Every reference with a DOI in the deposited reference list resolved to a known
work in Crossref or DataCite at the dated check, and none carried a retraction,
withdrawal, or removal notice.
The 96 checked references that resolve
resolves10.1021/cr020027wAsymmetric Transition-Metal-Catalyzed Allylic Alkylations: Applications in Total Synthesis
resolves10.1021/cr300389uLate Transition Metal-Catalyzed Hydroamination and Hydroamidation
resolves10.1021/cr0306788Hydroamination: Direct Addition of Amines to Alkenes and Alkynes
resolves10.1039/C5CS00144GTransition metal-catalyzed allylic substitution reactions with unactivated allylic substrates
resolves10.1039/c0sc00234hCatalytic asymmetric allylic alkylation employing heteroatom nucleophiles: a powerful method for C–X bond formation
resolves10.1021/ol050029dEffects of Catalyst Activation and Ligand Steric Properties on the Enantioselective Allylation of Amines and Phenoxides
resolves10.1021/jo980209jPalladium(0)-Catalyzed Allylation of Highly Acidic and Nonnucleophilic Anilines. The Origin of Stereochemical Scrambling When Using Allylic Carbonates
resolves10.1021/ja054331tA Simple Iridium Catalyst with a Single Resolved Stereocenter for Enantioselective Allylic Amination. Catalyst Selection from Mechanistic Analysis
resolves10.1021/ja0644273Sequential Catalytic Isomerization and Allylic Substitution. Conversion of Racemic Branched Allylic Carbonates to Enantioenriched Allylic Substitution Products
resolves10.1002/anie.201106737Platinum‐Catalyzed Direct Amination of Allylic Alcohols with Aqueous Ammonia: Selective Synthesis of Primary Allylamines
resolves10.1002/cssc.201300723Hydrogen‐Bond‐Assisted Activation of Allylic Alcohols for Palladium‐Catalyzed Coupling Reactions
resolves10.1021/om000997eRegio- and Stereoselectivity in Palladium(0)-Catalyzed Allylation of Anilines Using Allylic Alcohols Directly
resolves10.1021/ol048207aWater Enables Direct Use of Allyl Alcohol for Tsuji−Trost Reaction without Activators
resolves10.1021/ja9046075Platinum-Catalyzed Direct Amination of Allylic Alcohols under Mild Conditions: Ligand and Microwave Effects, Substrate Scope, and Mechanistic Study
resolves10.1021/ol070890oEffective Monoallylation of Anilines Catalyzed by Supported KF
resolves10.1021/jo3025253Achieving Control over the Branched/Linear Selectivity in Palladium-Catalyzed Allylic Amination
resolves10.1021/jo9003037Palladium Nanoparticle-Catalyzed C−N Bond Formation. A Highly Regio- and Stereoselective Allylic Amination by Allyl Acetates
resolves10.1002/anie.201308874A General Catalytic Hydroamidation of 1,3‐Dienes: Atom‐Efficient Synthesis of <i>N</i>‐Allyl Heterocycles, Amides, and Sulfonamides
resolves10.1039/c4qo00023dPalladium-catalysed regioselective hydroamination of 1,3-dienes: synthesis of allylic amines
resolves10.1021/ol050524+Ruthenium-Catalyzed Intermolecular Coupling Reactions of Arylamines with Ethylene and 1,3-Dienes: Mechanistic Insight on Hydroamination vs <i>o</i><i>rtho</i>-C−H Bond Activation
resolves10.1002/1521-3773(20011203)40:23<4501::AID-ANIE4501>3.0.CO;2-K(η3-Allyl)palladium Complexes Bearing Diphosphinidenecyclobutene Ligands: Highly Active Catalysts for the Hydroamination of 1,3-Dienes This work was supported by a Grant-in-Aid for Scientific Research from the Ministry of Education, Science, Sports and Culture, Japan.
