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Lipase-catalyzed kinetic resolution of 3-phenyloxazolidin-2-one derivatives: Cascade O- and N-alkoxycarbonylations
KTH, School of Chemical Science and Engineering (CHE), Chemistry.
KTH, School of Chemical Science and Engineering (CHE), Chemistry.
KTH, School of Chemical Science and Engineering (CHE), Chemistry.
KTH, School of Chemical Science and Engineering (CHE), Chemistry, Organic Chemistry.ORCID iD: 0000-0003-1121-4007
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2016 (English)In: Catalysis communications, ISSN 1566-7367, E-ISSN 1873-3905, Vol. 82, 11-15 p.Article in journal (Refereed) Published
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Abstract [en]

A lipase-catalyzed, cascade kinetic resolution protocol has been established for the synthesis of 3-phenyloxazolidin-2-one derivatives with up to excellent enantioselectivities (95% ee). Candida antarctica lipase B showed high catalytic activity and stereoselectivity in sequential O- and N-alkoxycarbonylation processes.

Place, publisher, year, edition, pages
Elsevier, 2016. Vol. 82, 11-15 p.
Keyword [en]
Asymmetric, synthesis, Candida antarctica lipase B, Cascade alkoxycarbonylation, Kinetic resolution, Oxazolidinone, Candida, Catalysis, Catalyst activity, Isomers, Yeast, Alkoxycarbonylation, Lipase-catalyzed, Oxazolidinones, Kinetics
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Chemical Sciences
Identifiers
URN: urn:nbn:se:kth:diva-186907DOI: 10.1016/j.catcom.2016.04.009ISI: 000377735500003Scopus ID: 2-s2.0-84964547460OAI: oai:DiVA.org:kth-186907DiVA: diva2:931187
Note

Funding Details: KTH, China Scholarship Council

QC 20160526

Available from: 2016-05-26 Created: 2016-05-16 Last updated: 2016-07-15Bibliographically approved

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