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dc.contributor.authorTsai, CSen_US
dc.contributor.authorLi, YKen_US
dc.contributor.authorLo, LCen_US
dc.date.accessioned2014-12-08T15:41:49Z-
dc.date.available2014-12-08T15:41:49Z-
dc.date.issued2002-10-17en_US
dc.identifier.issn1523-7060en_US
dc.identifier.urihttp://dx.doi.org/10.1021/ol0265315en_US
dc.identifier.urihttp://hdl.handle.net/11536/28446-
dc.description.abstract[GRAPHICS] A new synthetic route was developed for the preparation of activity probe 1 for beta-glucosidase in this study. The key glycosidation step begins with benzyl p-hydroxyphenylacetate. Benzylic functionalization for the construction of the trapping device was achieved at later stages. Probe 1 was shown to be able to label the target enzyme. This cassette-like design offers great flexibility for future alterations. It would allow the synthetic scheme to expand to other glycosidase probes with different linker/reporter combinations.en_US
dc.language.isoen_USen_US
dc.titleDesign and synthesis of activity probes for glycosidasesen_US
dc.typeArticleen_US
dc.identifier.doi10.1021/ol0265315en_US
dc.identifier.journalORGANIC LETTERSen_US
dc.citation.volume4en_US
dc.citation.issue21en_US
dc.citation.spage3607en_US
dc.citation.epage3610en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000178522700015-
dc.citation.woscount51-
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