On the public citation graph
Room-Temperature Stille Cross-Couplings of Alkenyltin Reagents and Functionalized Alkyl Bromides that Possess β Hydrogens
0 signed · 147 inferred · view as graph
Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.
Is this your work? Sign in with ORCID and put your name on the
claims that are yours.
Reference health. See whether every reference in this work resolves to a
known work and none has been retracted — and get a dated CiteStamped
badge you can embed.
What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/1521-3773(20020603)41:11<1945::aid-anie1945>3.0.co;2-7openalex-snapshot
A Method for Palladium-Catalyzed Cross-Couplings of Simple Alkyl Chlorides: Suzuki Reactions Catalyzed by [Pd2(dba)3]/PCy3 dba=(E,E)-dibenzylideneacetone, Cy=cyclohexyl. We thank Dr. Matthew R. Netherton for helpful discussions and Johnson Matthey Inc. for supplying palladium compounds. Support…
inferredcites →https://doi.org/10.1002/1521-3773(20020603)41:11<1947::aid-anie1947>3.0.co;2-wopenalex-snapshot
Hydrogen Bonding Modulates the Selectivity of Enzymatic Oxidation by P450: Chameleon Oxidant Behavior by Compound I The research was supported in parts by the Israel Science Foundation (ISF), the German Israeli Binational Foundation (GIF), and by the Ministry of Science, Culture, and Sports. F.O.…
inferredcites →https://doi.org/10.1002/1521-3773(20021018)41:20<3910::aid-anie3910>3.0.co;2-wopenalex-snapshot
Suzuki Cross-Couplings of Alkyl Tosylates that Possess β Hydrogen Atoms: Synthetic and Mechanistic Studies
inferredcites →https://doi.org/10.1016/s0040-4039(00)61224-8openalex-snapshot
Palladium catalyzed cross-coupling and tandem cyclization-coupling of α-halo(thio)ethers with organotins
inferredcites →https://doi.org/10.1016/s0040-4039(00)85170-9openalex-snapshot
Alkylation of aralkyl bromides with tetra alkyl tin compounds in presence of (2,2′-bipyridine)fumaronitrile palladium(0)
inferredcites →https://doi.org/10.1021/ja00042a045openalex-snapshot
Structure dependence of ammonia adsorption on alkali halide clusters
inferredcites →https://doi.org/10.1021/ja00479a077openalex-snapshot
A general, selective, and facile method for ketone synthesis from acid chlorides and organotin compounds catalyzed by palladium
inferredcites →https://doi.org/10.1021/ja00479a078openalex-snapshot
A synthesis of dl-cocaine using nitrone intermediates
inferredcites →https://doi.org/10.1021/ja011306oopenalex-snapshot
Room-Temperature Alkyl−Alkyl Suzuki Cross-Coupling of Alkyl Bromides that Possess β Hydrogens
inferredcites →https://doi.org/10.1021/ja0283899openalex-snapshot
Boronic Acids: New Coupling Partners in Room-Temperature Suzuki Reactions of Alkyl Bromides. Crystallographic Characterization of an Oxidative-Addition Adduct Generated under Remarkably Mild Conditions
inferredcites →https://doi.org/10.1021/jo00210a041openalex-snapshot
Synthesis of chrysene, 5-substituted chrysenes, and chrysene derivatives via intramolecular cycloaddition reactions
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4832801openalex-extracted
Ni@Fe3o4/L-Alanine-Acrylamide Nanocomposite Catalyzed Suzuki Transformation Reactions and Estrogen Inhibitory Activity: Experimental and Docking Investigation
