about
A concise enantioselective synthesis of (-)-ranirestat.Male-produced pheromone of Spathius agrili, a parasitoid introduced for the biological control of the invasive emerald ash borer, Agrilus planipennis.Total syntheses and biological reassessment of lactimidomycin, isomigrastatin and congener glutarimide antibiotics.Design, synthesis, and evaluation of curcumin-derived arylheptanoids for glioblastoma and neuroblastoma cytotoxicityA carbohydrate approach for the formal total synthesis of (-)-aspergillide C.Structurally and stereochemically diverse tetrahydropyran synthesis through oxidative C-H bond activation.Transition-metal-catalyzed synthesis of aspergillide B: an alkyne addition strategy.Dinuclear zinc-catalyzed asymmetric desymmetrization of acyclic 2-substituted-1,3-propanediols: a powerful entry into chiral building blocks.Synthesis of bridged inside-outside bicyclic ethers through oxidative transannular cyclization reactions.Sequential Processes in Palladium-Catalyzed Silicon-Based Cross-Coupling.Alkyne hydrosilylation catalyzed by a cationic ruthenium complex: efficient and general trans addition.Broad Spectrum Enolate Equivalent for Catalytic Chemo-, Diastereo-, and Enantioselective Addition to N-Boc Imines.Asymmetric total synthesis of soraphen A: a flexible alkyne strategyIntermolecular silacarbonyl ylide cycloadditions: a direct pathway to oxasilacyclopentenes.Development of Zn-ProPhenol-catalyzed asymmetric alkyne addition: synthesis of chiral propargylic alcohols.Formation of Ruthenium Carbenes by gem-Hydrogen Transfer to Internal Alkynes: Implications for Alkyne trans-Hydrogenation.Total Synthesis, Stereochemical Assignment, and Field-Testing of the Sex Pheromone of the Strepsipteran Xenos peckii.Enantioselective ProPhenol-catalyzed addition of 1,3-diynes to aldehydes to generate synthetically versatile building blocks and diyne natural products.Formation of ruthenium carbenes by gem-hydrogen transfer to internal alkynes: implications for alkyne trans-hydrogenation.De novo synthesis of D- and L-fucosamine containing disaccharides.Kinetic resolution in asymmetric epoxidation using iminium salt catalysis.Relay cross metathesis reactions of vinylphosphonates.Synthesis of cyclooxygenase metabolites of 8,9-epoxyeicosatrienoic acid (EET): 11- and 15-hydroxy 8,9-EETs.Iron pincer complex catalyzed, environmentally benign, E-selective semi-hydrogenation of alkynes.Alkyne metathesis on the rise.Enantioselective Synthesis of Trisubstituted Allenyl-B(pin) Compounds by Phosphine-Cu-Catalyzed 1,3-Enyne Hydroboration. Insights Regarding Stereochemical Integrity of Cu-Allenyl Intermediates.Combining visible light catalysis and transfer hydrogenation for in situ efficient and selective semihydrogenation of alkynes under ambient conditions.Intramolecular Formal anti-Carbopalladation/Heck Reaction: Facile Domino Access to Carbo- and Heterooligocyclic Dienes.A trans-selective hydroboration of internal alkynes.Catalytic Stereoselective Semihydrogenation of Alkynes toE-AlkenesAllylpalladium(II) Histidylidene Complexes and Their Application inZ-Selective Transfer Semihydrogenation of AlkynesHydrosilylation of Internal Alkynes Catalyzed by Tris- Imidazolium Salt-Stabilized Palladium NanoparticlesFormalanti-Carbopalladation Reactions of Non-Activated Alkynes: Requirements, Mechanistic Insights, and ApplicationsFormaleanti-Carbopalladierungen nicht-aktivierter Alkine: Voraussetzungen, mechanistische Untersuchungen und Anwendungen
P2860
Q33771896-EF121606-CE9E-4C11-9CDE-088873FB674BQ34211300-2C4B4DF0-CF61-4E50-A6B5-079BECE5DA56Q34339977-C96850AB-E604-4076-9097-18D962F0AB9EQ34555833-C5EBB284-D836-4F51-90C0-F95825A675A6Q35030667-BB50A3C5-3417-434A-9865-F910BCF0FA01Q35117493-0FD6D349-E8F5-4275-A4FB-6B5C8F5F8CE1Q36125691-C9C5B9A3-3745-48E8-96C4-9B381FFF35D9Q36381488-8397FE6E-D39C-4E70-A1A7-4977A325FE21Q36400072-38A26891-C98D-49E4-BA42-F1E2FF6A4F94Q36503121-A87FF0BD-87C5-46D5-B487-8D8BF03A5931Q36868811-563B282D-3988-4FC7-93BA-3F9CDBAB3DF9Q36900345-81B45D7D-4CB7-4DA0-82C4-B74153D7BF42Q36996663-8FEFDAD6-4107-4C20-AF0E-2E793BFBCC33Q37147584-4F88D346-EFE5-4E69-B8DA-56EE38A032ADQ37395796-A970CB4D-1947-4A71-8A30-2CEDF51CD6E4Q39539281-69AF15CD-2F9D-49DD-ACB9-045E4EE42A0DQ39899846-167FD81D-B40B-40A4-85F1-12AE8BD653F0Q40366378-3E2003CF-81CF-43F6-BCD0-811FAC7E45F5Q40581797-A65B71A3-E320-4E3D-AE61-F54525E1E24DQ41192160-5E524D3E-502C-4D5A-8005-F54557C3C109Q41972435-33ABE7C9-F081-4262-9A7D-1565978111FBQ42906428-A232EB23-6ED0-4DBC-ABDA-8E7CD423C02EQ45968882-E57CEA97-F19A-4202-BC00-2F07FDF275B1Q46244478-F8EE2CEA-25EF-45AF-8927-0A86F4437949Q46735134-492C7678-684F-4ABA-A864-2586D93770CDQ50124413-A6115006-5B94-4439-8BD4-CD2ABE7025DDQ51634737-884E11E2-F47E-4432-8A02-309F1B122ABBQ53595938-FD5E5317-5BDF-46B8-8A07-177ADAE09F06Q54671407-486D25C9-B257-49CC-827E-DC3D8631D25AQ56690363-B15979C7-A843-4AEF-A5B2-9A7F2132B486Q56741688-515ACF10-16D8-4E32-B5D2-346624195DA5Q57832593-DBE49A41-F8FB-4DC9-904C-99594FFE5F7FQ57905656-07958667-5642-44E5-9CEF-6647559E0B84Q57905657-7CB49D00-F726-4EAD-BEF0-4904F867B094
P2860
description
2002 nî lūn-bûn
@nan
2002年の論文
@ja
2002年学术文章
@wuu
2002年学术文章
@zh
2002年学术文章
@zh-cn
2002年学术文章
@zh-hans
2002年学术文章
@zh-my
2002年学术文章
@zh-sg
2002年學術文章
@yue
2002年學術文章
@zh-hant
name
A chemoselective reduction of alkynes to (E)-alkenes.
@en
A chemoselective reduction of alkynes to
@nl
type
label
A chemoselective reduction of alkynes to (E)-alkenes.
@en
A chemoselective reduction of alkynes to
@nl
prefLabel
A chemoselective reduction of alkynes to (E)-alkenes.
@en
A chemoselective reduction of alkynes to
@nl
P356
P1476
A chemoselective reduction of alkynes to (E)-alkenes.
@en
P2093
Thomas Jöge
Zachary T Ball
P304
P356
10.1021/JA026457L
P407
P50
P577
2002-07-01T00:00:00Z