Issue 51, 2021

A modular olefination reaction between aldehydes and diborylsilylmethide lithium salts

Abstract

We describe the preparation of densely functionalised 1,1-silylborylated trisubstituted alkenes, via a boron-Wittig reaction, between LiC(Bpin)2(SiMe3) and aliphatic or aromatic aldehydes. The condensation of diborylsilylmethide lithium salts with α,β-unsaturated aldehydes provides a direct pathway to synthesize 1,1-silylborylated conjugated dienes and diynes.

Graphical abstract: A modular olefination reaction between aldehydes and diborylsilylmethide lithium salts

Supplementary files

Article information

Article type
Communication
Submitted
08 Apr 2021
Accepted
24 May 2021
First published
25 May 2021

Chem. Commun., 2021,57, 6300-6303

A modular olefination reaction between aldehydes and diborylsilylmethide lithium salts

O. Salvado and E. Fernández, Chem. Commun., 2021, 57, 6300 DOI: 10.1039/D1CC01882E

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