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Utilization of Sequential Palladium-Catalyzed Cross-Coupling Reactions in the Stereospecific Synthesis of Trisubstituted Olefins
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/9783527612222.ch5openalex-snapshot
Cross‐Coupling Reactions to sp Carbon Atoms
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The Directed ortho‐Metallation (DoM) Cross‐Coupling Nexus. Synthetic Methodology for the Formation of Aryl‐Aryl and Aryl‐Heteroatom‐Aryl Bonds
inferredcites →https://doi.org/10.1002/anie.200300590openalex-snapshot
Beyond Thermodynamic Acidity: A Perspective on the Complex‐Induced Proximity Effect (CIPE) in Deprotonation Reactions
inferredcites →https://doi.org/10.1002/anie.200600012openalex-snapshot
Stereoselective Synthesis of the Side Chains of Mycolactones A and B Featuring Stepwise Double Substitutions of 1,1‐Dibromo‐1‐alkenes
inferredcites →https://doi.org/10.1002/anie.200600025openalex-snapshot
Palladium‐Catalyzed Coupling Reactions for the Stereoselective Synthesis of Tri‐ and Tetrasubstituted Alkenes
inferredcites →https://doi.org/10.1002/chem.200600206openalex-snapshot
A User‐Friendly, All‐Purpose Pd–NHC (NHC=N‐Heterocyclic Carbene) Precatalyst for the Negishi Reaction: A Step Towards a Universal Cross‐Coupling Catalyst
inferredcites →https://doi.org/10.1002/chem.200600251openalex-snapshot
Easily Prepared Air‐ and Moisture‐Stable Pd–NHC (NHC=N‐Heterocyclic Carbene) Complexes: A Reliable, User‐Friendly, Highly Active Palladium Precatalyst for the Suzuki–Miyaura Reaction
inferredcites →https://doi.org/10.1016/s0022-328x(00)92296-4openalex-snapshot
Application of hydroalumination reactions in organic syntheses. coupling reactions of organoaluminum compounds with allylic halides catalyzed by copper compounds
inferredcites →https://doi.org/10.1016/s0040-4039(00)78081-6openalex-snapshot
A stereoselective synthesis of disubstituted trans-alkenes by the reaction of trans-alkenyl trialkylaluminates with alkyl halides and sulfonates
inferredcites →https://doi.org/10.1016/s0040-4039(00)78541-8openalex-snapshot
Synthesis of functionalized furo[2,3-b]pyridines via the Pd-catalyzed coupling of acetylenes to iodopyridones. Preparation of a key intermediate to a new HIV protease inhibitor L-754,394
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Alkylation of 1-trimethylsilylvinyl aluminates with “unreactive” alkyl halides mediated by cuprous iodide-trimethyl phosphite complex
inferredcites →https://doi.org/10.1021/cr00020a002openalex-snapshot
Substrate-directable chemical reactions
inferredcites →https://doi.org/10.1021/ja01022a060openalex-snapshot
Stereospecific total synthesis of the dl-C18 Cecropia juvenile hormone
inferredcites →https://doi.org/10.1021/ja028865vopenalex-snapshot
Copper-Catalyzed Halogen Exchange in Aryl Halides: An Aromatic Finkelstein Reaction
inferredcites →https://doi.org/10.1021/ja057704zopenalex-snapshot
Modified (NHC)Pd(allyl)Cl (NHC = N-Heterocyclic Carbene) Complexes for Room-Temperature Suzuki−Miyaura and Buchwald−Hartwig Reactions
inferredcites →https://doi.org/10.1021/ja0772039openalex-snapshot
Highly Stereo- and Regioselective Synthesis of (Z)-Trisubstituted Alkenes via 1-Bromo-1-alkyne Hydroboration−Migratory Insertion−Zn-Promoted Iodinolysis and Pd-Catalyzed Organozinc Cross-Coupling
inferredcites →https://doi.org/10.1021/ja990432dopenalex-snapshot
Nickel on Charcoal (“Ni/C”): An Expedient and Inexpensive Heterogeneous Catalyst for Cross-Couplings between Aryl Chlorides and Organometallics. I. Functionalized Organozinc Reagents
inferredcites →https://doi.org/10.1021/jo0162235openalex-snapshot
3,3-Disubstituted Allyl Alcohols from Palladium-Catalyzed Coupling of Hydroaluminated Propargyl Alcohols with Aryl Iodides
inferredcites →https://doi.org/10.1021/jo048066qopenalex-snapshot
