Total synthesis of the cytotoxic alkaloid luotonin A

Please use this identifier to cite or link to this item: https://scholarbank.nus.edu.sg/handle/10635/112140

DC Field	Value
dc.title	Total synthesis of the cytotoxic alkaloid luotonin A
dc.contributor.author	Wang, H.
dc.contributor.author	Ganesan, A.
dc.date.accessioned	2014-11-28T02:53:39Z
dc.date.available	2014-11-28T02:53:39Z
dc.date.issued	1998-12-03
dc.identifier.citation	Wang, 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.issn	00404039
dc.identifier.uri	http://scholarbank.nus.edu.sg/handle/10635/112140
dc.description.abstract	The 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.source	Scopus
dc.subject	Alkaloids
dc.subject	Cytotoxins
dc.subject	Natural producs
dc.subject	Quinazolinones
dc.type	Article
dc.contributor.department	INSTITUTE OF MOLECULAR & CELL BIOLOGY
dc.description.sourcetitle	Tetrahedron Letters
dc.description.volume	39
dc.description.issue	49
dc.description.page	9097-9098
dc.description.coden	TELEA
dc.identifier.isiut	NOT_IN_WOS
Appears in Collections:	Staff Publications

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