Please use this identifier to cite or link to this item: https://scholarbank.nus.edu.sg/handle/10635/112140
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dc.titleTotal synthesis of the cytotoxic alkaloid luotonin A
dc.contributor.authorWang, H.
dc.contributor.authorGanesan, A.
dc.date.accessioned2014-11-28T02:53:39Z
dc.date.available2014-11-28T02:53:39Z
dc.date.issued1998-12-03
dc.identifier.citationWang, H.,Ganesan, A. (1998-12-03). Total synthesis of the cytotoxic alkaloid luotonin A. Tetrahedron Letters 39 (49) : 9097-9098. ScholarBank@NUS Repository.
dc.identifier.issn00404039
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/112140
dc.description.abstractThe structure of luotonin A was unambiguously confirmed by total synthesis. Deprotonation of 3-oxo-1H-pyrrolo[3,4-b]quinoline gave an anion which was coupled with 2-sulfinylaminobenzoyl chloride (prepared by reaction of anthranilic acid with thionyl chloride) to afford the natural product in 85% yield.
dc.sourceScopus
dc.subjectAlkaloids
dc.subjectCytotoxins
dc.subjectNatural producs
dc.subjectQuinazolinones
dc.typeArticle
dc.contributor.departmentINSTITUTE OF MOLECULAR & CELL BIOLOGY
dc.description.sourcetitleTetrahedron Letters
dc.description.volume39
dc.description.issue49
dc.description.page9097-9098
dc.description.codenTELEA
dc.identifier.isiutNOT_IN_WOS
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