Efficient Stille Cross-Coupling Reaction Catalyzed by the Pd(OAc)2/Dabco Catalytic System
inferredcites →https://doi.org/10.1021/ol0058947openalex-snapshot
Pd(PhCN)2Cl2/P(t-Bu)3: A Versatile Catalyst for Sonogashira Reactions of Aryl Bromides at Room Temperature
inferredcites →https://doi.org/10.1021/ol0613721openalex-snapshot
trans-Hydroalumination/Alkylation: One-Pot Synthesis of Trisubstituted Allylic Alcohols
inferredcites →https://doi.org/10.1021/om011021kopenalex-snapshot
Efficient Sonogashira Reactions of Aryl Bromides with Alkynylsilanes Catalyzed by a Palladium/Imidazolium Salt System
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Sunlight Induced C-H Arylation of Aromatic Heterocycles First Example of A3 and A2b Type Corroles as Photoredox Catalysts
inferred← citeshttps://doi.org/10.1002/0471264180.or116.01openalex-snapshot
A Half Century of the Sonogashira Reaction
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Selected Applications of Transition Metal‐Catalyzed Carbon–Carbon Cross‐Coupling Reactions in the Pharmaceutical Industry
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Palladium‐Catalyzed Cross‐Coupling Reactions – Industrial Applications
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Large‐Scale Applications of Transition Metal Removal Techniques in the Manufacture of Pharmaceuticals
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Catalytic Cross‐Coupling Reactions – Nobel Prize Catalysis
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Highly Dispersed Palladium–Polypyrrole Nanocomposites: In‐Water Synthesis and Application for Catalytic Arylation of Heteroaromatics by Direct C–H Bond Activation
inferred← citeshttps://doi.org/10.1002/adsc.201400754openalex-snapshot
Removal of Palladium from Cross‐Coupling Reactions Using Isocyanide Reagents
inferred← citeshttps://doi.org/10.1002/ange.201002987openalex-snapshot
A Versatile Palladium/Triphosphane System for Direct Arylation of Heteroarenes with Chloroarenes at Low Catalyst Loading
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Die Entwicklung raumerfüllender Palladium‐NHC‐Komplexe für anspruchsvollste Kreuzkupplungsreaktionen
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Auf dem Weg zu “grüneren” übergangsmetallkatalysierten Verfahren: Quantifizierung durch den E‐Faktor
inferred← citeshttps://doi.org/10.1002/ange.201803472openalex-snapshot
Remote Central‐to‐Axial Chirality Conversion: Direct Atroposelective Ester to Biaryl Transformation
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Mild and Robust Stille Reactions in Water using Parts Per Million Levels of a Triphenylphosphine‐Based Palladacycle
inferred← citeshttps://doi.org/10.1002/anie.201002987openalex-snapshot
A Versatile Palladium/Triphosphane System for Direct Arylation of Heteroarenes with Chloroarenes at Low Catalyst Loading
inferred← citeshttps://doi.org/10.1002/anie.201106131openalex-snapshot
The Development of Bulky Palladium NHC Complexes for the Most‐Challenging Cross‐Coupling Reactions
inferred← citeshttps://doi.org/10.1002/anie.201302020openalex-snapshot
On the Way Towards Greener Transition‐Metal‐Catalyzed Processes as Quantified by E Factors
inferred← citeshttps://doi.org/10.1002/anie.201803472openalex-snapshot
Remote Central‐to‐Axial Chirality Conversion: Direct Atroposelective Ester to Biaryl Transformation
inferred← citeshttps://doi.org/10.1002/anie.202014141openalex-snapshot
Mild and Robust Stille Reactions in Water using Parts Per Million Levels of a Triphenylphosphine‐Based Palladacycle
inferred← citeshttps://doi.org/10.1002/chin.201023203openalex-snapshot
ChemInform Abstract: Practical Aspects of Carbon—Carbon Cross‐Coupling Reactions Using Heteroarenes
inferred← citeshttps://doi.org/10.1007/3418_2011_26openalex-snapshot
Case Study: Sequential Pd-Catalyzed Cross-Coupling Reactions; Challenges on Scale-Up
