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dc.contributor.author이용록ko
dc.contributor.author이신ko
dc.date.accessioned2015-12-17T05:00:37Z-
dc.date.available2015-12-17T05:00:37Z-
dc.date.created2015-11-13-
dc.date.issued201402-
dc.identifier.citationORGANIC & BIOMOLECULAR CHEMISTRY, v.12, no.8, pp.1250 - 1257-
dc.identifier.issn1477-0520-
dc.identifier.urihttp://hdl.handle.net/YU.REPOSITORY/33194-
dc.identifier.urihttp://dx.doi.org/10.1039/c3ob42110d-
dc.description.abstractSimple and facile synthetic routes for the preparation of biologically interesting cyclol bearing polycycles were developed using FeCl3-promoted [2 + 2] cycloaddition from readily available benzopyrans possessing a variety of substituents. As examples of this methodology, one-step syntheses of cannabicyclol, cannabicyclovarin, and ranhuadujuanine A were accomplished in good yield.-
dc.language영어-
dc.publisherROYAL SOC CHEMISTRY-
dc.subjectRHODODAURICHROMANIC-ACID-A-
dc.subjectDIELS-ALDER REACTION-
dc.subjectPYRANOCHALCONE NATURAL-PRODUCTS-
dc.subjectCONCISE TOTAL-SYNTHESIS-
dc.subjectARTOCARPUS-RIGIDA-
dc.subjectALPHA,BETA-UNSATURATED ALDEHYDES-
dc.subject2-PI+2-PI CYCLOADDITION-
dc.subjectRHODODENDRON-DAURICUM-
dc.subjectCANNABINOID RECEPTOR-
dc.subjectMORACEAE PLANTS-
dc.titleEfficient and novel one-pot synthesis of polycycles bearing cyclols by FeCl3-promoted [2+2] cycloaddition: application to cannabicyclol, cannabicyclovarin, and ranhuadujuanine A-
dc.typeArticle-
dc.identifier.wosid000330792500011-
dc.identifier.scopusid2-s2.0-84893235254-
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공과대학 > 화학공학부 > Articles
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