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dc.contributor.authorPradhan, Tapan Kumaren_US
dc.contributor.authorLin, Chun Chengen_US
dc.contributor.authorMong, Kwok Kong Tonyen_US
dc.date.accessioned2014-12-08T15:29:39Z-
dc.date.available2014-12-08T15:29:39Z-
dc.date.issued2013-01-01en_US
dc.identifier.issn0936-5214en_US
dc.identifier.urihttp://dx.doi.org/10.1055/s-0032-1317932en_US
dc.identifier.urihttp://hdl.handle.net/11536/21295-
dc.description.abstractPractical synthetic routes to 3-deoxy-D-manno-octulo-sonic acid (KDO) and 3-deoxy-D-arabino-2-heptulosonic acid (DAH) from common sugar substrates are reported. Chain homologation of the sugar substrates was accomplished by Wittig olefination and Corey-Fuchs alkynylation. A new cyclization strategy was investigated to access the desired pyranosyl isomer of the KDO target.en_US
dc.language.isoen_USen_US
dc.subjectcarbohydratesen_US
dc.subjectWittigen_US
dc.subjectCorey-Fuchsen_US
dc.subjectcyclizationen_US
dc.titleFormal Synthesis of 3-Deoxy-D-manno-Octulosonic Acid (KDO) and 3-Deoxy-D-arabino-2-heptulosonic Acid (DAH)en_US
dc.typeArticleen_US
dc.identifier.doi10.1055/s-0032-1317932en_US
dc.identifier.journalSYNLETTen_US
dc.citation.volumeen_US
dc.citation.issue2en_US
dc.citation.spage219en_US
dc.citation.epage222en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000314697700019-
dc.citation.woscount2-
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