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dc.contributor.author이용록ko
dc.contributor.author네우판프라틱ko
dc.contributor.author하립개ko
dc.date.accessioned2015-12-17T04:06:24Z-
dc.date.available2015-12-17T04:06:24Z-
dc.date.created2015-11-13-
dc.date.issued201408-
dc.identifier.citationADVANCED SYNTHESIS & CATALYSIS, v.356, no.11-12, pp.2566 - 2574-
dc.identifier.issn1615-4150-
dc.identifier.urihttp://hdl.handle.net/YU.REPOSITORY/31274-
dc.identifier.urihttp://dx.doi.org/10.1002/adsc.201301086-
dc.description.abstractAn efficient one-pot method is described for the synthesis of a variety of di- and trisubstituted 4-pyrones based on the gold-catalyzed cascade reactions between cyclic or acyclic diazodicarbonyl compounds and vinyl ethers. The key strategy used involves the gold-catalyzed Wolff rearrangement of diazo compounds followed by [4+2] cycloaddition and elimination. This methodology is also applied to the synthesis of tetrasubstituted 4-pyrones.-
dc.language영어-
dc.publisherWILEY-V C H VERLAG GMBH-
dc.subjectCYCLIC DIAZODICARBONYL COMPOUNDS-
dc.subjectHIGHLY SUBSTITUTED FURANS-
dc.subjectPYRONE NATURAL-PRODUCTS-
dc.subjectH INSERTION REACTIONS-
dc.subjectGAMMA-PYRONE-
dc.subjectRHODIUM(II)-CATALYZED REACTIONS-
dc.subjectEFFICIENT SYNTHESIS-
dc.subjectENANTIOSELECTIVE INSERTION-
dc.subjectSTREPTOMYCES-SPECTABILIS-
dc.subjectAEROBIC OXIDATION-
dc.titleOne-Pot Synthesis of Multi-Substituted 4-Pyrones by a Gold-Catalyzed Cascade of Wolff Rearrangement/[4+2] Cycloaddition/Elimination Reactions-
dc.typeArticle-
dc.identifier.wosid000340567100022-
dc.identifier.scopusid2-s2.0-84906228600-
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공과대학 > 화학공학부 > Articles
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