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dc.contributor.authorLin, Shih-Cheen_US
dc.contributor.authorChao, Chin-Shengen_US
dc.contributor.authorChang, Chiu-Chingen_US
dc.contributor.authorMong, Kwok-Kong T.en_US
dc.date.accessioned2014-12-08T15:07:03Z-
dc.date.available2014-12-08T15:07:03Z-
dc.date.issued2010-04-07en_US
dc.identifier.issn0040-4039en_US
dc.identifier.urihttp://dx.doi.org/10.1016/j.tetlet.2010.02.021en_US
dc.identifier.urihttp://hdl.handle.net/11536/5522-
dc.description.abstractJoined use of N-benzyl oxazolidinone and N-benzyl-N-benzyloxycarbonyl (N-BnCbz) desymmetric amino-protecting function is reported. The new synthetic approach enables the facile preparation of type I and type 2 LacNAc disaccharides in satisfactory yields. One-pot deprotection of N-BnCbz and O-benzyl ether is achieved by hydrogenolysis under mild conditions. (C) 2010 Elsevier Ltd. All rights reserved.en_US
dc.language.isoen_USen_US
dc.titleJoined use of oxazolidinone and desymmetric amino protection: a new strategy for protection of glucosamineen_US
dc.typeArticleen_US
dc.identifier.doi10.1016/j.tetlet.2010.02.021en_US
dc.identifier.journalTETRAHEDRON LETTERSen_US
dc.citation.volume51en_US
dc.citation.issue14en_US
dc.citation.spage1910en_US
dc.citation.epage1913en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000275920600026-
dc.citation.woscount4-
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