inferred← citeshttps://doi.org/10.1002/047084289x.rb098s.pub2openalex-snapshot
Bis(allyl)di-μ-chlorodipalladium
inferred← citeshttps://doi.org/10.1002/047084289x.rn01701openalex-snapshot
Di-tert-butyl(methyl)phosphine
inferred← citeshttps://doi.org/10.1002/047084289x.rn01701.pub2openalex-snapshot
Di-tert-butyl(methyl)phosphine
inferred← citeshttps://doi.org/10.1002/047084289x.rn01855openalex-snapshot
Di-tert-butyl(methyl)phosphonium Tetrafluoroborate
inferred← citeshttps://doi.org/10.1002/0470862106.ia179openalex-snapshot
Palladium: Organometallic Chemistry
inferred← citeshttps://doi.org/10.1002/9780470682531.pat0374openalex-snapshot
Palladium‐ or Nickel‐Catalyzed Cross‐Coupling Reactions with Organozincs and Related Organometals
inferred← citeshttps://doi.org/10.1002/9780471264194.fos00992.pub2openalex-snapshot
Bis(allyl)dichlorodipalladium
inferred← citeshttps://doi.org/10.1002/9780471264194.fos00992.pub3openalex-snapshot
Bis(allyl)dichlorodipalladium
inferred← citeshttps://doi.org/10.1002/9781118662083.cot01-002openalex-snapshot
Formation of Alkanes and Arenes by Coupling Reactions
inferred← citeshttps://doi.org/10.1002/9781118662083.cot02-005openalex-snapshot
Formation of Alkenes by Metal‐promoted Coupling Reactions
inferred← citeshttps://doi.org/10.1002/9781119951438.eibc0165openalex-snapshot
Palladium: Organometallic Chemistry
inferred← citeshttps://doi.org/10.1002/9783527619467.ch6openalex-snapshot
Polyfunctional Tin Organometallics for Organic Synthesis
inferred← citeshttps://doi.org/10.1002/9783527619535.ch1openalex-snapshot
Mechanistic Aspects of Metal‐Catalyzed C,C‐ and C,X‐Bond‐Forming Reactions
inferred← citeshttps://doi.org/10.1002/9783527619535.ch2openalex-snapshot
Metal‐Catalyzed Cross‐Coupling Reactions of Organoboron Compounds with Organic Halides
inferred← citeshttps://doi.org/10.1002/9783527619535.ch4openalex-snapshot
Organosilicon Compounds in Cross‐Coupling Reactions
inferred← citeshttps://doi.org/10.1002/9783527655588.ch1openalex-snapshot
Mechanistic Aspects of Metal‐Catalyzed C,C‐ and C,X‐Bond Forming Reactions
inferred← citeshttps://doi.org/10.1002/9783527655588.ch6openalex-snapshot
Organotin Reagents in Cross‐Coupling Reactions
inferred← citeshttps://doi.org/10.1002/9783527655588.ch7openalex-snapshot
Organosilicon Compounds in Cross‐Coupling Reactions
inferred← citeshttps://doi.org/10.1002/9783527664801.ch16openalex-snapshot
Case Study of Mechanisms in Synthetic Reactions
inferred← citeshttps://doi.org/10.1002/9783527695959.ch1openalex-snapshot
Stille Polycondensation: A Versatile Synthetic Approach to Functional Polymers
inferred← citeshttps://doi.org/10.1002/adsc.200404223openalex-snapshot
Nickel‐Catalyzed Cross‐Couplings of Unactivated Alkyl Halides and Pseudohalides with Organometallic Compounds
inferred← citeshttps://doi.org/10.1002/adsc.201000144openalex-snapshot
Regioselective Functionalization of the Imidazole Ring via Transition Metal‐Catalyzed CN and CC Bond Forming Reactions
inferred← citeshttps://doi.org/10.1002/adsc.201200136openalex-snapshot
Alkylboronic Esters from Palladium‐ and Nickel‐Catalyzed Borylation of Primary and Secondary Alkyl Bromides
inferred← citeshttps://doi.org/10.1002/ange.200300638openalex-snapshot
Die Mechanismen der Stille‐Reaktion
inferred← citeshttps://doi.org/10.1002/ange.200352668openalex-snapshot
