Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/82679
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dc.contributor.authorDing, Feiqingen
dc.contributor.authorWilliam, Ronnyen
dc.contributor.authorKock, Si Minen
dc.contributor.authorLeow, Min Lien
dc.contributor.authorLiu, Xue-Weien
dc.date.accessioned2016-03-15T06:26:46Zen
dc.date.accessioned2019-12-06T15:00:14Z-
dc.date.available2016-03-15T06:26:46Zen
dc.date.available2019-12-06T15:00:14Z-
dc.date.issued2015en
dc.identifier.citationDing, F., William, R., Kock, S. M., Leow, M. L., & Liu, X.-W. (2015). A concise route to the highly-functionalized azetidine precursor: the enantioselective synthesis of penaresidin B. Chemical Communications, 51(22), 4639-4642.en
dc.identifier.issn1359-7345en
dc.identifier.urihttps://hdl.handle.net/10356/82679-
dc.description.abstractAn efficient and high-yielding synthesis of penaresidin B is disclosed herein. The concise 8-step synthesis of azetidine aldehyde was devised by incorporating our novel strategy for ready access to 3-amino-2,3-dideoxysugars via regio- and stereoselective tandem hydroamination/glycosylation of glycal as the key step.en
dc.description.sponsorshipMOE (Min. of Education, S’pore)en
dc.format.extent4 p.en
dc.language.isoenen
dc.relation.ispartofseriesChemical Communicationsen
dc.rightsThis article is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported Licence.en
dc.subjectazetidineen
dc.subjectglycosylationen
dc.titleA concise route to the highly-functionalized azetidine precursor: the enantioselective synthesis of penaresidin Ben
dc.typeJournal Articleen
dc.contributor.schoolSchool of Physical and Mathematical Sciencesen
dc.identifier.doi10.1039/C4CC09904Den
dc.description.versionPublished versionen
item.grantfulltextopen-
item.fulltextWith Fulltext-
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