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A modular olefination reaction between aldehydes and diborylsilylmethide lithium salts

Authors :
Universitat Rovira i Virgili
Salvado, Oriol; Fernandez, Elena
Universitat Rovira i Virgili
Salvado, Oriol; Fernandez, Elena
Source :
Chemical Communications; 10.1039/d1cc01882e; Chemical Communications. 57 (51): 6300-6303
Publication Year :
2021

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 alpha,beta-unsaturated aldehydes provides a direct pathway to synthesize 1,1-silylborylated conjugated dienes and diynes.

Details

Database :
OAIster
Journal :
Chemical Communications; 10.1039/d1cc01882e; Chemical Communications. 57 (51): 6300-6303
Publication Type :
Electronic Resource
Accession number :
edsoai.on1443573925
Document Type :
Electronic Resource