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dc.contributor.authorChen, Chih-Hauen_US
dc.contributor.authorChang, Chia-Maoen_US
dc.contributor.authorChen, Hsia-Yuanen_US
dc.contributor.authorLai, Jin-Jien_US
dc.contributor.authorSun, Chung-Mingen_US
dc.date.accessioned2014-12-08T15:13:40Z-
dc.date.available2014-12-08T15:13:40Z-
dc.date.issued2007-07-01en_US
dc.identifier.issn1520-4766en_US
dc.identifier.urihttp://dx.doi.org/10.1021/cc070035wen_US
dc.identifier.urihttp://hdl.handle.net/11536/10574-
dc.description.abstractPharmacologically interesting tetrahydro-beta-carbolinehydantoins have been prepared through four-step traceless synthesis by a combinatorial approach. Two-arm PEG 1 (MW approximate to 4000) was used as a soluble polymer support and reacted with Fmoc-protected L-tryptophane 2 to form bis-ester 3. The resulting polymer-supported amino ester 3 was deprotected, and amino ester 4 underwent Pictet-Spengler reaction with varoius ketones to form tricyclic indoles 5. The nucleophilic piperidine in the tricyclic indole reacted with isocyanate to generate the urea intermediates and simultaneously intramolecular cyclization to release the target compounds 7 from the support in good yields.en_US
dc.language.isoen_USen_US
dc.titleScaffold-directed traceless synthesis of tetrahydro-beta-carbolinehydantoinsen_US
dc.typeArticleen_US
dc.identifier.doi10.1021/cc070035wen_US
dc.identifier.journalJOURNAL OF COMBINATORIAL CHEMISTRYen_US
dc.citation.volume9en_US
dc.citation.issue4en_US
dc.citation.spage618en_US
dc.citation.epage626en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000247820100010-
dc.citation.woscount11-
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