Ligands for Palladium‐Catalyzed Cross‐Couplings of Alkyl Halides: Use of an Alkyldiaminophosphane Expands the Scope of the Stille Reaction
inferred← citeshttps://doi.org/10.1002/ange.200352858openalex-snapshot
Toward an Improved Understanding of the Unusual Reactivity of Pd0/Trialkylphosphane Catalysts in Cross‐Couplings of Alkyl Electrophiles: Quantifying the Factors That Determine the Rate of Oxidative Addition
inferred← citeshttps://doi.org/10.1002/ange.200460246openalex-snapshot
Nickel‐Catalyzed Cross‐Coupling Reaction of Alkyl Halides with Organozinc and Grignard Reagents with 1,3,8,10‐Tetraenes as Additives
inferred← citeshttps://doi.org/10.1002/ange.200461432openalex-snapshot
Katalysatoren machen's möglich: Selektive C‐C‐Kupplungen mit nichtaktivierten Alkylhalogeniden
inferred← citeshttps://doi.org/10.1002/ange.200500918openalex-snapshot
Kupplungen von Monoorganozinn‐Verbindungen: eine “radikale” Abwandlung der ursprünglichen Stille‐Reaktion
inferred← citeshttps://doi.org/10.1002/ange.200503519openalex-snapshot
Widely Applicable Pd‐Catalyzed trans‐Selective Monoalkylation of Unactivated 1,1‐Dichloro‐1‐alkenes and Pd‐Catalyzed Second Substitution for the Selective Synthesis of E or Z Trisubstituted Alkenes
inferred← citeshttps://doi.org/10.1002/ange.201501608openalex-snapshot
Selective Formation of a Trisubstituted Alkene Motif by trans‐Hydrostannation/Stille Coupling: Application to the Total Synthesis and Late‐Stage Modification of 5,6‐Dihydrocineromycin B
inferred← citeshttps://doi.org/10.1002/anie.200300638openalex-snapshot
The Mechanisms of the Stille Reaction
inferred← citeshttps://doi.org/10.1002/anie.200352668openalex-snapshot
Ligands for Palladium‐Catalyzed Cross‐Couplings of Alkyl Halides: Use of an Alkyldiaminophosphane Expands the Scope of the Stille Reaction
inferred← citeshttps://doi.org/10.1002/anie.200352858openalex-snapshot
Toward an Improved Understanding of the Unusual Reactivity of Pd0/Trialkylphosphane Catalysts in Cross‐Couplings of Alkyl Electrophiles: Quantifying the Factors That Determine the Rate of Oxidative Addition
inferred← citeshttps://doi.org/10.1002/anie.200460246openalex-snapshot
Nickel‐Catalyzed Cross‐Coupling Reaction of Alkyl Halides with Organozinc and Grignard Reagents with 1,3,8,10‐Tetraenes as Additives
inferred← citeshttps://doi.org/10.1002/anie.200461432openalex-snapshot
Catalysts for Cross‐Coupling Reactions with Non‐activated Alkyl Halides
inferred← citeshttps://doi.org/10.1002/anie.200500918openalex-snapshot
Couplings with Monoorganotin Compounds: A “Radical” Twist from the Original Stille Reaction
inferred← citeshttps://doi.org/10.1002/anie.200503519openalex-snapshot
Widely Applicable Pd‐Catalyzed trans‐Selective Monoalkylation of Unactivated 1,1‐Dichloro‐1‐alkenes and Pd‐Catalyzed Second Substitution for the Selective Synthesis of E or Z Trisubstituted Alkenes
inferred← citeshttps://doi.org/10.1002/anie.201501608openalex-snapshot
Selective Formation of a Trisubstituted Alkene Motif by trans‐Hydrostannation/Stille Coupling: Application to the Total Synthesis and Late‐Stage Modification of 5,6‐Dihydrocineromycin B
inferred← citeshttps://doi.org/10.1002/aoc.1263openalex-snapshot
