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References from Cyclometalated Iridium Complex-Catalyzed N -Alkylation of Amines with Alcohols via Borrowing Hydrogen in Aqueous Media. Local targets link to admitted publications; unresolved targets remain external evidence.
a- and ß-Adrenoceptors: From the Gene to the Clinic. 2. Structure-Activity Relationships and Therapeutic Applications
10.1021/jm00019a001 · 1995 · External reference
A Survey of the Borrowing Hydrogen Approach to the Synthesis of some Pharmaceutically Relevant Intermediates
10.1021/acs.oprd.5b00199 · 2015 · External reference
N-Alkylation by Hydrogen Autotransfer Reactions
10.1007/s41061-016-0034-2 · 2016 · External reference
Reductive Amination in the Synthesis of Pharmaceuticals
10.1021/acs.chemrev.9b00383 · 2019 · External reference
Advances in One-Pot Synthesis through Borrowing Hydrogen Catalysis
10.1021/acs.chemrev.7b00340 · 2018 · External reference
A bifunctional strategy for N-heterocyclic carbene-stabilized iridium complex-catalyzed N-alkylation of amines with alcohols in aqueous media
10.1039/c8gc02298d · 2019 · External reference
An Organometallic Future in Green and Energy Chemistry
10.1021/om1009439 · 2011 · External reference
Transition metal-catalyzed N-alkylation of amines by alcohols
10.1039/c39810000611 · External reference
The ruthenium catalyzed Nalkylation and N-heterocyclization of aniline using alcohols and aldehydes
10.1016/s0040-4039(01)92965-x · 1981 · External reference
Borrowing Hydrogen in the Activation of Alcohols
10.1002/adsc.200600638 · 2007 · External reference
Hydrogen Autotransfer in the N-Alkylation of Amines and Related Compounds using Alcohols and Amines as Electrophiles
10.1021/cr9002159 · 2010 · External reference
3d-Metal Catalyzed N- and C-Alkylation Reactions via Borrowing Hydrogen or Hydrogen Autotransfer
10.1021/acs.chemrev.8b00306 · 2019 · External reference
Recent advances in homogeneous borrowing hydrogen catalysis using earth-abundant first row transition metals
10.1039/c8ob01895b · 2019 · External reference
The Alkylation of Amines as Catalyzed by Nickel
10.1021/ja01340a046 · 1932 · External reference
Monoalkylation of Primary Amines and N-Sulfinylamides. Chem
10.1039/b816846f · 2009 · External reference
Heterogeneous Ni Catalysts for N-Alkylation of Amines with Alcohols
10.1021/cs4001267 · 2013 · External reference
Reinvestigating Raney Nickel Mediated Selective Alkylation of Amines with Alcohols via Hydrogen Autotransfer Methodology
10.1016/j.apcata.2014.04.009 · 2014 · External reference
Application of Design of Experiments for Optimization of Raney Nickel Mediated Borrowing Hydrogen Reaction
10.13040/ijpsr.0975-8232 · 2014 · External reference
Nickel-Catalyzed N-Alkylation of Acylhydrazines and Arylamines Using Alcohols and Enantioselective Examples
10.1002/anie.201708949 · 2017 · External reference
An Efficient and Selective Nickel-Catalyzed Direct N-Alkylation of Anilines with Alcohols
10.1021/acscatal.7b02817 · 2017 · External reference
Nickel-Catalyzed Phosphine Free Direct N-Alkylation of Amides with Alcohols
10.1021/acs.joc.7b03215 · 2018 · External reference
Solvent-Free N-Alkylation and Dehydrogenative Coupling Catalyzed by a Highly Active Pincer-Nickel Complex.
