Concise synthesis of the cell cycle inhibitor demothoxyfumitremorgin C

Please use this identifier to cite or link to this item: https://doi.org/10.1016/S0040-4039(97)00892-7

DC Field	Value
dc.title	Concise synthesis of the cell cycle inhibitor demothoxyfumitremorgin C
dc.contributor.author	Wang, H.
dc.contributor.author	Ganesan, A.
dc.date.accessioned	2014-11-28T02:50:12Z
dc.date.available	2014-11-28T02:50:12Z
dc.date.issued	1997-06-16
dc.identifier.citation	Wang, H., Ganesan, A. (1997-06-16). Concise synthesis of the cell cycle inhibitor demothoxyfumitremorgin C. Tetrahedron Letters 38 (24) : 4327-4328. ScholarBank@NUS Repository. https://doi.org/10.1016/S0040-4039(97)00892-7
dc.identifier.issn	00404039
dc.identifier.uri	http://scholarbank.nus.edu.sg/handle/10635/111834
dc.description.abstract	Reaction of the imine derived from L-tryptophan methyl ester and senecialdehyde with Fmoc-L-Pro-Cl induces an acyliminium Pictet-Spengler condensation, yielding a mixture of cis and trans tetrahydro-β-carbolines. Deprotection of the cis product with concomitant diketopiperazine formation afforded the natural product in 20% overall yield.
dc.description.uri	http://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1016/S0040-4039(97)00892-7
dc.source	Scopus
dc.type	Article
dc.contributor.department	INSTITUTE OF MOLECULAR & CELL BIOLOGY
dc.description.doi	10.1016/S0040-4039(97)00892-7
dc.description.sourcetitle	Tetrahedron Letters
dc.description.volume	38
dc.description.issue	24
dc.description.page	4327-4328
dc.description.coden	TELEA
dc.identifier.isiut	A1997XE05200038
Appears in Collections:	Staff Publications

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