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http://hub.abes.fr/acs/periodical/jacsat/1995/volume_117/issue_2/101021ja00107a007/authorship/3
http://hub.abes.fr/acs/periodical/jacsat/1995/volume_117/issue_41/101021ja00146a009/authorship/9
http://hub.abes.fr/acs/periodical/joceah/2003/volume_68/issue_2/101021jo020640f/authorship/5
http://hub.abes.fr/acs/periodical/jacsat/1997/volume_119/issue_34/101021ja971110h/authorship/8
http://hub.abes.fr/acs/periodical/joceah/2005/volume_70/issue_15/101021jo050498t/authorship/8
http://hub.abes.fr/acs/periodical/jacsat/1997/volume_119/issue_34/101021ja971219p/authorship/2
http://hub.abes.fr/acs/periodical/orgnd7/2007/volume_26/issue_19/101021om700311x/authorship/12
http://hub.abes.fr/acs/periodical/joceah/2005/volume_70/issue_1/101021jo048599z/authorship/4
http://hub.abes.fr/acs/periodical/joceah/2003/volume_68/issue_9/101021jo020683w/authorship/10
http://hub.abes.fr/acs/periodical/jacsat/1997/volume_119/issue_34/101021ja971109i/authorship/8
http://hub.abes.fr/acs/periodical/joceah/2002/volume_67/issue_7/101021jo010839c/authorship/3
http://hub.abes.fr/acs/periodical/joceah/2003/volume_68/issue_22/101021jo030228f/authorship/5
http://hub.abes.fr/acs/periodical/joceah/2008/volume_73/issue_12/101021jo8005649/authorship/8
http://hub.abes.fr/acs/periodical/joceah/2006/volume_71/issue_18/101021jo060996h/authorship/9
http://hub.abes.fr/acs/periodical/joceah/2001/volume_66/issue_10/101021jo0102157/authorship/3
http://hub.abes.fr/acs/periodical/joceah/2004/volume_69/issue_7/101021jo0303160/authorship/6
http://hub.abes.fr/acs/periodical/joceah/2001/volume_66/issue_23/101021jo010452/authorship/2
http://hub.abes.fr/acs/periodical/jacsat/1997/volume_119/issue_23/101021ja970619/authorship/5
http://hub.abes.fr/acs/periodical/jacsat/1995/volume_117/issue_2/101021ja00107a009/authorship/5
http://hub.abes.fr/acs/periodical/joceah/1992/volume_57/issue_26/101021jo00052a046/authorship/1
http://hub.abes.fr/acs/periodical/joceah/1992/volume_57/issue_14/101021jo00040a059/authorship/1
http://hub.abes.fr/acs/periodical/joceah/1992/volume_57/issue_26/101021jo00052a602/authorship/1
http://hub.abes.fr/acs/periodical/jacsat/1995/volume_117/issue_33/101021ja00138a035/authorship/3
http://hub.abes.fr/acs/periodical/jacsat/1995/volume_117/issue_2/101021ja00107a008/authorship/2
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Correction. A Novel Synthesis of the Dibenz-[b,f]oxepin Ring System: 10,11-Dihydro-11-hydroxydibenz[b,f]oxepin-10(11H)-one
A novel synthesis of the dibenz[b,f]oxepin ring system: 10,11-dihydro-11-hydroxydibenz[b,f]oxepin-10(11H)-one
Total Synthesis of Brevetoxin B. 2. Second Generation Strategies and Construction of the Dioxepane Region [DEFG]
Total synthesis of Taxol. 2. construction of A and C ring intermediates and initial attempts to construct the ABC ring system. [Erratum to document cited in CA122:160984]
Palladium-Catalyzed CarbonylativeAnnulation of o-Alkynylphenols: Synthesesof 2-Substituted-3-aroyl-benzo[b]furans
Total Synthesis of Methyl Protodioscin: A Potent Agent withAntitumor Activity
Palladium-Catalyzed Functionalization of Lactonesvia Their Cyclic Ketene Acetal Phosphates.Efficient New Synthetic Technology for theConstruction of Medium and Large Cyclic Ethers
Total Synthesis of Wedelolactone
Pd-Catalyzed Copper-Free CarbonylativeSonogashira Reaction of Aryl Iodides withAlkynes for the Synthesis of AlkynylKetones and Flavones by Using Water as aSolvent
Synthesis of Catechins via Thiourea/AuCl3-Catalyzed Cycloalkylation of Aryl Epoxides
Synthesis of Thiourea−Oxazolines, a New Class of ChiralS,N-Heterobidentate Ligands: Application in Pd-CatalyzedAsymmetric Bis(methoxycarbonylation) of Terminal Olefins
Total Syntheses of Epothilones A and B via aMacrolactonization-Based Strategy
New Synthetic Technology for the Construction of9-Membered Ring Cyclic Ethers. Construction ofthe EFGH Ring Skeleton of Brevetoxin A
The Olefin Metathesis Approach to Epothilone A and ItsAnalogues
Palladium-Catalyzed Cross-CouplingReactions of 4-Tosyl-2(5H)-furanone withBoronic Acids: A Facile and EfficientRoute to Generate 4-Substituted2(5H)-Furanones
Synthetic Study of 1,3-Butadiene-Based IMDA Approach toConstruct a [5−7−6] Tricyclic Core and Its Application to the TotalSynthesis of C8-epi-Guanacastepene O
Nickel-Catalyzed Cross-Couplings of4-Diethylphosphonooxycoumarins withOrganozinc Reagents: An Efficient NewMethodology for the Synthesis of4-Substituted Coumarins
Synthesis of 4-Substituted Coumarins viathe Palladium-Catalyzed Cross-Couplingsof 4-Tosylcoumarins with TerminalAcetylenes and Organozinc Reagents
Synthesis of Conformationally Restricted 2,3-Diarylbenzo[b]furanby the Pd-Catalyzed Annulation of o-Alkynylphenols: Exploring aCombinatorial Approach
Total Synthesis of Taxol. 4. The Final Stages and Completion of the Synthesis
Total Synthesis of Taxol. 3. Formation of Taxol's ABC Ring Skeleton
Total Synthesis of taxol. 2. Construction of A and C ring intermediates and initial attempts to construct the ABC ring system
Compounds from Danshen. Part 7. Regioselective introduction of carbon-3 substituents to 5-alkyl-7-methoxy-2-phenylbenzo[b]furans: synthesis of a novel adenosine A1 receptor ligand and its derivatives
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