Abstract
In 2000, our group reported on the first examples of successful deprotonations of 4-substituted cyclohexanones, using simple magnesium amide base chem., with the com. available chiral amine (R)-(+)-N-benzyl-a-methylbenzylamine. Further applications to asym. deprotonation reactions with alternative chiral base species have now been developed. In particular, new supported C2-sym. magnesium amide bases have been established. In turn, novel sol. and insol. polymers have been applied to the asym. deprotonation reaction of prochiral ketones with superb selectivity (Scheme 1). Furthermore, a supported base recycling protocol has also been developed. [on SciFinder(R)]
Original language | Undefined/Unknown |
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Pages | ORGN-045 |
Publication status | Published - 2008 |
Event | Asymmetric Reactions and Syntheses - Pennsylvania, United States Duration: 17 Aug 2008 → … |
Conference
Conference | Asymmetric Reactions and Syntheses |
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Country/Territory | United States |
City | Pennsylvania |
Period | 17/08/08 → … |
Keywords
- chiral amines
- asymmetric Mg-amide base processes