Highly general stereo-, regio-, and chemo-selective synthesis of terminal and internal conjugated enynes by the Pd-catalysed reaction of alkynylzinc reagents with alkenyl halides
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Computational protein engineering: bridging the gap between rational design and laboratory evolution.Chiral organoborane Lewis pairs derived from pyridylferrocene.Rational exploration of N-heterocyclic carbene (NHC) palladacycle diversity: a highly active and versatile precatalyst for Suzuki-Miyaura coupling reactions of deactivated aryl and alkyl substrates.Higher-order zincates as transmetalators in alkyl-alkyl negishi cross-coupling.Halogen-enriched fragment libraries as chemical probes for harnessing halogen bonding in fragment-based lead discovery.Highly stereoselective total synthesis of fully hydroxy-protected mycolactones A and B and their stereoisomerization upon deprotectionMicrowave-assisted C-C bond forming cross-coupling reactions: an overview.Insights into the elementary steps in Negishi coupling through kinetic investigations.Synthesis of binaphthyl based phosphine and phosphite ligands.Fluorometric imaging methods for palladium and platinum and the use of palladium for imaging biomolecules.Cyclic enaminones. Part II: applications as versatile intermediates in alkaloid synthesis.Regioselective synthesis of naphthoquinone/naphthoquinol-carbohydrate hybrids by [4 + 2] anionic annulations and studies on their cytotoxicity.Oxidative addition of the C-I bond on aluminum nanoclusters.Acylboranes: synthetic strategies and applications.Total syntheses of cyanthiwigins B, F, and G.Di-Zinc-Aryl Complexes: CO2 Insertions and Applications in Polymerisation Catalysis.Quantitative Structure-Retention Relationships for Polycyclic Aromatic Hydrocarbons and their Oligoalkynyl-Substituted Derivatives.Miniaturized catalysis: monolithic, highly porous, large surface area capillary flow reactors constructed in situ from polyhedral oligomeric silsesquioxanes (POSS).Synthesis and structural diversity of oligosilanylzinc compounds.Synthetically important alkali-metal utility amides: lithium, sodium, and potassium hexamethyldisilazides, diisopropylamides, and tetramethylpiperidides.Generation of an 4-Isoxazolyl Anion Species: Facile Access to Multifunctionalized Isoxazoles.Generation of functionalized aryl and heteroaryl aluminum reagents by halogen-lithium exchange.1,4-Pentenyne as a five-carbon synthon for efficient and selective syntheses of natural products containing 2,4-dimethyl-1-penten-1,5-ylidene and related moieties by means of Zr-catalyzed carboalumination of alkynes and alkenes.Ferrocenes with perfluorinated side chains and ferrocenophanes with fluorinated handles.Autocatalytic formation of fluorinated ferrocenophanes from 1,1'-bis(trifluorovinyl)ferrocene.Negishi cross-couplings in the synthesis of amino acids.Zn-, Mg-, and Li-TMP Bases for the Successive Regioselective Metalations of the 1,5-Naphthyridine Scaffold (TMP=2,2,6,6-Tetramethylpiperidyl).Preparation of Solid Polyfunctional Alkynylzinc Pivalates with Enhanced Air and Moisture Stability for Organic Synthesis.A Divergent Approach to the Marine Diterpenoids (+)-Dictyoxetane and (+)-Dolabellane V.Cathodic Aromatic C,C Cross-Coupling Reaction via Single Electron Transfer Pathway.Oxidant-free