Research graph
References from Visible-Light-Mediated C–N Cross-Coupling through Direct Sensitization of the Ni–BINAM Complex. Local targets link to admitted publications; unresolved targets remain external evidence.
Analysis of the Structural Diversity, Substitution Patterns, and Frequency of Nitrogen Heterocycles among U.S. FDA Approved Pharmaceuticals
10.1021/jm501100b · 2014 · External reference
A Review on Recent Advances in Nitrogen-Containing Molecules and Their Biological Applications
10.3390/molecules25081909 · 2020 · External reference
Applications of Palladium-Catalyzed C–N Cross-Coupling Reactions
10.1021/acs.chemrev.6b00512 · 2016 · External reference
Applications of palladium-catalyzed C–N cross-coupling reactions in pharmaceutical compounds
10.1039/d2ra07412e · 2023 · External reference
Total synthesis of (+)-Dixiamycin C via a late-stage Ni(II)-photoredox N-arylation of carbazoles
10.1021/acs.orglett.4c02436 · 2024 · External reference
Total synthesis and antiviral activity of indolosesquiterpenoids from the xiamycin and oridamycin families
10.1038/ncomms7096 · 2015 · External reference
Ueber eine neue Bildungsweise von Diphenylaminderivaten
10.1002/cber.190303602174 · 1903 · External reference
Ueber Phenylirungen bei Gegenwart von Kupfer als Katalysator
10.1002/cber.19060390298 · 1906 · External reference
A Simple Catalytic Method for the Conversion of Aryl Bromides to Arylamines
10.1002/anie.199513481 · 1995 · External reference
Palladium-catalyzed synthesis of arylamines from aryl halides. Mechanistic studies lead to coupling in the absence of tin reagents
10.1016/0040-4039(95)00605-c · 1995 · External reference
Palladium-Catalyzed Reaction of Stannylamines with Aryl Bromides. Preparation of N,N-Diethylanilines
10.1246/cl.1983.927 · 1983 · External reference
Palladium-Catalyzed Amination of Aryl Iodides Utilizing General and Efficient Procedures in the Presence of Tin-Free Benzophenone Imine
10.1021/ja964391m · 1997 · External reference
Ni-Catalyzed Amination Reactions: An Overview
10.1002/tcr.201500305 · 2016 · External reference
The Buchwald–Hartwig Amination After 25 Years
10.1002/anie.201904795 · 2019 · External reference
Recent Advances and Perspectives in the Copper-Catalysed Amination of Aryl and Heteroaryl Halides
10.1002/slct.201904436 · 2020 · External reference
Aryl amination using ligand-free Ni(II) salts and photoredox catalysis
10.1126/science.aag0209 · 2016 · External reference
Highly Chemoselective Iridium Photoredox and Nickel Catalysis for the Cross-Coupling of Primary Aryl Amines with Aryl Halides
10.1002/anie.201604429 · 2016 · External reference
Nickel Dual Photoredox Catalysis for the Synthesis of Aryl Amines
10.1021/acs.organomet.8b00121 · 2018 · External reference
Exploring visible light for carbon–nitrogen and carbon–oxygen bond formation via nickel catalysis
10.1039/d2qo01700h · 2023 · External reference
Nickel Metallaphotoredox Buchwald–Hartwig Amination Reactions: A Perspective on Irradiation Light Wavelength
10.1002/ejoc.202300933 · 2024 · External reference
Strongly Reducing, Visible-Light Organic Photoredox Catalysts as Sustainable Alternatives to Precious Metals
10.1002/chem.201702926 · 2017 · External reference
Visible-light-initiated nickel-catalyzed amination of aryl halides using thioxanthen-9-one as a photocatalyst
10.1039/d3qo00545c · 2023 · External reference
The Nickel Age in Synthetic Dual Photocatalysis: A Bright Trip Toward Materials Science
