Journal
SYNLETT
Volume 25, Issue 13, Pages 1879-1882Publisher
GEORG THIEME VERLAG KG
DOI: 10.1055/s-0034-1378323
Keywords
asymmetric catalysis; dynamic kinetic resolution; beta(2)-amino acids; hydrosilylation; Lewis base
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Funding
- National Natural Science Foundation of China [21172217, 20972155]
- National Basic Research Program of China (973 Program) [2010CB833301]
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A chiral Lewis base organocatalyzed asymmetric hydrosilylation of alpha-substituted beta-enamino esters is presented. The reactions proceeded through dynamic kinetic resolution to afford various enantioenriched beta(2)-amino esters with high yields (up to 98%) in moderate enantioselectivities (up to 77% ee).
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