First 1,1‐organoboration reactions of vinyltin compounds—a route to boryl‐substituted stannolanes and organo‐substituted stannol‐3‐enes
inferred← citeshttps://doi.org/10.1002/chem.200305667openalex-snapshot
Chiral Nonracemic Late‐Transition‐Metal Organometallics with a Metal‐Bonded Stereogenic Carbon Atom: Development of New Tools for Asymmetric Organic Synthesis
inferred← citeshttps://doi.org/10.1002/chem.200400545openalex-snapshot
Cobalt‐Catalyzed Cross‐Coupling Reactions of Alkyl Halides with Allylic and Benzylic Grignard Reagents and Their Application to Tandem Radical Cyclization/Cross‐Coupling Reactions
inferred← citeshttps://doi.org/10.1002/chem.200601142openalex-snapshot
9‐Fluorenylphosphines for the Pd‐Catalyzed Sonogashira, Suzuki, and Buchwald–Hartwig Coupling Reactions in Organic Solvents and Water
inferred← citeshttps://doi.org/10.1002/chem.200800423openalex-snapshot
When Are Tricoordinated Pd II Species Accessible? Stability Trends and Mechanistic Consequences
inferred← citeshttps://doi.org/10.1002/chem.200902842openalex-snapshot
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
inferred← citeshttps://doi.org/10.1002/chem.201001631openalex-snapshot
Palladium‐ and Nickel‐Catalyzed Direct Alkylation of Azoles with Unactivated Alkyl Bromides and Chlorides
inferred← citeshttps://doi.org/10.1002/chem.201103882openalex-snapshot
Theoretical Study on the Mechanism of Ni‐Catalyzed Alkyl–Alkyl Suzuki Cross‐Coupling
inferred← citeshttps://doi.org/10.1002/chem.201301937openalex-snapshot
Oxidative Addition to Palladium(0) Diphosphine Complexes: Observations of Mechanistic Complexity with Iodobenzene as Reactant
inferred← citeshttps://doi.org/10.1002/chem.201403093openalex-snapshot
Palladium‐Catalyzed Intramolecular Reductive Cross‐Coupling of Csp2Csp3 Bond Formation
inferred← citeshttps://doi.org/10.1002/chem.201500774openalex-snapshot
Palladium‐Catalyzed [3+3] Annulation between Diarylamines and α,β‐Unsaturated Acids through CH Activation: Direct Access to 4‐Substituted 2‐Quinolinones
inferred← citeshttps://doi.org/10.1002/chem.201501208openalex-snapshot
Divergent Reactivity in Palladium‐Catalyzed Annulation with Diarylamines and α,β‐Unsaturated Acids: Direct Access to Substituted 2‐Quinolinones and Indoles
inferred← citeshttps://doi.org/10.1002/chem.201702470openalex-snapshot
Two Enabling Strategies for the Stereoselective Conversion of Internal Alkynes into Trisubstituted Alkenes
inferred← citeshttps://doi.org/10.1002/chin.200332049openalex-snapshot
Room‐Temperature Stille Cross‐Couplings of Alkenyltin Reagents and Functionalized Alkyl Bromides that Possess β Hydrogens.
inferred← citeshttps://doi.org/10.1002/jccs.200400155openalex-snapshot
Efficient Coupling of Allylstannane with Diels‐Alder Cycloadducts Derived from 4‐Bromo‐substituted Masked o‐Benzoquinones: Synthesis of 5‐Allyl‐oxatricyclo[m.3.1.0]decenones and Undecenones
inferred← citeshttps://doi.org/10.1002/tcr.201400002openalex-snapshot
Pd0‐Mediated Rapid Cross‐Coupling Reactions, the Rapid C‐[11C]Methylations, Revolutionarily Advancing the Syntheses of Short‐Lived PET Molecular Probes
inferred← citeshttps://doi.org/10.1007/s00214-009-0539-7openalex-snapshot
The role of amide ligands in the stabilization of Pd(II) tricoordinated complexes: is the Pd–NR2 bond order single or higher?
