Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/138240
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dc.contributor.authorLiu, Binen_US
dc.contributor.authorYan, Jiekuanen_US
dc.contributor.authorHuang, Ruoyanen_US
dc.contributor.authorWang, Weihongen_US
dc.contributor.authorJin, Zhichaoen_US
dc.contributor.authorZanoni, Giuseppeen_US
dc.contributor.authorZheng, Pengchengen_US
dc.contributor.authorYang, Songen_US
dc.contributor.authorChi, Robin Yongguien_US
dc.date.accessioned2020-04-29T08:12:39Z-
dc.date.available2020-04-29T08:12:39Z-
dc.date.issued2018-
dc.identifier.citationLiu, B., Yan, K., Huang, R., Wang, W., Jin, Z, Zanoni, G., . . ., Chi, R. Y. (2018). Kinetic resolution of 1,2-diols via NHC-catalyzed site-selective esterification. Organic letters, 20(12), 3447-3450. doi:10.1021/acs.orglett.8b01029en_US
dc.identifier.issn1523-7052en_US
dc.identifier.urihttps://hdl.handle.net/10356/138240-
dc.description.abstractA kinetic resolution of 1,2-diols bearing both a secondary and a primary alcohol motif through an N-heterocyclic carbene-catalyzed oxidative acylation reaction has been developed. A site- and enantioselective esterification reaction is involved for this process. Both the monoacylated diols obtained and the remaining enantioenriched 1,2-diols are versatile building blocks for the preparation of functional molecules with proven biological activities.en_US
dc.description.sponsorshipNRF (Natl Research Foundation, S’pore)en_US
dc.description.sponsorshipASTAR (Agency for Sci., Tech. and Research, S’pore)en_US
dc.description.sponsorshipMOE (Min. of Education, S’pore)en_US
dc.language.isoenen_US
dc.relation.ispartofOrganic lettersen_US
dc.rights© 2018 American Chemical Society. All rights reserved. This paper was published in Organic letters and is made available with permission of American Chemical Society.en_US
dc.subjectScience::Chemistry::Organic chemistryen_US
dc.titleKinetic resolution of 1,2-diols via NHC-catalyzed site-selective esterificationen_US
dc.typeJournal Articleen
dc.contributor.schoolSchool of Physical and Mathematical Sciencesen_US
dc.identifier.doi10.1021/acs.orglett.8b01029-
dc.description.versionAccepted versionen_US
dc.identifier.pmid29863883-
dc.identifier.scopus2-s2.0-85048787588-
dc.identifier.issue12en_US
dc.identifier.volume20en_US
dc.identifier.spage3447en_US
dc.identifier.epage3450en_US
dc.subject.keywordsEnantioselectiveen_US
dc.subject.keywordsEsterificationen_US
item.grantfulltextopen-
item.fulltextWith Fulltext-
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