resolves10.1021/ja056112dBismuth-Catalyzed Intermolecular Hydroamination of 1,3-Dienes with Carbamates, Sulfonamides, and Carboxamides
resolves10.1021/ja710206uCatalytic Intermolecular Linear Allylic C−H Amination via Heterobimetallic Catalysis
resolves10.1021/ja1030936Scope and Mechanism of Allylic C−H Amination of Terminal Alkenes by the Palladium/PhI(OPiv)<sub>2</sub>Catalyst System: Insights into the Effect of Naphthoquinone
resolves10.1021/ja409995wEnantioselective Functionalization of Allylic C–H Bonds Following a Strategy of Functionalization and Diversification
resolves10.1038/nchem.2366A manganese catalyst for highly reactive yet chemoselective intramolecular C(sp3)–H amination
resolves10.1021/jacs.5b11294Aerobic Linear Allylic C–H Amination: Overcoming Benzoquinone Inhibition
resolves10.1039/c1ob05238aPalladium-catalyzed mono-N-allylation of unprotected amino acids with 1,1-dimethylallyl alcohol in water
resolves10.1002/adsc.200600584Chemoselective Palladium‐Catalyzed Reaction in Aqueous Media: Selectivity in the Reaction of Haloanilines with 1,1‐Dimethylallyl Alcohol
resolves10.1021/ja0628811Synthesis of Secondary Amines by Titanium-Mediated Transfer of Alkenyl Groups from Alcohols
resolves10.1021/ol901418cGold-Catalyzed Intermolecular Markovnikov Hydroamination of Allenes with Secondary Amines
resolves10.1021/ja2020873Exercising Regiocontrol in Palladium-Catalyzed Asymmetric Prenylations and Geranylation: Unifying Strategy toward Flustramines A and B
resolves10.1021/ja507530fSelective Palladium-Catalyzed Aminocarbonylation of 1,3-Dienes: Atom-Efficient Synthesis of β,γ-Unsaturated Amides
resolves10.1021/ol202766gStereoselective Vinylation of Aryl
<i>N</i>
-(2-Pyridylsulfonyl) Aldimines with 1-Alkenyl-1,1-heterobimetallic Reagents
resolves10.1021/ja057778aCatalytic Four-Component Assembly Based on Allenylboronate Platform: New Access to Privileged Allylic Amine Structures
resolves10.1080/00397910802226564Stereoselective Synthesis of Allylic Amines by One-Pot Tandem Reaction of Acetylenic Sulfone, Grignard Reagent, and N-Tosylimine
resolves10.1002/anie.200460044Asymmetric Catalytic Coupling of Organoboranes, Alkynes, and Imines with a Removable (Trialkylsilyloxy)ethyl Group—Direct Access to Enantiomerically Pure Primary Allylic Amines
resolves10.1055/s-1995-4012A Convenient Two-Step Procedure for the Synthesis of Substituted Allylic Amines from Allylic Alcohols
resolves10.1021/ol502460jOxidative 1,4-Diamination of Dienes Using Simple Urea Derivatives
resolves10.1038/nchem.1796Ligand-enabled multiple absolute stereocontrol in metal-catalysed cycloaddition for construction of contiguous all-carbon quaternary stereocentres
resolves10.1002/anie.201403754Palladium‐Catalyzed Decarboxylative Cycloaddition of Vinylethylene Carbonates with Formaldehyde: Enantioselective Construction of Tertiary Vinylglycols
resolves10.1002/anie.201407013Palladium‐Catalyzed Asymmetric Decarboxylative Cycloaddition of Vinylethylene Carbonates with Michael Acceptors: Construction of Vicinal Quaternary Stereocenters
resolves10.1002/anie.201511521Substrate‐Controlled Product Divergence: Conversion of CO<sub>2</sub> into Heterocyclic Products
resolves10.1002/anie.201406645Carbon Dioxide as a Protecting Group: Highly Efficient and Selective Catalytic Access to Cyclic
<i>cis</i>
‐Diol Scaffolds
resolves10.1038/ncomms6500Asymmetric trapping of zwitterionic intermediates by sulphur ylides in a palladium-catalysed decarboxylation-cycloaddition sequence
resolves10.1021/ja071905g<i>syn</i>-1,2-Amino Alcohols via Diastereoselective Allylic C−H Amination
resolves10.1038/nchem.351Total synthesis and study of 6-deoxyerythronolide B by late-stage C–H oxidation
resolves10.1039/C4GC01032ARational investigations in the ring opening of cyclic carbonates by amines
resolves10.1021/ol801285gWater-Mediated Catalyst Preactivation: An Efficient Protocol for C−N Cross-Coupling Reactions
resolves10.1021/ja108074tA Multiligand Based Pd Catalyst for C−N Cross-Coupling Reactions
resolves10.1021/jo052325+Controlling Olefin Geometry with Pd Catalysis: Selective Formation of
<i>Z</i>
-olefins from Both
<i>E-</i>
and
<i>Z</i>
-Allylic Carbonates