10.1021/acs.organomet.0c00233 · 2020 · External reference
Iron Catalysis in Organic Synthesis
10.1021/cr500425u · 2015 · External reference
Benzylamines via Iron- Catalyzed Direct Amination of Benzyl Alcohols
10.1021/acscatal.5b02160 · 2016 · External reference
Use of (Cyclopentadienone)Iron Tricarbonyl Complexes for C-N Bond Formation Reactions Between Amines and Alcohols
10.1021/acs.joc.7b01990 · 2017 · External reference
Iron-Catalyzed Reductive Ethylation of Imines with Ethanol
10.1002/anie.201800328 · 2018 · External reference
Iron-Catalyzed Methylation Using the Borrowing Hydrogen Approach
10.1021/acscatal.8b02158 · 2018 · External reference
Switching the N-Alkylation of Arylamines with Benzyl Alcohols to Imine Formation Enables the One-Pot Synthesis of Enantio enriched α-N-Alkylaminophosphonates
10.1002/ejoc.201900209 · 2019 · External reference
Solvent-Free N-Alkylation and Dehydrogenative Coupling Catalyzed by a Highly Active Pincer-Nickel Complex
10.1021/acs.organomet.0c00233 · 2020 · External reference
A Highly Active and Easily Accessible Cobalt Catalyst for Selective Hydrogenation of C=O Bonds
10.1021/jacs.5b04349 · 2015 · External reference
Cobalt-Catalyzed Alkylation of Aromatic Amines by Alcohols
10.1002/anie.201507955 · 2015 · External reference
Cobalt-Catalyzed N-Alkylation of Amines with Alcohols
10.1021/acs.orglett.5b03461 · 2016 · External reference
Co(II) PCP Pincer Complexes as Catalysts for the Alkylation of Aromatic Amines with Primary Alcohols
10.1021/acs.orglett.6b01647 · 2016 · External reference
Direct Access to N-Alkylated Amines and Imines via Acceptorless Dehydrogenative Coupling Catalyzed by a Cobalt(II)-NNN Pincer Complex
10.1039/c8cy00859k · 2018 · External reference
Efficient and selective N-alkylation of amines with alcohols catalysed by manganese pincer complexes
10.1038/ncomms12641 · 2016 · External reference
Improved and General Manganese-Catalyzed N-Methylation of Aromatic Amines Using Methanol
10.1002/chem.201605218 · 2017 · External reference
Mono-N-methylation of anilines with methanol catalyzed by a manganese pincer-complex
10.1016/j.jcat.2017.01.004 · 2017 · External reference
N-Substituted Hydrazones by Manganese-Catalyzed Coupling of Alcohols with Hydrazine: Borrowing Hydrogen and Acceptorless Dehydrogenation in One System
10.1002/anie.201712593 · 2018 · External reference
A Highly Active PN3 Manganese Pincer Complex Performing N-Alkylation of Amines under Mild Conditions
10.1021/acs.orglett.9b00832 · 2019 · External reference
Room temperature N-heterocyclic carbene manganese catalyzed selective N-alkylation of anilines with alcohols
10.1039/c9cc02989c · 2019 · External reference
Ag/GO nanocatalysts for N-alkylation
10.1016/j.matpr.2019.08.151 · 2020 · External reference
Tunable Triazole-Phosphine-Copper Catalysts for the Synthesis of 2-Aryl-1H-benzo[d]imidazoles from Benzyl Alcohols and Diamines by Acceptorless Dehydrogenation and Borrowing Hydrogen Reactions
10.1002/adsc.201700179 · 2017 · External reference
Alcohol Amination Catalyzed by Copper Powder as a Self-Supported Catalyst
10.1002/cssc.201801877 · 2019 · External reference
Tunable dehydrogenative amidation versus amination using a single ruthenium-NHC catalyst
10.1021/acscatal.5b00588 · 2015 · External reference
Benzimidazolium sulfonate ligand precursors and application in ruthenium-catalyzed aromatic amine alkylation with alcohols
10.1016/j.catcom.2015.10.028 · 2016 · External reference
Rutheniumcatalyzed synthesis of tri-substituted 1,3,5-triazines from alcohols and biguanides
10.1039/c6nj01620k · 2016 · External reference
Glycerol upgrading via hydrogen borrowing: Direct ruthenium-catalyzed amination of the glycerol derivative Solketal
10.1021/acssuschemeng.6b01659 · 2016 · External reference
New Iridium Catalysts for the Efficient Alkylation of Anilines by Alcohols under Mild Conditions
10.1002/chem.201001871 · 2010 · External reference
Iridium-catalysed amine alkylation with alcohols in water
10.1039/b923083a · 2010 · External reference
Use of an Iridium-Catalyzed Redox-Neutral Alcohol-Amine Coupling on Kilogram Scale for the Synthesis of a GlyT1 Inhibitor
10.1021/op200174k · 2011 · External reference
Iridium-catalysed condensation of alcohols and amines as a method for aminosugar synthesis
