Issue 29, 2024

Silylene acetals from cheap reagents: synthesis and regioselective opening

Abstract

In this communication, a practical method for using cheap and easily available silylene chlorides for diol protection is presented. The method is based on activation of the reagents using Finkelstein-like conditions. Silylene acetals of carbohydrates are synthesized, and it is furthermore shown how these can be regioselectively opened using Grignard reagents.

Graphical abstract: Silylene acetals from cheap reagents: synthesis and regioselective opening

Supplementary files

Article information

Article type
Paper
Submitted
03 May 2024
Accepted
02 Jul 2024
First published
03 Jul 2024

Org. Biomol. Chem., 2024,22, 5977-5981

Silylene acetals from cheap reagents: synthesis and regioselective opening

M. L. Zimmermann, D. M. Feldballe and C. M. Pedersen, Org. Biomol. Chem., 2024, 22, 5977 DOI: 10.1039/D4OB00721B

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