inferred← citeshttps://doi.org/10.1007/s11244-005-3814-4openalex-snapshot
Control of the β-Hydride Elimination Making Palladium-Catalyzed Coupling Reactions more Diversified
inferred← citeshttps://doi.org/10.1016/b0-08-044655-8/00011-8openalex-snapshot
One or More CC Bond(s) Formed by Substitution or Addition
inferred← citeshttps://doi.org/10.1016/b0-08-045047-4/00143-6openalex-snapshot
C–C Bond Formation by Cross-coupling
inferred← citeshttps://doi.org/10.1016/b978-0-08-097742-3.00312-8openalex-snapshot
3.08 Coupling Reactions Between sp3 and sp2 Carbon Centers
inferred← citeshttps://doi.org/10.1016/b978-0-08-097774-4.00603-3openalex-snapshot
Cross-Coupling Reactions
inferred← citeshttps://doi.org/10.1016/b978-0-12-409547-2.03966-4openalex-snapshot
C–C Bond Formation by Cross-Coupling
inferred← citeshttps://doi.org/10.1016/b978-0-323-96025-0.00070-3openalex-snapshot
Coupling Reactions Between sp3 and sp2 Carbon Centers
inferred← citeshttps://doi.org/10.1016/j.bmc.2008.04.017openalex-snapshot
Synthesis of 5′-functionalized nucleosides: S-Adenosylhomocysteine analogues with the carbon-5′ and sulfur atoms replaced by a vinyl or halovinyl unit
inferred← citeshttps://doi.org/10.1016/j.ccr.2005.03.033openalex-snapshot
Transition metals in organic synthesis: Highlights for the year 2003
inferred← citeshttps://doi.org/10.1016/j.ccr.2007.12.025openalex-snapshot
Transition metal-dialkyl compounds (LxMR2; R=alkyl; M=metals of groups VI–X)—Synthesis, structure, reactivity and applications
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2009.06.035openalex-snapshot
Perfluoroalkylphosphines and arsines obtained by Pd-catalyzed cross-coupling reaction with organoheteroatom stannanes
inferred← citeshttps://doi.org/10.1016/j.poly.2025.117495openalex-snapshot
Ni@Fe3O4/l-alanine-acrylamide nanocomposite catalyzed Suzuki transformation reactions and estrogen inhibitory activity: Experimental and docking investigation
inferred← citeshttps://doi.org/10.1016/j.steroids.2012.01.003openalex-snapshot
Synthesis and evaluation of 17α-(dimethylphenyl)vinyl estradiols as probes of the estrogen receptor-α ligand binding domain
inferred← citeshttps://doi.org/10.1016/j.tet.2005.04.073openalex-snapshot
An efficient Stille cross-coupling reaction catalyzed by Pd(OAc)2/DAB-Cy catalytic system
inferred← citeshttps://doi.org/10.1016/j.tet.2005.07.101openalex-snapshot
Towards the rational design of palladium-N-heterocyclic carbene catalysts by a combined experimental and computational approach
inferred← citeshttps://doi.org/10.1016/j.tet.2010.05.026openalex-snapshot
Pyrazole-tethered phosphine ligands for Pd(0): useful catalysts for Stille, Kumada and Hiyama cross-coupling reactions
inferred← citeshttps://doi.org/10.1016/j.tet.2010.06.019openalex-snapshot
Regioselective control using a catalyst switch in the reaction of diarylmethyl chlorides with allyltributylstannane
inferred← citeshttps://doi.org/10.1016/j.tet.2015.10.069openalex-snapshot
Newly-generated Al(OH) 3 -supported Pd nanoparticles-catalyzed Stille and Kumada coupling reactions of diazonium salts, (Het)aryl chlorides
inferred← citeshttps://doi.org/10.1016/j.trac.2004.06.003openalex-snapshot
Rapid methylation on carbon frameworks leading to the synthesis of a PET tracer capable of imaging a novel CNS-type prostacyclin receptor in living human brain
inferred← citeshttps://doi.org/10.1021/acs.organomet.9b00409openalex-snapshot
C(sp3)–Cl Bond Activation Promoted by a POP-Pincer Rhodium(I) Complex
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c01557openalex-snapshot
Cobalt-Bisoxazoline-Catalyzed Enantioselective Cross-Coupling of α-Bromo Esters with Alkenyl Grignard Reagents
