References

Synthesis and Structure-Activity Relationships of Naftifine-Related Allylamine Antimycotics

10.1021/jm00151a019 · 1986 · External reference

Second- and Third-Generation Antihistimines in the Treatment of Urticaria

10.1046/j.1529-8019.2000.00034.x · 2000 · External reference

Zimelidine: A Review of its Pharmacological Properties and Therapeutic Efficacy in Depressive Illness

10.2165/00003495-198224030-00001 · 1982 · External reference

Unresolved reference

External reference

Strategies for the Syntheses of Pactamycin and Jogyamycin

10.1002/anie.202004560 · 2020 · External reference

Kinetic Resolution via Rh-Catalyzed C–C Activation of Cyclobutanones at Room Temperature

10.1021/jacs.9b09344 · 2019 · External reference

Nickel-Catalyzed 1,2-Diarylation of Simple Alkenyl Amides

10.1021/jacs.8b11942 · 2018 · External reference

Sequential Oxidative α-Cyanation/Anti-Markovnikov Hydroalkoxylation of Allylamines

10.1021/acs.orglett.5b02319 · 2015 · External reference

Rhodium-Catalyzed Sequential Allylic Amination and Olefin Hydroacylation Reactions: Enantioselective Synthesis of Seven-Membered Nitrogen Heterocycles

10.1002/anie.201310354 · 2014 · External reference

Tunable Catalyst-Controlled Syntheses of β- and γ-Amino Alcohols Enabled by Silver-Catalysed Nitrene Transfer

10.1038/s41929-019-0339-y · 2019 · External reference

C–H to C–N Cross-Coupling of Sulfonamides with Olefins

10.1021/jacs.7b13492 · 2018 · External reference

Enantioselective Rhodium-Catalyzed Alkenylation of Aliphatic Imines

10.1021/acs.orglett.7b02737 · 2017 · External reference

Cationic [(Iminophosphine)Nickel(Allyl)]+ Complexes as the First Example of Nickel Catalysts for Direct Hydroamination of Allenes

10.1002/chem.201605611 · 2017 · External reference

Development and Mechanistic Interrogation of Interrupted Chain-Walking in the Enantioselective Relay Heck Reaction

10.1021/jacs.0c03589 · 2020 · External reference

Intermolecular Heck Coupling with Hindered Alkenes Directed by Potassium Carboxylates

10.1002/anie.201813233 · 2019 · External reference

Nickel-Catalyzed Intermolecular Oxidative Heck Arylation Drive by Transfer Hydrogenation

10.1038/s41467-019-12949-1 · 2019 · External reference

Ni(I)-Catalyzed β,δ-Vinylarylation of γ,δ-Alkenyl α-Cyanocarboxylic Esters via Contraction of Transient Nickellacycles

10.1021/acscatal.9b03574 · 2019 · External reference

Three-Component Vicinal-Diarylation of Alkenes via Direct Transmetalation of Arylboronic Acids

10.1039/c9sc02182e · 2019 · External reference

Synthetic and Mechanistic Studies of a Versatile Heteroaryl Thioehter Directing Group for Pd(II) Catalysis

10.1021/acscatal.9b01471 · 2019 · External reference

Palladium-Catalyzed Regioselective and Stereoselective Oxidative Heck Arylation of Allylamines with Arylboronic Acids

10.1002/adsc.201300225 · 2013 · External reference

Substrate-Directable Heck Reactions with Arenediazonium Salts. The Regio- and Stereoselective Arylation of Allylamine Derivatives and Applications in the Synthesis of Naftifine and Abamines

10.1021/jo201105z · 2011 · External reference

A Highly Selective and General Palladium Catalyst for the Oxidative Heck Reaction of Electronically Nonbiased Olefins

10.1021/ja1060998 · 2010 · External reference

A General and Highly Selective Chelate-Controlled Intermolecular Oxidative Heck Reaction

10.1021/ja804120r · 2008 · External reference

A Facile Synthesis of 4-Aryl-2,3-Dihydropyrroles

10.1016/0040-4039(96)00749-6 · 1996 · External reference

Palladium-Catalyzed Cascade sp2 C–H Bond Functionalizations Allowing One-Pot Access to 4-Aryl-1,2,3,4-Tetrahydroquinolines from N-Allyl-N-Arylsulfonamides

10.1021/acscatal.6b02586 · 2016 · External reference

Palladium-Catalyzed, Chelation-Assisted Stereo- and Regioselective Synthesis of Tetrasubstituted Olefins by Oxidative Heck Arylation