resolves10.1021/ol0610744Decarboxylative Ring Contractions and Olefin Insertions of Vinyl Oxazinanones
resolves10.1021/ja050340qDevelopment of Aliphatic Alcohols as Nucleophiles for Palladium-Catalyzed DYKAT Reactions: Total Synthesis of (+)-Hippospongic Acid A
resolves10.1002/anie.201506083Mechanism‐Driven Elaboration of an Enantioselective Bromocyclopropanation Reaction of Allylic Alcohols
resolves10.1039/C5OB01854Danti-Selective aminofluorination of alkenes with amidines mediated by hypervalent iodine(
<scp>iii</scp>
) reagents
resolves10.1002/adsc.201300846Oxidative Heck Coupling of Allylic Amines with 2,2,6,6‐Tetramethylpiperidine‐<i>N</i>‐oxyl (TEMPO) as Oxidant for the Preparation of Tetrasubstituted Alkenes
resolves10.1002/adsc.201500876Copper(I)‐Catalyzed Synthesis of Chlorinated Tetrahydropyridazin‐3‐ones and 1,2‐Diazepan‐3‐ones from <i>N</i>‐Allyl‐<i>N</i>′‐trichloroacetylhydrazines
resolves10.1002/anie.201108211Oxidative Heck Arylation for the Stereoselective Synthesis of Tetrasubstituted Olefins Using Nitroxides as Oxidants
resolves10.1021/jacs.5b11335Enantioselective Dehydrogenative Heck Arylations of Trisubstituted Alkenes with Indoles to Construct Quaternary Stereocenters
resolves10.1038/nchem.2418A direct approach to amines with remote stereocentres by enantioselective CuH-catalysed reductive relay hydroamination
resolves10.1016/S0022-328X(00)91643-7Palladium(II)-promoted 1,4-diamination of 1,3-dienes. Stereochemistry of amination of a π-allylpalladium complex
resolves10.1021/acs.chemrev.5b00163Computational Studies of Synthetically Relevant Homogeneous Organometallic Catalysis Involving Ni, Pd, Ir, and Rh: An Overview of Commonly Employed DFT Methods and Mechanistic Insights
resolves10.1021/om800051nPalladium-Catalyzed Deallylation of Allyl Ethers with a Xanthene Phosphole Ligand. Experimental and DFT Mechanistic Studies
resolves10.1002/cssc.201200255Merging Sustainability with Organocatalysis in the Formation of Organic Carbonates by Using CO
<sub>2</sub>
as a Feedstock
resolves10.1002/chem.201103992Synthesis of PCP‐Supported Nickel Complexes and their Reactivity with Carbon Dioxide
resolves10.1002/chem.201203985A DFT Study on the Mechanism of the Cycloaddition Reaction of CO<sub>2</sub> to Epoxides Catalyzed by Zn(Salphen) Complexes
resolves10.1021/jo501837pComputational Characterization of the Mechanism for Coinage-Metal-Catalyzed Carboxylation of Terminal Alkynes
resolves10.1021/ja410541vMechanism of the Formation of Carboxylate from Alcohols and Water Catalyzed by a Bipyridine-Based Ruthenium Complex: A Computational Study
resolves10.1021/jacs.5b07444Role of the Chemically Non-Innocent Ligand in the Catalytic Formation of Hydrogen and Carbon Dioxide from Methanol and Water with the Metal as the Spectator
resolves10.1021/acscatal.5b00252Mechanistic Insight into the Gold-Catalyzed Carboxylative Cyclization of Propargylamines
resolves10.1021/om00004a039Rates and Mechanism of the Formation of Zerovalent Palladium Complexes from Mixtures of Pd(OAc)2 and Tertiary Phosphines and Their Reactivity in Oxidative Additions
resolves10.1021/om0101137Formation of Palladium(0) Complexes from Pd(OAc)<sub>2</sub> and a Bidentate Phosphine Ligand (dppp) and Their Reactivity in Oxidative Addition
resolves10.1002/anie.201210252The Impact of Palladium(II) Reduction Pathways on the Structure and Activity of Palladium(0) Catalysts
resolves10.1021/ar040063cPredicting the Stereochemistry of Diphenylphosphino Benzoic Acid (DPPBA)-Based Palladium-Catalyzed Asymmetric Allylic Alkylation Reactions: A Working Model
resolves10.1021/om020680+Effects of Bidentate Phosphine Ligands on<i>s</i><i>yn</i><i>−</i><i>anti</i>Isomerization in π-Allylpalladium Complexes
resolves10.1021/ja973150rRetention of Regiochemistry of Allylic Esters in Palladium-Catalyzed Allylic Alkylation in the Presence of a MOP Ligand
resolves10.1021/ja000547dDynamic Kinetic Asymmetric Transformation of Diene Monoepoxides: A Practical Asymmetric Synthesis of Vinylglycinol, Vigabatrin, and Ethambutol
resolves10.1021/ci500593jManaging the Computational Chemistry Big Data Problem: The
<b>ioChem-BD</b>
Platform
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