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Synthesis 2020; 52(05): 629-644
DOI: 10.1055/s-0039-1690762
DOI: 10.1055/s-0039-1690762
review
Organo-f-Complexes for Efficient and Selective Hydroborations
This work was supported by the Israel Science Foundation administered by the Israel Academy of Science and Humanities under Contract No. 184/18.Further Information
Publication History
Received: 17 November 2019
Accepted: 18 November 2019
Publication Date:
02 January 2020 (online)
Abstract
Organo-f-complexes catalyzing small molecule transformations have been a hot topic in the past few years. Compared to other transformations, the hydroboration of C=X (X = C, N, O) unsaturated bonds serves as an important strategy to prepare organoborane derivatives, which are important intermediates in organic synthesis. This review outlines recent advances in organolanthanide and organoactinide complexes promoting the hydroboration of C=X containing substrates. After a brief introduction, three types of hydroboration will be presented: alkene hydroboration, carbonyl hydroboration, and imine and nitrile hydroborations. The catalytic performance, mechanism, and kinetic studies are discussed in detail, aiming to emphasize the catalytic differences between the diverse organo-f-catalysts. Additionally, challenges and future directions of this field are also presented.
1 Introduction
2 Alkene Hydroboration
3 Carbonyl Hydroboration
4 Imine and Nitrile Hydroboration
5 Conclusions and Outlook
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