10.1002/adsc.201200306 · 2012 · External reference

Construction of 3-Arylpropylamines Using Heck Arylations. The Total Synthesis of Cinacalcet Hydrochloride, Alverine, and Tolpropamine

10.1016/j.tet.2013.10.014 · 2014 · External reference

Site-Selective C(sp3)–H and C(sp2)–H Functionalization of Amines Using a Directing-Group-Guided Strategy

10.1002/adsc.202000689 · 2020 · External reference

New Strategies for the Transition-Metal Catalyzed Synthesis of Aliphatic Amines

10.1021/acs.chemrev.9b00462 · 2020 · External reference

Transient Ligand-Enabled Transition Metal-Catalyzed C–H Functionalization

10.1002/cssc.201900151 · 2019 · External reference

Combining Transition Metals and Transient Directing Groups for C–H Functionalization

10.1039/c8ra03230k · 2018 · External reference

Catalytic C(sp3)–H Bond Activation in Tertiary Alkylamines

10.1038/s41557-019-0393-8 · 2020 · External reference

Palladium-Catalyzed Enantioselective C–H Activation of Aliphatic Amines Using Chiral Anionic BINOL-Phosphoric Acid Ligands

10.1021/jacs.6b12234 · 2017 · External reference

Native Amine-Directed Site-Selective C(sp3)–H Arylation of Primary Aliphatic Amines with Aryl Iodides

10.1016/j.cclet.2019.10.034 · 2020 · External reference

One-Pot C–H Arylation/Lactamization Cascade Reaction of Free Benzylamines

10.1021/acs.joc.0c00542 · 2020 · External reference

Palladium-Catalyzed C(sp2)–H Olefination of Free Primary and Secondary 2-Phenylethylamines: Access to Tetrahydroisoquinolines

10.1021/acs.joc.9b01769 · 2019 · External reference

Native Directed Site-Selective δ-C(sp3)–H and δ-C(sp2)–H Arylation of Primary Amines

10.1021/acscatal.8b04927 · 2019 · External reference

Pd-Catalyzed γ-C(sp3)–H Fluorination of Free Amines

10.1021/jacs.9b13537 · 2020 · External reference

Transient Directing Group Enabled Pd-Catalyzed γ-C(sp3)–H Oxygenation of Alkyl Amines

10.1021/acscatal.0c01310 · 2020 · External reference

Palladium-Catalyzed C(sp3)–H Arylation of Primary Amines Using a Catalytic Alkyl Acetal to Form a Transient Directing Group

10.1002/chem.201804515 · 2018 · External reference

Site-Selective C–H Arylation of Primary Aliphatic Amines Enabled by a Catalytic Transient Directing Group

10.1038/nchem.2606 · 2017 · External reference

Carbon Dioxide-Mediated C(sp3)–H Arylation of Amine Substrates

10.1021/jacs.8b05061 · 2018 · External reference

Carbon Dioxide-Mediated C(sp2)–H Arylation of Primary and Secondary Benzylamines

10.1021/jacs.9b03375 · 2019 · External reference

Regioselective and Stereospecific Cross-Coupling of Primary Allylic Amines with Boronic Acids and Boronates Through Palladium-Catalyzed C–N Bond Cleaveage

10.1002/anie.201109171 · 2012 · External reference

Stereoselective Synthesis of cis- or trans-3,5-Disubstituted Pyrazolidines via Pd-Catalyzed Carboamination Reactions: Use of Allylic Strain to Control Product Stereochemistry Through N-Substituent Manipulation

10.1021/ja8050487 · 2008 · External reference

Cu-Catalyzed Selective Oxy-Cyanoalkylation of Allylamines with Cycloketone Oxime Esters and CO2

10.1002/cjoc.201900384 · 2020 · External reference

Oxy-Difluoroalkylation of Allylamines with CO2 via Visible-Light Photoredox Catalysis

10.1021/acs.orglett.7b03551 · 2018 · External reference

Selective Oxytrifluoromethylation of Allylamines with CO2

10.1002/anie.201603352 · 2016 · External reference

Distal Alkenyl C–H Functionalization via the Palladium/Norbornene Cooperative Catalysis

10.1021/jacs.9b11479 · 2020 · External reference

Palladium(II)-Catalyzed Stereospecific Alkenyl C–H Bond Alkylation of Allylamines with Alkyl Iodides

10.1021/acscatal.8b04415 · 2019 · External reference

Pd(II)-Catalyzed, Picolinamide-Assisted, Z-Selective γ-Arylation of Allylamines To Construct Z-Cinnamylamines

