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Lipase/palladium-catalyzed asymmetric transformations of ketoximes to optically active amines SCIE SCOPUS

Title
Lipase/palladium-catalyzed asymmetric transformations of ketoximes to optically active amines
Authors
Choi, YKKim, MJAhn, YKim, MJ
Date Issued
2001-12-13
Publisher
AMER CHEMICAL SOC
Abstract
[GRAPHICS] Prochiral ketoximes were asymmetrically transformed, to optically active amines in the acetylated forms by coupled lipase/palladium catalysis in the presence of an acyl donor under 1 atm of hydrogen.
Keywords
DYNAMIC KINETIC RESOLUTION; ENANTIOSELECTIVE HYDROGENATION; SECONDARY ALCOHOLS; OXIME ETHERS; IMINES; REDUCTION; RUTHENIUM; HYDROSILYLATION; PALLADIUM; LIPASE
URI
https://oasis.postech.ac.kr/handle/2014.oak/19277
DOI
10.1021/OL0168622
ISSN
1523-7060
Article Type
Article
Citation
ORGANIC LETTERS, vol. 3, no. 25, page. 4099 - 4101, 2001-12-13
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김만주KIM, MAHN JOO
Dept of Chemistry
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