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A modular olefination reaction between aldehydes and diborylsilylmethide lithium salts
- 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