z. Xiao, H. Yang, X. Han, K. Yuan and Y. Ding, Green Chem., 2019, 21, 4030 DOI: 10.1039/C9GC01554J

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