10.1039/c1cc12800k · 2011 · External reference
Iridium-Catalyzed Condensation of Amines and Vicinal Diols to Substituted Piperazines
10.1002/ejoc.201201099 · 2012 · External reference
Selective alkylation of amines with alcohols by Cp-star-Iridium(III) half-sandwich complexes
10.1021/ol303075h · 2013 · External reference
Alkylation of amines with alcohols and amines by a single catalyst under mild conditions
10.1002/chem.201501109 · 2015 · External reference
Highly Selective Hydroxylation and Alkoxylation of Silanes: One-Pot Silane Oxidation and Reduction of Aldehydes/Ketones
10.1021/acs.organomet.9b00716 · 2020 · External reference
Highly pH-Dependent Chemoselective Transfer Hydrogenation of α, β-Unsaturated Aldehydes in Water
10.1021/acs.organomet.9b00353 · 2019 · External reference
Borrowing Hydrogen in Water and Ionic Liquids: Iridium-Catalyzed Alkylation of Amines with Alcohols
10.1021/op100024j · 2010 · External reference
Alkylation of Amines with Alcohols and Amines by a Single Catalyst under Mild Conditions
10.1002/chem.201501109 · 2015 · External reference
Iridium-Catalyzed Condensation of Amines and Vicinal Diols to Substituted Piperazines
10.1002/ejoc.201201099 · 2012 · External reference
Mechanistic investigation of the iridium-catalysed alkylation of amines with Alcohols
10.1039/c2ob06603c · 2012 · External reference
A Highly Selective Manganese-Catalyzed Synthesis of Imines under Phosphine-Free Conditions,
10.1021/acs.organomet.9b00769 · 2020 · External reference
C-N Bond Formation Catalyzed by Ruthenium Nanoparticles Supported on N-Doped Carbon via Acceptorless Dehydrogenation to Secondary Amines, Imines, Benzimidazoles and Quinoxalines
10.1002/cctc.201801525 · 2018 · External reference
Efficient Synthesis of Amines by Iron-Catalyzed C=N TransferHydrogenation and C=O Reductive Amination
10.1002/adsc.201701316 · 2018 · External reference
Hydrogenation and Transfer Hydrogenation Promoted by Tethered Ru-S Complexes: From Cooperative Dihydrogen Activation to Hydride Abstraction/Proton Release from Dihydrogen Surrogates
10.1002/chem.201600386 · 2016 · External reference
L-Pipecolinic acid derived Lewis base organocatalyst for asymmetric reduction of N-aryl imines by trichlorosilane: effects of the side amide group on catalytic performances
10.1039/c2ob26772a · 2013 · External reference
Rhodium (III)-Catalyzed Hydroamination of Aromatic Terminal Alkynes with Anilines
10.1021/om201134j · 2012 · External reference
B(C6F5)3-catalyzed transfer hydrogenations of imines with Hantzsch esters
10.1039/c8ob00023a · 2018 · External reference
Ruthenium-catalyzed nitro and nitrile compounds coupling with alcohols: alternative route for N-substituted amine Synthesis
10.1002/chem.201003095 · 2011 · External reference
A highly efficient base-metal catalyst: chemoselective reduction of imines to amines using an abnormal-NHC-Fe (0) complex
10.1021/acs.organomet.6b00478 · 2016 · External reference
Dehydrogenation and α-functionalization of secondary amines by visible-light-mediated catalysis
10.1039/c9ob02699a · 2020 · External reference
NHC-carbene cyclopentadienyl iron based catalyst for a general and efficient hydrosilylation of imines
10.1039/c1cc14403k · 2012 · External reference
Bio-Inspired Catalytic Imine Reduction by Rhodium Complexes with Tethered Hantzsch Pyridinium Groups: Evidence for Direct Hydride Transfer from Dihydropyridine to Metal-Activated Substrate
10.1002/anie.201210086 · 2013 · External reference
Lewis acid-surfactant-combined catalyzed synthesis of 4-aminocyclopentenones from glycals. in water
10.1039/c3gc41032c · 2013 · External reference
Solvent- and catalyst-free direct reductive amination of aldehydes and ketones with Hantzsch ester: synthesis of secondary and tertiary amines
10.1016/j.tet.2013.04.046 · 2013 · External reference
Hitchhiker’s Guide to Reductive Amination
10.1055/s-0037-1611788 · 2019 · External reference
Copper (II) Triflate Catalyzed Intermolecular Aromatic Substitution of N, N-Disubstituted Anilines with Diazo Esters
10.1002/ejoc.201001083 · 2010 · External reference
[(1,3-Bis{2,6-bis(diphenylmethyl)-4-methylphenyl}imidazole-2-ylidene)PdCl2(NEt3)]: ″Throwing Away″ a Different Ancillary Ligand to Enhance the Catalytic Activity at Room Temperature
10.1002/ejic.201400072 · 2014 · External reference