OpenAlex is a bibliographic catalogue of scientific papers, authors and institutions accessible in open access mode, named after the Library of Alexandria. It's citation coverage is excellent and I hope you will find utility in this listing of citing articles!
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Requested Article:
Selective Buchwald–Hartwig arylation ofC-amino-1,2,4-triazoles and other coordinating aminoheterocycles enabled by bulky NHC ligands and TPEDO activator
Alexander V. Astakhov, Andrey Yu. Chernenko, Vadim V. Kutyrev, et al.
Inorganic Chemistry Frontiers (2022) Vol. 10, Iss. 1, pp. 218-239
Closed Access | Times Cited: 8
Alexander V. Astakhov, Andrey Yu. Chernenko, Vadim V. Kutyrev, et al.
Inorganic Chemistry Frontiers (2022) Vol. 10, Iss. 1, pp. 218-239
Closed Access | Times Cited: 8
Showing 8 citing articles:
Base‐Ionizable Anionic NHC Ligands in Pd‐catalyzed Reactions of Aryl Chlorides
Andrey Yu. Chernenko, V. A. Baydikova, Vadim V. Kutyrev, et al.
ChemCatChem (2023) Vol. 16, Iss. 5
Closed Access | Times Cited: 6
Andrey Yu. Chernenko, V. A. Baydikova, Vadim V. Kutyrev, et al.
ChemCatChem (2023) Vol. 16, Iss. 5
Closed Access | Times Cited: 6
Synthesis of 5-(Aryl)amino-1,2,3-triazole-containing 2,1,3-Benzothiadiazoles via Azide–Nitrile Cycloaddition Followed by Buchwald–Hartwig Reaction
Pavel S. Gribanov, Anna N. Philippova, Maxim A. Topchiy, et al.
Molecules (2024) Vol. 29, Iss. 9, pp. 2151-2151
Open Access | Times Cited: 1
Pavel S. Gribanov, Anna N. Philippova, Maxim A. Topchiy, et al.
Molecules (2024) Vol. 29, Iss. 9, pp. 2151-2151
Open Access | Times Cited: 1
A Simple Protocol for the C−N Cross‐Coupling of Aryl Chlorides with Amines Applying Ni/NHC Catalysis
Oleg V. Khazipov, Anastasia S. Pyatachenko, Victor M. Chernyshev, et al.
ChemCatChem (2023) Vol. 15, Iss. 13
Closed Access | Times Cited: 3
Oleg V. Khazipov, Anastasia S. Pyatachenko, Victor M. Chernyshev, et al.
ChemCatChem (2023) Vol. 15, Iss. 13
Closed Access | Times Cited: 3
Heteroleptic Anionic Cobalt(II) Pivalate Complex with a Bridging Trimethylsiloxy Ligand: Synthesis, Structure, and Formation Mechanism
Pavel A. Petrov, Stanislav A. Nikolaevskii, Dmitriy S. Yambulatov, et al.
Russian Journal of Inorganic Chemistry (2023) Vol. 68, Iss. 9, pp. 1228-1236
Closed Access | Times Cited: 3
Pavel A. Petrov, Stanislav A. Nikolaevskii, Dmitriy S. Yambulatov, et al.
Russian Journal of Inorganic Chemistry (2023) Vol. 68, Iss. 9, pp. 1228-1236
Closed Access | Times Cited: 3
C(5)—H arylation of 1-substituted 1,2,4-triazoles with aryl halides under Pd/NHC catalysis
Alexander V. Astakhov, Andrey Yu. Chernenko, Vadim V. Kutyrev, et al.
Russian Chemical Bulletin (2024) Vol. 73, Iss. 4, pp. 950-956
Closed Access
Alexander V. Astakhov, Andrey Yu. Chernenko, Vadim V. Kutyrev, et al.
Russian Chemical Bulletin (2024) Vol. 73, Iss. 4, pp. 950-956
Closed Access
Structural and catalytic studies of Six-Membered amino N-Heterocyclic carbene palladium (II) complexes with a triazine backbone for Suzuki coupling reaction
Ming‐Tsz Chen, Cheng‐Chun Huang, Ching‐Wei Chang, et al.
Inorganica Chimica Acta (2024), pp. 122466-122466
Closed Access
Ming‐Tsz Chen, Cheng‐Chun Huang, Ching‐Wei Chang, et al.
Inorganica Chimica Acta (2024), pp. 122466-122466
Closed Access
Fe3O4@TiO2 nanoparticles catalyzed and NaBH4 assisted one-pot reductive amination of aldehydes at ambient condition
Sajid Pinjari, Gopinath Shirole, Bhagwat K. Uphade, et al.
Research on Chemical Intermediates (2023) Vol. 49, Iss. 11, pp. 4973-4996
Closed Access | Times Cited: 1
Sajid Pinjari, Gopinath Shirole, Bhagwat K. Uphade, et al.
Research on Chemical Intermediates (2023) Vol. 49, Iss. 11, pp. 4973-4996
Closed Access | Times Cited: 1
Разнолигандный анионный комплекс пивалата кобальта(II) с мостиковым триметилсилоксолигандом: синтез, строение и механизм формирования
Pavel A. Petrov, Stanislav A. Nikolaevskii, Д. С. Ямбулатов, et al.
Журнал неорганической химии (2023) Vol. 68, Iss. 9, pp. 1255-1264
Closed Access
Pavel A. Petrov, Stanislav A. Nikolaevskii, Д. С. Ямбулатов, et al.
Журнал неорганической химии (2023) Vol. 68, Iss. 9, pp. 1255-1264
Closed Access
