Issue 22, 1998

Heterogeneous asymmetric aminohydroxylation of alkenes using a silica gel-supported bis-cinchona alkaloid

Abstract

Excellent enantioselectivities of up to >99% ee have been achieved in the heterogeneous asymmetric aminohydroxylation of trans-cinnamate derivatives using silica gel-supported (QN)2PHAL [SGS-(QN)2PHAL 1]; the dark brown 1·Os complex, recovered by simple filtration after reaction, could be reused without any loss of enantioselectivity.

Article information

Article type
Paper

Chem. Commun., 1998, 2435-2436

Heterogeneous asymmetric aminohydroxylation of alkenes using a silica gel-supported bis-cinchona alkaloid

C. Eui Song, C. Rim Oh, S. Woo Lee, S. Lee, L. Canali and D. C. Sherrington, Chem. Commun., 1998, 2435 DOI: 10.1039/A806959J

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