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Bae, Han Yong
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Hydrogen bonding mediated enantioselective organocatalysis in brine: significant rate acceleration and enhanced stereoselectivity in enantioselective Michael addition reactions of 1,3-dicarbonyls to beta-nitroolefins

Author(s)
Bae, Han YongSome, SurajitOh, Joong SukLee, Yong SeopSong, Choong Eui
Issued Date
2011-09
DOI
10.1039/c1cc13637b
URI
https://scholarworks.unist.ac.kr/handle/201301/25861
Fulltext
https://pubs.rsc.org/en/Content/ArticleLanding/2011/CC/c1cc13637b#!divAbstract
Citation
CHEMICAL COMMUNICATIONS, v.47, no.34, pp.9621 - 9623
Abstract
Brine provides remarkable rate acceleration and a higher level of stereoselectivity over organic solvents, due to the hydrophobic hydration effect, in the enantioselective Michael addition reactions of 1,3-dicarbonyls to beta-nitroolefins using chiral H-donors as organocatalysts.
Publisher
ROYAL SOC CHEMISTRY
ISSN
1359-7345
Keyword
WATERDERIVATIVES

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