inferred← citeshttps://doi.org/10.1021/acs.orglett.6c03404openalex-snapshot
Palladium-Catalyzed Enantioselective Dearomative Domino Heck/Stille Reaction of Indoles
inferred← citeshttps://doi.org/10.1021/acsomega.0c04874openalex-snapshot
Synthesis of Benzyl 2-Deoxy- C -Glycosides
inferred← citeshttps://doi.org/10.1021/cr100320wopenalex-snapshot
Stille Polycondensation for Synthesis of Functional Materials
inferred← citeshttps://doi.org/10.1021/ja031766copenalex-snapshot
Efficient Stereoselective Alkenylation through a Homolytic Domino Reaction Involving a 1,5 Sulfur-to-Carbon Translocation
inferred← citeshttps://doi.org/10.1021/ja0349352openalex-snapshot
Room-Temperature Hiyama Cross-Couplings of Arylsilanes with Alkyl Bromides and Iodides
inferred← citeshttps://doi.org/10.1021/ja036290bopenalex-snapshot
Decarbonylative Cross-Coupling of Cyclic Anhydrides: Introducing Stereochemistry at an sp3 Carbon in the Cross-Coupling Event
inferred← citeshttps://doi.org/10.1021/ja0363258openalex-snapshot
Palladium-Catalyzed Negishi Cross-Coupling Reactions of Unactivated Alkyl Iodides, Bromides, Chlorides, and Tosylates
inferred← citeshttps://doi.org/10.1021/ja038177ropenalex-snapshot
The First Applications of Carbene Ligands in Cross-Couplings of Alkyl Electrophiles: Sonogashira Reactions of Unactivated Alkyl Bromides and Iodides
inferred← citeshttps://doi.org/10.1021/ja0393729openalex-snapshot
Cross-Couplings of Alkyl Electrophiles under “Ligandless” Conditions: Negishi Reactions of Organozirconium Reagents
inferred← citeshttps://doi.org/10.1021/ja039889kopenalex-snapshot
Suzuki Cross-Couplings of Unactivated Secondary Alkyl Bromides and Iodides
inferred← citeshttps://doi.org/10.1021/ja042479ropenalex-snapshot
Dendrimer-Encapsulated Pd Nanoparticles as Aqueous, Room-Temperature Catalysts for the Stille Reaction
inferred← citeshttps://doi.org/10.1021/ja054779uopenalex-snapshot
Changes in Coordination of Sterically Demanding Hybrid Imidazolylphosphine Ligands on Pd(0) and Pd(II)
inferred← citeshttps://doi.org/10.1021/ja0647351openalex-snapshot
Oxidative Cross-Coupling through Double Transmetallation: Surprisingly High Selectivity for Palladium-Catalyzed Cross-Coupling of Alkylzinc and Alkynylstannanes
inferred← citeshttps://doi.org/10.1021/ja204080sopenalex-snapshot
Anti-Markovnikov Hydroalkylation of Allylic Amine Derivatives via a Palladium-Catalyzed Reductive Cross-Coupling Reaction
inferred← citeshttps://doi.org/10.1021/ja3113752openalex-snapshot
Palladium-Catalyzed C–H Activation/Cross-Coupling of Pyridine N-Oxides with Nonactivated Secondary Alkyl Bromides
inferred← citeshttps://doi.org/10.1021/ja9027378openalex-snapshot
Functional Group Tolerant Kumada−Corriu−Tamao Coupling of Nonactivated Alkyl Halides with Aryl and Heteroaryl Nucleophiles: Catalysis by a Nickel Pincer Complex Permits the Coupling of Functionalized Grignard Reagents
inferred← citeshttps://doi.org/10.1021/jacs.3c00885openalex-snapshot
Tris(bicyclo[1.1.1]pentyl)phosphine: An Exceptionally Small Tri-tert-alkylphosphine and Its Bis-Ligated Pd(0) Complex
inferred← citeshttps://doi.org/10.1021/jo047773gopenalex-snapshot
Application of Vinyl Tris(trimethylsilyl)germanes in Pd-Catalyzed Couplings
inferred← citeshttps://doi.org/10.1021/jo047907qopenalex-snapshot
Stille Cross-Coupling of Activated Alkyltin Reagents under “Ligandless” Conditions
inferred← citeshttps://doi.org/10.1021/jo051304copenalex-snapshot
Room-Temperature Negishi Cross-Coupling of Unactivated Alkyl Bromides with Alkyl Organozinc Reagents Utilizing a Pd/N-Heterocyclic Carbene Catalyst
inferred← citeshttps://doi.org/10.1021/jo051980eopenalex-snapshot
