Bifunctional organocatalyst for methanolytic desymmetrization of cyclic anhydrides: increasing enantioselectivity by catalyst dilution.
Bifunctional organocatalyst for methanolytic desymmetrization of cyclic anhydrides: increasing enantioselectivity by catalyst dilution. Research Abstract Details
Highly enantioselective methanolysis of meso-cyclic anhydride was achieved with bifunctional organocatalyst containing a quinine-thiourea moiety; unusual concentration, temperature and solvent effects on the enantioselectivity can be explained in terms of a mechanism involving monomer-dimer equilibration of the catalyst.
Bifunctional organocatalyst for methanolytic desymmetrization of cyclic anhydrides: increasing enantioselectivity by catalyst dilution. Publishing Authors By Initials
Bifunctional organocatalyst for methanolytic desymmetrization of cyclic anhydrides: increasing enantioselectivity by catalyst dilution. Journal Published:
PUBLICATION TYPE: Journal Article
Journal: Chemical communications (Cambridge, England)
VOLUME:
Page Numbers: 1208-10
Journal Abbreviation: Chem. Commun. (Camb.)
ISSN: 1359-7345
DAY: 6
MONTH: 02
YEAR: 2008
Bifunctional organocatalyst for methanolytic desymmetrization of cyclic anhydrides: increasing enantioselectivity by catalyst dilution. Information
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LANGUAGE: eng
NlmUniqueID: 9610838
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Grant and Affiliation Information for Bifunctional organocatalyst for methanolytic desymmetrization of cyclic anhydrides: increasing enantioselectivity by catalyst dilution.
AFFILIATION: Department of Chemistry, Sungkyunkwan University, 300 Cheoncheon, Jangan, Suwon, Gyeonggi, 440-746 Korea. s1673@skku.edu.
Country: England
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MEDLINETA: Chem Commun (Camb)
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