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postgraduate thesis: Studies toward the total synthesis of pseudolaric acid B via an improved carbene cyclization cycloaddition cascade strategy

TitleStudies toward the total synthesis of pseudolaric acid B via an improved carbene cyclization cycloaddition cascade strategy
Authors
Advisors
Advisor(s):Chiu, P
Issue Date2014
PublisherThe University of Hong Kong (Pokfulam, Hong Kong)
Citation
Li, B. [李保健]. (2014). Studies toward the total synthesis of pseudolaric acid B via an improved carbene cyclization cycloaddition cascade strategy. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5295521
DegreeDoctor of Philosophy
SubjectAntifungal agents
Diterpenes - Synthesis
Dept/ProgramChemistry
Persistent Identifierhttp://hdl.handle.net/10722/202371

 

DC FieldValueLanguage
dc.contributor.advisorChiu, P-
dc.contributor.authorLi, Baojian-
dc.contributor.author李保健-
dc.date.accessioned2014-09-18T02:28:15Z-
dc.date.available2014-09-18T02:28:15Z-
dc.date.issued2014-
dc.identifier.citationLi, B. [李保健]. (2014). Studies toward the total synthesis of pseudolaric acid B via an improved carbene cyclization cycloaddition cascade strategy. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5295521-
dc.identifier.urihttp://hdl.handle.net/10722/202371-
dc.languageeng-
dc.publisherThe University of Hong Kong (Pokfulam, Hong Kong)-
dc.relation.ispartofHKU Theses Online (HKUTO)-
dc.rightsThe author retains all proprietary rights, (such as patent rights) and the right to use in future works.-
dc.rightsCreative Commons: Attribution 3.0 Hong Kong License-
dc.subject.lcshAntifungal agents-
dc.subject.lcshDiterpenes - Synthesis-
dc.titleStudies toward the total synthesis of pseudolaric acid B via an improved carbene cyclization cycloaddition cascade strategy-
dc.typePG_Thesis-
dc.identifier.hkulb5295521-
dc.description.thesisnameDoctor of Philosophy-
dc.description.thesislevelDoctoral-
dc.description.thesisdisciplineChemistry-
dc.description.naturepublished_or_final_version-
dc.identifier.doi10.5353/th_b5295521-

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