Synthesis of the Multisubstituted Halogenated Olefins via Cross-Coupling of Dihaloalkenes with Alkylzinc Bromides
inferred← citeshttps://doi.org/10.1021/jo0600353openalex-snapshot
Synthesis of a Sterically Crowded Atropisomeric 1,8-Diacridylnaphthalene for Dual-Mode Enantioselective Fluorosensing
inferred← citeshttps://doi.org/10.1021/jo802082topenalex-snapshot
A Short Entry to α-Substituted γ-Alkylidene Pentenolides. Synthesis and Preliminary Biological Evaluation of Novel Gelastatin Analogues
inferred← citeshttps://doi.org/10.1021/ol035802oopenalex-snapshot
Nickel-Catalyzed Olefination of Unactivated Aliphatic Dithioacetals
inferred← citeshttps://doi.org/10.1021/ol049312nopenalex-snapshot
Radical-Mediated Silyl- and Germyldesulfonylation of Vinyl and (α-Fluoro)vinyl Sulfones: Application of Tris(trimethylsilyl)silanes and Tris(trimethylsilyl)germanes in Pd-Catalyzed Couplings
inferred← citeshttps://doi.org/10.1021/ol049686gopenalex-snapshot
Kumada−Corriu Reactions of Alkyl Halides with Alkynyl Nucleophiles
inferred← citeshttps://doi.org/10.1021/ol049779yopenalex-snapshot
Iron-Catalyzed Grignard Cross-Coupling with Alkyl Halides Possessing β-Hydrogens
inferred← citeshttps://doi.org/10.1021/ol052579hopenalex-snapshot
Phosphorinanes as Ligands for Palladium-Catalyzed Cross-Coupling Chemistry
inferred← citeshttps://doi.org/10.1021/ol101995vopenalex-snapshot
Rhodium-Catalyzed Activation of C(sp 3 )−X (X = Cl, Br) Bond: An Intermolecular Halogen Exchange Case
inferred← citeshttps://doi.org/10.1021/ol303129popenalex-snapshot
The Palladium-Catalyzed Anti-Markovnikov Hydroalkylation of Allylic Alcohol Derivatives
inferred← citeshttps://doi.org/10.1021/ol500408aopenalex-snapshot
Stereospecific Ni-Catalyzed Cross-Coupling of Potassium Alkenyltrifluoroborates with Alkyl Halides
inferred← citeshttps://doi.org/10.1021/om070094mopenalex-snapshot
1-Indenyldialkylphosphines and Cyclopentadienyldialkylphosphines as Ligands for High-Activity Palladium-Catalyzed Cross-Coupling Reactions with Aryl Chlorides
inferred← citeshttps://doi.org/10.1021/om2006936openalex-snapshot
Characterization, Reactivity, and Potential Catalytic Intermediacy of a Cyclometalated Tri-tert-butylphosphine Palladium Acetate Complex
inferred← citeshttps://doi.org/10.1021/om300455gopenalex-snapshot
Computational Mechanistic Study of Stereoselective Suzuki Coupling of an α-Cyano-Activated Secondary Alkyl
inferred← citeshttps://doi.org/10.1021/om3011992openalex-snapshot
Electron-Rich Trialkyl-Type Dihydro-KITPHOS Monophosphines: Efficient Ligands for Palladium-Catalyzed Suzuki–Miyaura Cross-Coupling. Comparison with Their Biaryl-Like KITPHOS Monophosphine Counterparts
inferred← citeshttps://doi.org/10.1021/om400144sopenalex-snapshot
A Chiral Bis(arsine) Ligand: Synthesis and Applications in Palladium-Catalyzed Asymmetric Allylic Alkylations
inferred← citeshttps://doi.org/10.1021/om900732copenalex-snapshot
Highly Efficient Palladium-Catalyzed Arsination. Synthesis of a Biphenyl Arsine Ligand and Its Application to Obtain Perfluoroalkylarsines
inferred← citeshttps://doi.org/10.1039/b311532aopenalex-snapshot
Rapid methylation of terminal acetylenes by the Stille coupling of methyl iodide with alkynyltributylstannanes: a general protocol potentially useful for the synthesis of short-lived 11CH3-labeled PET tracers with a 1-propynyl groupElectronic supplementary information (ESI) available: general…
inferred← citeshttps://doi.org/10.1039/b402096kopenalex-snapshot
5 Transition metals in organic synthesis
inferred← citeshttps://doi.org/10.1039/b515215aopenalex-snapshot
