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dc.contributor.authorPatil, Pratap S.en_US
dc.contributor.authorLee, Chia-Chenen_US
dc.contributor.authorHuang, Yu-Wenen_US
dc.contributor.authorZulueta, Medel Manuel L.en_US
dc.contributor.authorHung, Shang-Chengen_US
dc.date.accessioned2014-12-08T15:30:29Z-
dc.date.available2014-12-08T15:30:29Z-
dc.date.issued2013en_US
dc.identifier.issn1477-0520en_US
dc.identifier.urihttp://hdl.handle.net/11536/21786-
dc.identifier.urihttp://dx.doi.org/10.1039/c3ob40079den_US
dc.description.abstractOligosaccharide syntheses are an important source of well-defined sugar constructs particularly needed for the evaluation of structure-activity relationships. The chemical assembly of oligosaccharides requires several building blocks, that is, glycosyl donors and acceptors, which are prepared in multistep processes and in a generally tedious and time-consuming manner. Having developed one-pot procedures meant to minimise the effort in sugar building block preparation, we tackled herein the one-pot preparation of fully protected and 2-, 3-, 4-, and 6-alcohol derivatives of D-mannose, a widely distributed monosaccharide. As a consequence of the hydroxyl group pattern of D-mannose, regioselective and stereoselective benzylide-nations were developed and later seamlessly utilised as the first transformation in the one-pot procedure.en_US
dc.language.isoen_USen_US
dc.titleRegioselective and stereoselective benzylidene installation and one-pot protection of D-mannoseen_US
dc.typeArticleen_US
dc.identifier.doi10.1039/c3ob40079den_US
dc.identifier.journalORGANIC & BIOMOLECULAR CHEMISTRYen_US
dc.citation.volume11en_US
dc.citation.issue16en_US
dc.citation.spage2605en_US
dc.citation.epage2612en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000316803900009-
dc.citation.woscount8-
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