inferred← citeshttps://doi.org/10.1016/b978-0-08-095167-6.00909-5openalex-snapshot
9.9 Catalyst Recovery and Recycle: Metal Removal Techniques
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8.24 Hydrometallation of CC and CC Bonds. Group 3
inferred← citeshttps://doi.org/10.1016/b978-0-12-801457-8.00012-4openalex-snapshot
Use of Catalysis for API Manufacturing
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Sunlight induced C-H arylation of aromatic heterocycles: First example of A3 and A2B type corroles as photoredox catalysts
inferred← citeshttps://doi.org/10.1016/j.tet.2011.11.002openalex-snapshot
Palladium(II)-catalyzed enyne cyclization strategies toward the podophyllotoxin ring system
inferred← citeshttps://doi.org/10.1021/acs.oprd.1c00041openalex-snapshot
Heterogeneous Catalysis for Cross-Coupling Reactions: An Underutilized Powerful and Sustainable Tool in the Fine Chemical Industry?
inferred← citeshttps://doi.org/10.1021/acs.oprd.1c00180openalex-snapshot
Thermal Hazards of Using Propargyl Alcohol with Strong Bases
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Palladium Extraction Following Metal-Catalyzed Reactions: Recent Advances and Applications in the Pharmaceutical Industry
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SDMA (Synhydrid, Red-Al, Vitride): A Chemoselective and Safe Solution for Reduction Reactions
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Development of a Scalable Synthesis for the Potent Kinase Inhibitor BMS-986236; 1-(5-(4-(3-Hydroxy-3-methylbutyl)-1H-1,2,3-triazol-1-yl)-4-(isopropylamino)pyridin-2-yl)-1H-pyrazolo[3,4-b]pyridine-5-carbonitrile
inferred← citeshttps://doi.org/10.1021/acs.oprd.9b00126openalex-snapshot
Mizoroki–Heck Cross-Coupling of Bromobenzenes with Styrenes: Another Example of Pd-Catalyzed Cross-Coupling with Potential Safety Hazards
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Potential Safety Hazards Associated with Pd-Catalyzed Cross-Coupling Reactions
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One-Pot Synthesis of α,β-Unsaturated γ-Lactones and Lactams via a Sequential trans-Hydroalumination and Catalytic Carboxylation of Propargyl Alcohols and Amines with Carbon Dioxide
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Large-Scale Applications of Transition Metal-Catalyzed Couplings for the Synthesis of Pharmaceuticals
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Unsymmetric Electronic Push−Pull Bipyrroles − Synthesis, Spectroelectrochemical, and Photophysical Investigation
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Toxicological Assessment of 2-Methyltetrahydrofuran and Cyclopentyl Methyl Ether in Support of Their Use in Pharmaceutical Chemical Process Development
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Efficient Screening and Library Generation in Parallel C–C Coupling Reactions Mediated by Organosilica SiliaCat Palladium Catalysts
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Sonogashira Reactions with Propyne: Facile Synthesis of 4-Hydroxy-2-methylbenzofurans from Iodoresorcinols
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Synthesis of alkynyl/alkenyl-substituted pyridine derivatives via heterocyclization and Pd-mediated Sonogashira/Heck coupling process in one-pot: a new MCR strategy
inferred← citeshttps://doi.org/10.1039/c7gc01765kopenalex-snapshot
Potassium isopropyl xanthate (PIX): an ultra-efficient palladium scavenger
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Green Solvents for Eco-Friendly Synthesis of Dimethindene: A Forward-Looking Approach
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Complexes de nickel caméléons : exploration de tous ses degrès d'oxydation pour la formation de liaisons C-C et C-CF3
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