Abstract
A new catalytic system based on a ZnII NHC precursor has been developed for the cross-coupling reaction of alkyl halides with diboron reagents, which represents a novel use of a Group XII catalyst for C-X borylation. This approach gives borylations of unactivated primary, secondary, and tertiary alkyl halides at room temperature to furnish alkyl boronates, with good functional-group compatibility, under mild conditions. Preliminary mechanistic investigations demonstrated that this borylation reaction seems to involve one-electron processes.
Original language | English |
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Pages (from-to) | 1799-1803 |
Number of pages | 5 |
Journal | Angewandte Chemie International Edition |
Volume | 53 |
Issue number | 7 |
Early online date | 13 Jan 2014 |
DOIs | |
Publication status | Published - 10 Feb 2014 |
Keywords
- boronate esters
- Cross-coupling
- homogeneous catalysis
- N-heterocyclic carbenes
- Suzuki-Miyaura