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Efficient synthetic method of Psammaplin A

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dc.contributor.authorHong, Suckchang-
dc.contributor.authorLee, Myungmo-
dc.contributor.authorJung, Myunggi-
dc.contributor.authorPark, Yohan-
dc.contributor.authorKim, Mi-hyun-
dc.contributor.authorPark, Hyeung-geun-
dc.date.accessioned2024-05-14T07:18:49Z-
dc.date.available2024-05-14T07:18:49Z-
dc.date.created2017-11-15-
dc.date.issued2012-08-
dc.identifier.citationTetrahedron Letters, Vol.53 No.32, pp.4209-4211-
dc.identifier.issn0040-4039-
dc.identifier.urihttps://hdl.handle.net/10371/202030-
dc.description.abstractA new concise and efficient synthetic method of Psammaplin A was developed. Psammaplin A was obtained with 50% overall yield in nine steps from p-hydroxybenzaldehyde and ethyl acetoacetate via Knoevenagel condensation and direct nitrosation as key steps. This method might be very efficient to construct a quite diverse library of Psammaplin A type analogs. (C) 2012 Elsevier Ltd. All rights reserved.-
dc.language영어-
dc.publisherElsevier BV-
dc.titleEfficient synthetic method of Psammaplin A-
dc.typeArticle-
dc.identifier.doi10.1016/j.tetlet.2012.05.149-
dc.citation.journaltitleTetrahedron Letters-
dc.identifier.wosid000306766200044-
dc.identifier.scopusid2-s2.0-84863628529-
dc.citation.endpage4211-
dc.citation.number32-
dc.citation.startpage4209-
dc.citation.volume53-
dc.description.isOpenAccessN-
dc.contributor.affiliatedAuthorHong, Suckchang-
dc.contributor.affiliatedAuthorPark, Hyeung-geun-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.subject.keywordPlusRESISTANT STAPHYLOCOCCUS-AUREUS-
dc.subject.keywordPlusSPONGE-
dc.subject.keywordPlusMETABOLITES-
dc.subject.keywordPlusCELLS-
dc.subject.keywordPlusMRSA-
dc.subject.keywordAuthorTotal synthesis-
dc.subject.keywordAuthorPsammaplin A-
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Related Researcher

  • College of Pharmacy
  • Department of Manufacturing Pharmacy
Research Area Development of methodologies using metal catalyst, Total synthesis of natural products

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