10.1002/cssc.202201094 · 2022 · External reference
General cross-coupling reactions with adaptive dynamic homogeneous catalysis
10.1038/s41586-023-06087-4 · 2023 · External reference
Energy Transfer to Ni-Amine Complexes in Dual Catalytic, Light-Driven C–N Cross-Coupling Reactions
10.1021/jacs.9b11049 · 2019 · External reference
Intraligand Charge Transfer Enables Visible-Light-Mediated Nickel-Catalyzed Cross-Coupling Reactions
10.1002/anie.202211433 · 2022 · External reference
Chiral Arylated Amines via C–N Coupling of Chiral Amines with Aryl Bromides Promoted by Light
10.1002/anie.202108587 · 2021 · External reference
General Method for the Amination of Aryl Halides with Primary and Secondary Alkyl Amines via Nickel Photocatalysis
10.1021/acs.joc.2c01284 · 2022 · External reference
Photoinduced Nickel-Catalyzed Carbon–Heteroatom Coupling
10.1002/chem.202202385 · 2023 · External reference
Recent Advance in Single Nickel Photocatalysis for Carbon-Heteroatom Bond Formation
10.1002/cctc.202300303 · 2023 · External reference
Photochemical Synthesis of Anilines via Ni-Catalyzed Coupling of Aryl Halides with Ammonium Salts
10.1021/acscatal.2c04959 · 2022 · External reference
d-Glucosamine as an efficient ligand for the copper-catalyzed selective synthesis of anilines from aryl halides and NaN3
10.1039/c1gc15469a · 2011 · External reference
d-Glucosamine as a green ligand for copper catalyzed synthesis of primary aryl amines from aryl halides and ammonia
10.1039/c1cc10568j · 2011 · External reference
C–N Cross-Coupling via Photoexcitation of Nickel–Amine Complexes
10.1021/jacs.8b03744 · 2018 · External reference
Energy Transfer to Ni-Amine Complexes in Dual Catalytic, Light-Driven C–N Cross-Coupling Reactions
10.1021/jacs.9b11049 · 2019 · External reference
A Simple Catalytic Method for the Conversion of Aryl Bromides to Arylamines
10.1002/anie.199513481 · ExternalCitation · doi-reference
Highly Chemoselective Iridium Photoredox and Nickel Catalysis for the Cross-Coupling of Primary Aryl Amines with Aryl Halides
10.1002/anie.201604429 · ExternalCitation · doi-reference
The Buchwald–Hartwig Amination After 25 Years
10.1002/anie.201904795 · ExternalCitation · doi-reference
Chiral Arylated Amines via C–N Coupling of Chiral Amines with Aryl Bromides Promoted by Light
10.1002/anie.202108587 · ExternalCitation · doi-reference
Intraligand Charge Transfer Enables Visible-Light-Mediated Nickel-Catalyzed Cross-Coupling Reactions
10.1002/anie.202211433 · ExternalCitation · doi-reference
Ueber eine neue Bildungsweise von Diphenylaminderivaten
10.1002/cber.190303602174 · ExternalCitation · doi-reference
Ueber Phenylirungen bei Gegenwart von Kupfer als Katalysator
10.1002/cber.19060390298 · ExternalCitation · doi-reference
Recent Advance in Single Nickel Photocatalysis for Carbon-Heteroatom Bond Formation
10.1002/cctc.202300303 · ExternalCitation · doi-reference
Strongly Reducing, Visible-Light Organic Photoredox Catalysts as Sustainable Alternatives to Precious Metals
10.1002/chem.201702926 · ExternalCitation · doi-reference
Photoinduced Nickel-Catalyzed Carbon–Heteroatom Coupling
10.1002/chem.202202385 · ExternalCitation · doi-reference
The Nickel Age in Synthetic Dual Photocatalysis: A Bright Trip Toward Materials Science
10.1002/cssc.202201094 · ExternalCitation · doi-reference
Nickel Metallaphotoredox Buchwald–Hartwig Amination Reactions: A Perspective on Irradiation Light Wavelength
