Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/163038
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dc.contributor.authorChiu, Angela Qi Yunen_US
dc.contributor.authorKrishna, Rameshen_US
dc.contributor.authorPhyo, Ma Yadanaren_US
dc.contributor.authorSae-Lao, Patcharapornen_US
dc.contributor.authorBates, Roderick Waylanden_US
dc.date.accessioned2022-11-22T02:19:41Z-
dc.date.available2022-11-22T02:19:41Z-
dc.date.issued2022-
dc.identifier.citationChiu, A. Q. Y., Krishna, R., Phyo, M. Y., Sae-Lao, P. & Bates, R. W. (2022). Synthesis of penicolinates A, C and D. Heterocycles, 105(1), 588-593. https://dx.doi.org/10.3987/COM-22-S(R)15en_US
dc.identifier.issn1881-0942en_US
dc.identifier.urihttps://hdl.handle.net/10356/163038-
dc.description.abstractPenicolinates A, C and D are synthesized using the Sonogashira coupling reaction as a key step. By comparison of the optical rotation, the stereochemistry of penicolinate D is determined to be (S).en_US
dc.description.sponsorshipNanyang Technological Universityen_US
dc.description.sponsorshipNational Research Foundation (NRF)en_US
dc.language.isoenen_US
dc.relationNRF–CRP18–2017–01en_US
dc.relation.ispartofHeterocyclesen_US
dc.rights© 2022 The Japan Institute of Heterocyclic Chemistry. All rights reserved.en_US
dc.subjectScience::Chemistryen_US
dc.titleSynthesis of penicolinates A, C and Den_US
dc.typeJournal Articleen
dc.contributor.schoolSchool of Physical and Mathematical Sciencesen_US
dc.identifier.doi10.3987/COM-22-S(R)15-
dc.identifier.issue1en_US
dc.identifier.volume105en_US
dc.identifier.spage588en_US
dc.identifier.epage593en_US
dc.subject.keywordsPenicolinates A and Cen_US
dc.subject.keywordsOrganic Compoundsen_US
dc.description.acknowledgementThis research was supported by the National Research Foundation (NRF) Singapore, NRF Competitive Research Programme (CRP), Grant Award Number NRF–CRP18–2017–01. We also thank NTU for financial support.en_US
item.grantfulltextnone-
item.fulltextNo Fulltext-
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