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BEHAVIOR OF STEREOISOMERIC O-METHYLTYROSYL-P-NITROPHENYLALANINES WITHIN THE BETA-CYCLODEXTRIN CAVITY

dc.citation.epage2438en_US
dc.citation.issue23en_US
dc.citation.spage2437en_US
dc.citation.volumeen_US
dc.citation.woscount3
dc.contributor.authorHO, TLen_US
dc.contributor.authorLIAO, PYen_US
dc.contributor.authorWANG, KTen_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.date.accessioned2014-12-08T15:03:00Z
dc.date.available2014-12-08T15:03:00Z
dc.date.issued1995-12-07en_US
dc.description.abstractCyclisation of the L,D- and L,L-O-methyltyrosyl-p-nitrophenylalanine methyl esters is studied; in the presence of beta-cyclodextrin, reaction took place only with the L,L-isomer.en_US
dc.identifier.doi10.1039/c39950002437en_US
dc.identifier.issn0022-4936en_US
dc.identifier.journalJOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONSen_US
dc.identifier.urihttp://dx.doi.org/10.1039/c39950002437en_US
dc.identifier.urihttps://ir.lib.nycu.edu.tw/handle/11536/1603
dc.identifier.wosnumberWOS:A1995TJ04800036
dc.language.isoen_USen_US
dc.titleBEHAVIOR OF STEREOISOMERIC O-METHYLTYROSYL-P-NITROPHENYLALANINES WITHIN THE BETA-CYCLODEXTRIN CAVITYen_US
dc.typeArticleen_US

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