Please use this identifier to cite or link to this item: https://doi.org/10.1016/S0040-4039(97)00892-7
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dc.titleConcise synthesis of the cell cycle inhibitor demothoxyfumitremorgin C
dc.contributor.authorWang, H.
dc.contributor.authorGanesan, A.
dc.date.accessioned2014-11-28T02:50:12Z
dc.date.available2014-11-28T02:50:12Z
dc.date.issued1997-06-16
dc.identifier.citationWang, 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.issn00404039
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/111834
dc.description.abstractReaction 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.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1016/S0040-4039(97)00892-7
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentINSTITUTE OF MOLECULAR & CELL BIOLOGY
dc.description.doi10.1016/S0040-4039(97)00892-7
dc.description.sourcetitleTetrahedron Letters
dc.description.volume38
dc.description.issue24
dc.description.page4327-4328
dc.description.codenTELEA
dc.identifier.isiutA1997XE05200038
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