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DOI: 10.1055/s-0041-1738071
Transformations of Main-Group Organometallics Induced by Transition Metals
Abstract
The oxidative dehydrometallation of silyl or boron enolates is induced by palladium(II) catalyst to result in the versatile introduction of α,β-unsaturated carbon–carbon double bonds via palladium enolates. Selective oxidative cross- and homo-coupling reactions of silyl or boron enolates induced by vanadium(V) oxidant provide a selective synthetic method for accessing 1,4-dicarbonyl compounds in a nucleophile-nucleophile coupling mode. The ligand coupling reaction of main-group organometallic compounds induced by vanadium(V) oxidant provides a unique method for intramolecular carbon–carbon bond formation of nucleophiles. The last two reactions are a complementary strategy for the nucleophile-electrophile coupling reaction. The dehydrometallation and coupling reactions probably proceed through two- and one-electron oxidation processes, respectively.
1 Introduction
2 Palladium-Catalyzed Dehydrometallation
3 Homo- and Cross-Coupling of Main-Group Organometallic Compounds
4 Oxidative Ligand Coupling of Main-Group Organometallic Compounds
5 Conclusion
Key words
dehydrosilylation - boron enolates - palladium enolates - dehydroboration - α,β-carbon–carbon double bonds - 1,4-diketones - ligand coupling - main-group organometallicsPublication History
Received: 22 February 2022
Accepted after revision: 01 April 2022
Article published online:
10 May 2022
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