Organo- f -Complexes for Efficient and Selective Hydroborations

Heng Liu*, Moris S. Eisen

*Corresponding author for this work

Research output: Contribution to journalReview articlepeer-review

4 Scopus citations

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.

Original languageEnglish
Pages (from-to)629-644
Number of pages16
JournalSynthesis
Volume52
Issue number5
DOIs
StatePublished - 3 Mar 2020
Externally publishedYes

Keywords

  • aldehyde
  • alkene
  • hydroboration
  • imine
  • ketone
  • organoactinide
  • organolanthanide
  • selective

Fingerprint

Dive into the research topics of 'Organo- f -Complexes for Efficient and Selective Hydroborations'. Together they form a unique fingerprint.

Cite this