Abstract
The metal-catalyzed Meerwein-Ponndorf-Verley (MPV) reduction allows for the mild and sustainable reduction of aldehydes and ketones but has not found widespread application in organic synthesis due to the high catalyst loading often required to obtain satisfactory yields of the reduced product. We report here on the synthesis and structure of a sterically extremely overloaded siloxide-supported aluminum isopropoxide capable of catalytically reducing a wide range of aldehydes and ketones (52 examples) in excellent yields under mild conditions and with low catalyst loadings. The unseen activity of the developed catalyst system in MPV reductions is due to its unique monomeric nature and the neutral donor isopropanol weakly coordinating to the aluminum center. The present work implies that monomeric aluminum alkoxide catalysts may be attractive alternatives to transition-metal-based systems for the selective reduction of aldehydes and ketones to primary and secondary alcohols.
Original language | English |
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Pages (from-to) | 14959-14964 |
Number of pages | 6 |
Journal | Chemistry - A European Journal |
Volume | 20 |
Issue number | 46 |
DOIs | |
Publication status | Published - 10 Nov 2014 |
Keywords
- aldehydes
- aluminum
- ketones
- MPV reduction
- siloxide
- ASYMMETRIC TRANSFER HYDROGENATION
- CARBONYL-COMPOUNDS
- HIGHLY EFFICIENT
- IRON COMPLEXES
- PINCER LIGANDS
- ENANTIOSELECTIVE HYDROSILYLATION
- METAL-COMPLEXES
- PNNP LIGAND
- KETONES
- ALDEHYDES