Abstract
A new heteroleptic cationic copper(I) complex bearing two N-heterocyclic carbene (NHC) ligands has been prepared. In situ, a Cu-O bond can be generated which enables the complex to catalytically activate H (2) . The resulting complex shows activity in catalytic chemo- and stereoselective alkyne semihydrogenations as well as conjugate reductions of enones.
Original language | English |
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Pages (from-to) | 783-786 |
Number of pages | 4 |
Journal | Synlett |
Volume | 30 |
Issue number | 7 |
DOIs | |
Publication status | Published - Apr-2019 |
Keywords
- copper
- NHC ligands
- hydrogenation
- homogeneous catalysis
- alkynes
- enones
- NHC LIGANDS
- MOLECULAR-HYDROGEN
- HYDROSILYLATION
- SEMIHYDROGENATION
- ACTIVATION
- MECHANISM
- HYDRIDES