Rapid methylation on carbon frameworks useful for the synthesis of 11CH3-incorporated PET tracers: Pd(0)-mediated rapid coupling of methyl iodide with an alkenyltributylstannane leading to a 1-methylalkene
inferred← citeshttps://doi.org/10.1039/c1cs15129kopenalex-snapshot
Pd-catalyzed cross-coupling reactions of alkyl halides
inferred← citeshttps://doi.org/10.1039/c2cc33294aopenalex-snapshot
Ligand effects on the stereochemistry of Stille couplings, as manifested in reactions of Z-alkenyl halides
inferred← citeshttps://doi.org/10.1039/c3ra40815aopenalex-snapshot
Pd 0 -mediated rapid coupling of methyl iodide with excess amounts of benzyl- and cinnamylboronic acid esters: efficient method for incorporation of positron-emitting 11 C radionuclide into organic frameworks by coupling between two sp 3 -hybridized carbons
inferred← citeshttps://doi.org/10.1039/c4cc09810bopenalex-snapshot
AsCat and FurCat: new Pd catalysts for selective room-temperature Stille cross-couplings of benzyl chlorides with organostannanes
inferred← citeshttps://doi.org/10.1039/c5qo00091bopenalex-snapshot
Pd-catalyzed Heck cyclization and in situ hydrocarboxylation or hydromethenylation via a hydrogen borrowing strategy
inferred← citeshttps://doi.org/10.1039/c5ra09960aopenalex-snapshot
Carbastannatranes: a powerful coupling mediators in Stille coupling
inferred← citeshttps://doi.org/10.1039/d2nj04270copenalex-snapshot
Synthesis, coordination behavior, and catalytic properties of dppf congeners with an inserted carbonyl moiety
inferred← citeshttps://doi.org/10.1055/sos-sd-239-00056openalex-snapshot
2.1 Base-Metal-Mediated Cross Couplings Using N-(Acyloxy)phthalimides
inferred← citeshttps://doi.org/10.1139/v2012-044openalex-snapshot
Diphenylphosphinoethane-functionalized polystyrene resin-supported Pd(0) complex — A highly active and recyclable catalyst for the Stille reaction under aerobic conditions
inferred← citeshttps://doi.org/10.1246/bcsj.80.233openalex-snapshot
Transition Metal-Catalyzed Organometallic Reactions that Have Revolutionized Organic Synthesis
inferred← citeshttps://doi.org/10.1246/cl.2003.890openalex-snapshot
Pd-Catalyzed Cross-Coupling Reaction of Alkyl Tosylates and Bromides with Grignard Reagents in the Presence of 1,3-Butadiene
inferred← citeshttps://doi.org/10.2174/1385272824666200211114540openalex-snapshot
Monodentate Trialkylphosphines: Privileged Ligands in Metal-catalyzed Crosscoupling Reactions
inferred← citeshttps://doi.org/10.5059/yukigoseikyokaishi.68.1195openalex-snapshot
Pd0-Mediated Rapid C-[11C]Methylations and C-[18F]Fluoromethylations: Revolutionary New Methodologies for the Synthesis of Short-Lived PET Molecular Probes
inferred← citeshttps://doi.org/10.5059/yukigoseikyokaishi.74.792openalex-snapshot
Highly Selective Synthesis of Multi-substituted Olefins Mediated by Zirconocene Complexes
inferred← citeshttps://doi.org/10.5772/intechopen.70746openalex-snapshot
Green Process of Three-Component Prostaglandin Synthesis and Rapid 11C Labelings for Short-Lived PET Tracers
inferred← citeshttps://doi.org/10.5772/intechopen.72868openalex-snapshot
Green Process of Three-Component Prostaglandin Synthesis and Rapid 11C Labelings for Short-Lived PET Tracers
inferred← citeshttps://doi.org/10.70675/769128d4ze3b5z4820z8adaz6a70ca268212openalex-snapshot
Elaboration of functional copolymers absorbing in the near infrared region
Editorial review for independent work. ICSAC — the Institute for Complexity
Science and Advanced Computing — runs a structured editorial panel for researchers
publishing outside journals, and publishes on CiteStamp rails. Submission is free
and goes through ORCID: icsacinstitute.org/submit.