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dc.contributor.authorSenthilvelan, Annamalaien_US
dc.contributor.authorTsai, Ming-Tsungen_US
dc.contributor.authorChang, Kai-Chien_US
dc.contributor.authorChung, Wen-Shengen_US
dc.date.accessioned2014-12-08T15:15:12Z-
dc.date.available2014-12-08T15:15:12Z-
dc.date.issued2006-12-18en_US
dc.identifier.issn0040-4039en_US
dc.identifier.urihttp://dx.doi.org/10.1016/j.tetlet.2006.10.082en_US
dc.identifier.urihttp://hdl.handle.net/11536/11433-
dc.description.abstractMO(CO)(6)-mediated ring opening reactions of calix[4]arene isoxazolines/isoxazoles provide a new synthetic methodology for calix[4]arenes carrying bifunctional beta-hydroxy ketones or alpha,beta-unsaturated-beta-amino ketones. MO(CO)(6) is a highly selective and convenient reagent for the ring opening process of these supramolecular isoxazolines/isoxazoles. (c) 2006 Elsevier Ltd. All rights reserved.en_US
dc.language.isoen_USen_US
dc.subjectcalix[4]arene isoxazolines/isoxazolesen_US
dc.subjectmolybdenum hexacarbonylen_US
dc.subjectbeta-hydroxy ketonesen_US
dc.subjectalpha,beta-unsaturated-beta-amino ketonesen_US
dc.titleMO(CO)(6)-mediated synthesis of calix[4]arenes carrying beta-hydroxy ketones or alpha,beta-unsaturated-beta-amino ketonesen_US
dc.typeArticleen_US
dc.identifier.doi10.1016/j.tetlet.2006.10.082en_US
dc.identifier.journalTETRAHEDRON LETTERSen_US
dc.citation.volume47en_US
dc.citation.issue51en_US
dc.citation.spage9077en_US
dc.citation.epage9081en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000242556000015-
dc.citation.woscount11-
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