10.1021/acs.joc.7b00535 · 2017 · External reference

Construction of Cyclophane-Braced Peptide Macrocycles via Palladium-Catalyzed Picolinamide-Directed Intramolecular C(sp2)–H Arylation

10.1021/acs.orglett.0c02422 · 2020 · External reference

Regioselective Palladium-Catalyzed Synthesis of β-Arylated Primary Allylamine Equivalents by an Efficient Pd–N Coordination

10.1021/jo001416y · 2001 · External reference

Achieving Moderate Pressures in Sealed Vessels Using Dry Ice As a Solid CO2 Source

10.3791/58281 · 2018 · External reference

An Organic Cation as a Silver(I) Analogue for the Arylation of sp2 and sp3 C–G Bonds with Iodoarenes

10.1039/c4sc01215a · 2014 · External reference

Carbon Dioxide-Catalyzed Stereoselective Cyanation Reaction

10.1021/acscatal.9b01087 · 2019 · External reference

Carbon Dioxide as a Reversible Amine-Protecting Agent in Selective Michael Additions and Acylations

10.1039/c3gc40568k · 2013 · External reference

Supercritical Carbon Dioxide as Solvent and Temporary Protecting Group for Rhodium-Catalyzed Hydroaminomethylation

10.1002/1521-3765(20011105)7:21<4584::aid-chem4584>3.0.co;2-p · 2001 · External reference

Olefin Metathesis in Supercritical Carbon Dioxide

10.1021/ja010952k · 2001 · External reference

Kinetics of the Reaction Between Carbon-Dioxide and Tertiary Amines

10.1021/jo00291a056 · 1990 · External reference

Overcoming the Limitations of Directed C–H Functionalizations of Heterocycles

10.1038/nature13885 · 2014 · External reference

The Development and Mechanistic Investigation of a Palladium-Catalyzed 1,3-arylfluorination of Chromones

10.1039/c6sc05102b · 2017 · External reference

Understanding the Insertion Pathways and Chain Walking Mechanisms of α-Diimine Nickel Catalysts for α-Olefin Polymerization: A 13C NMR Spectroscopic Investigation

10.1021/acs.macromol.7b01150 · 2017 · External reference

Palladium-Catalyzed Oxidation of β-C(sp3)–H Bonds of Primary Alkylamines through a Rare Four-Membered Palladacycle Intermediate

10.1021/jacs.0c01629 · 2020 · External reference

A Class of N–O-Type Oxidants To Access High-Valent Palladium Species

10.1021/acs.organomet.8b00712 · 2019 · External reference

The α-Tertiary Amine Motif Drives Remarkable Selectivity for Pd-Catalyzed Carbonylation of β-Methylene C–H Bonds

10.1039/c7sc03876c · 2017 · External reference

Resolving Heterogeneity Problems and Impurity Artifacts in Operationally Homogeneous Transition Metal Catalysts

10.1021/cr2002905 · 2012 · External reference

On the Nature of the Active Species in Palladium Catalyzed Mizoroki–Heck and Suzuki–Miyaura Couplings – Homogeneous or Heterogeneous Catalysis, a Critical Review

10.1002/adsc.200505473 · 2006 · External reference

Alkenylpyridine and Alkenylamine Complexes of Palladium

10.1023/a:1007188628135 · 2001 · External reference

When Applying the Mercury Poisoning Test to Palladacycle-Catalyzed Reactions, One Should Not Consider the Common Misconception of Mercury(0) Selectivity

10.1021/acs.organomet.8b00363 · 2018 · External reference

Palladium Nanoparticles Supported on UiO-66-NH2 as Heterogeneous Catalyst for Epoxidation of Styrene

10.1016/j.inoche.2018.12.010 · 2019 · External reference

On the Interpretation of Deuterium Kinetic Isotope Effects in C–H Bond Functionalizations by Transition-Metal Complexes

10.1002/anie.201107334 · 2012 · External reference

Enhancement of CO2 Absorption in Water Through pH Control and Carbonic Anhydrase–A Technical Assessment

10.1021/acs.iecr.9b02688 · 2019 · External reference

CO2 Capture With Absorbents of Tertiary Amine Functionalized Nano–SiO2

10.3389/fchem.2020.00146 · 2020 · External reference

Palladium-Catalysed C–H Activation of Aliphatic Amines to Give Strained Nitrogen Heterocycles

10.1038/nature13389 · 2014 · External reference

Is Silver a Mere Terminal Oxidant in Palladium Catalyzed C–H Bond Activation Reactions?

10.1039/c9sc04540f · 2020 · External reference