10.1002/ejoc.202300933 · ExternalCitation · doi-reference
Recent Advances and Perspectives in the Copper-Catalysed Amination of Aryl and Heteroaryl Halides
10.1002/slct.201904436 · ExternalCitation · doi-reference
Ni-Catalyzed Amination Reactions: An Overview
10.1002/tcr.201500305 · ExternalCitation · doi-reference
Palladium-catalyzed synthesis of arylamines from aryl halides. Mechanistic studies lead to coupling in the absence of tin reagents
10.1016/0040-4039(95)00605-c · ExternalCitation · doi-reference
Applications of Palladium-Catalyzed C–N Cross-Coupling Reactions
10.1021/acs.chemrev.6b00512 · ExternalCitation · doi-reference
General Method for the Amination of Aryl Halides with Primary and Secondary Alkyl Amines via Nickel Photocatalysis
10.1021/acs.joc.2c01284 · ExternalCitation · doi-reference
Nickel Dual Photoredox Catalysis for the Synthesis of Aryl Amines
10.1021/acs.organomet.8b00121 · ExternalCitation · doi-reference
Total synthesis of (+)-Dixiamycin C via a late-stage Ni(II)-photoredox N-arylation of carbazoles
10.1021/acs.orglett.4c02436 · ExternalCitation · doi-reference
Photochemical Synthesis of Anilines via Ni-Catalyzed Coupling of Aryl Halides with Ammonium Salts
10.1021/acscatal.2c04959 · ExternalCitation · doi-reference
Palladium-Catalyzed Amination of Aryl Iodides Utilizing General and Efficient Procedures in the Presence of Tin-Free Benzophenone Imine
10.1021/ja964391m · ExternalCitation · doi-reference
C–N Cross-Coupling via Photoexcitation of Nickel–Amine Complexes
10.1021/jacs.8b03744 · ExternalCitation · doi-reference
Energy Transfer to Ni-Amine Complexes in Dual Catalytic, Light-Driven C–N Cross-Coupling Reactions
10.1021/jacs.9b11049 · ExternalCitation · doi-reference
Analysis of the Structural Diversity, Substitution Patterns, and Frequency of Nitrogen Heterocycles among U.S. FDA Approved Pharmaceuticals
10.1021/jm501100b · ExternalCitation · doi-reference
Total synthesis and antiviral activity of indolosesquiterpenoids from the xiamycin and oridamycin families
10.1038/ncomms7096 · ExternalCitation · doi-reference
General cross-coupling reactions with adaptive dynamic homogeneous catalysis
10.1038/s41586-023-06087-4 · ExternalCitation · doi-reference
d-Glucosamine as a green ligand for copper catalyzed synthesis of primary aryl amines from aryl halides and ammonia
10.1039/c1cc10568j · ExternalCitation · doi-reference
d-Glucosamine as an efficient ligand for the copper-catalyzed selective synthesis of anilines from aryl halides and NaN3
10.1039/c1gc15469a · ExternalCitation · doi-reference
Exploring visible light for carbon–nitrogen and carbon–oxygen bond formation via nickel catalysis
10.1039/d2qo01700h · ExternalCitation · doi-reference
Applications of palladium-catalyzed C–N cross-coupling reactions in pharmaceutical compounds
10.1039/d2ra07412e · ExternalCitation · doi-reference
Visible-light-initiated nickel-catalyzed amination of aryl halides using thioxanthen-9-one as a photocatalyst
10.1039/d3qo00545c · ExternalCitation · doi-reference
Aryl amination using ligand-free Ni(II) salts and photoredox catalysis
10.1126/science.aag0209 · ExternalCitation · doi-reference
Palladium-Catalyzed Reaction of Stannylamines with Aryl Bromides. Preparation of N,N-Diethylanilines
10.1246/cl.1983.927 · ExternalCitation · doi-reference
A Review on Recent Advances in Nitrogen-Containing Molecules and Their Biological Applications
10.3390/molecules25081909 · ExternalCitation · doi-reference