dehydrogenative coupling reactions via hydrogen evolution.Rhodium(III)-catalyzed olefinic C-H alkynylation of enamides at room temperature.Palladium-catalyzed cross-coupling of unactivated alkenes with acrylates: application to the synthesis of the C13-C21 fragment of palmerolide A.Synthesis, reactivity and applications of zinc-zinc bonded complexes.Inhibiting copper(I) iodide aggregate assembly in the solid state via macrocyclic encapsulation.Calcium carbide catalytically activated with tetra-n-butyl ammonium fluoride for Sonogashira cross coupling reactionsGeneral Strategies for the Synthesis of Liquid CrystalsPhenol Based-Ligands with Two AdjacentN,N′,O-Binding Pockets
P2860
Q30394571-C7CDD591-F019-47C7-8484-DA1AFD440713Q30830478-1581CA95-9414-4C2F-87FC-B3717D8D138AQ33533417-9A04572A-A076-4877-B5E5-E5B2BFE8E1CDQ34280337-D3EF4354-7715-4BF3-A266-8498ACD89CFEQ35181268-E80CA29D-C1EC-4FAE-A2B6-92B652FA5806Q37296425-6902014E-4ABD-4131-BFAB-C6200E37891FQ37895951-38B609D2-A030-41BF-984E-D3F32B4C120BQ38029252-B10B60BE-5685-4581-AB84-DE491A972717Q38115696-6CBE486C-F197-474A-B7F8-EC074BE3D8E4Q38364149-C0E5F45A-93CD-4FF2-8773-E6256A530FC6Q38613546-5E5CBFC7-7502-46A5-AC49-0D1F07F47D5EQ38736749-4325B0E2-113C-47E0-98CA-3746A4DDB159Q38990051-F771B7AB-0850-4BFB-ABFA-2B33319B31DCQ39026981-05F41227-4E8E-4B7E-98D5-07B775274F02Q39504479-EECB0FC0-CAF4-4F33-B3B8-50531EED3EA3Q41019968-2334B0D7-809D-47EC-8BAF-4C25326BA4FDQ41239553-A1FCDA20-B2B1-4759-BA4F-7EB830D29998Q42429062-E2D8DB7D-73AC-470E-B27A-67078E6277A1Q43183275-0A4E621F-FE0D-48B9-AE37-13378A866272Q43575225-F23F45E3-1538-4136-9BFE-921685895A4CQ46485704-32C001EA-D573-499A-817A-B2B1CE8C8253Q46765551-57AE48A8-9983-4845-BF2B-788BDFBA3B68Q46924832-F4CF0A65-E1D5-48A0-8EE6-6F20D65E28CFQ47835763-FEA132C9-65F5-4888-934B-FCFDD4F71DC1Q47836549-A0957953-BF43-4916-8750-2913D34A5269Q48189636-D0E78AF3-693F-482D-8026-D298131B8394Q48290167-DA3DCADC-7107-467E-9D92-4333C46F6548Q48321078-C5B42F4D-6825-4812-9600-946AAA0F9B74Q49063865-D5EBB8EF-032A-4FE0-834E-EB9FF5BE016FQ50970537-D63B1B9C-788C-4F3B-9EC6-31CF1D6EA489Q51062141-9A85E4F9-6167-4273-8DB3-AA2C611A7548Q51067037-C91E8577-882B-4B41-B3AC-7DD063D9359FQ51323542-5A844D55-4F4B-4869-A854-9C1F1DB34E47Q53182089-97BFBA2D-66EA-498A-9F91-83BB2FAC4EF4Q53407404-5133E363-B8F3-4903-9D42-FFFF470B84B7Q57742468-21F252A0-5894-47DA-B6C9-488C751D3737Q57817022-E905ED55-C0BC-4FF9-9731-809A18B9F4BFQ57835125-713FC3E7-24D6-4B84-BF59-33EAF5028FF4
P2860
Highly general stereo-, regio-, and chemo-selective synthesis of terminal and internal conjugated enynes by the Pd-catalysed reaction of alkynylzinc reagents with alkenyl halides
description
wetenschappelijk artikel
@nl
наукова стаття, опублікована в 1977
@uk
name
Highly general stereo-, regio- ...... reagents with alkenyl halides
@en
Highly general stereo-, regio- ...... reagents with alkenyl halides
@nl
type
label
Highly general stereo-, regio- ...... reagents with alkenyl halides
@en
Highly general stereo-, regio- ...... reagents with alkenyl halides
@nl
prefLabel
Highly general stereo-, regio- ...... reagents with alkenyl halides
@en
Highly general stereo-, regio- ...... reagents with alkenyl halides
@nl
P2093
P356
P1476
Highly general stereo-, regio- ...... reagents with alkenyl halides
@en
P2093
Anthony O. King
Ei-ichi Negishi
Nobuhisa Okukado
P356
10.1039/C39770000683
P577
1977-01-01T00:00:00Z