OpenAlex Citation Counts

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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!

If you click the article title, you'll navigate to the article, as listed in CrossRef. If you click the Open Access links, you'll navigate to the "best Open Access location". Clicking the citation count will open this listing for that article. Lastly at the bottom of the page, you'll find basic pagination options.

Requested Article:

Poly(methylhydrosiloxane) as a green reducing agent in organophosphorus-catalysed amide bond formation
Daan F. J. Hamstra, Danny C. Lenstra, Tjeu J. Koenders, et al.
Organic & Biomolecular Chemistry (2017) Vol. 15, Iss. 30, pp. 6426-6432
Open Access | Times Cited: 31

Showing 1-25 of 31 citing articles:

Main Group Redox Catalysis of Organopnictogens: Vertical Periodic Trends and Emerging Opportunities in Group 15
Jeffrey M. Lipshultz, Gen Li, Alexander T. Radosevich
Journal of the American Chemical Society (2021) Vol. 143, Iss. 4, pp. 1699-1721
Open Access | Times Cited: 216

Amide Bond Formation Strategies: Latest Advances on a Dateless Transformation
Elisabetta Massolo, Margherita Pirola, Maurizio Benaglia
European Journal of Organic Chemistry (2020) Vol. 2020, Iss. 30, pp. 4641-4651
Open Access | Times Cited: 212

Recent developments in catalytic amide bond formation
Mihajlo Todorovic, David M. Perrin
Peptide Science (2020) Vol. 112, Iss. 6
Closed Access | Times Cited: 83

Direct Catalytic Amidations from Carboxylic Acid and Ester Derivatives: A Review
Armand Taussat, Renata Marcia de Figueiredo, Jean‐Marc Campagne
Catalysts (2023) Vol. 13, Iss. 2, pp. 366-366
Open Access | Times Cited: 32

Generation of Oxyphosphonium Ions by Photoredox/Cobaloxime Catalysis for Scalable Amide and Peptide Synthesis in Batch and Continuous‐Flow
Junqi Su, Jia‐Nan Mo, Xiangyang Chen, et al.
Angewandte Chemie International Edition (2021) Vol. 61, Iss. 5
Closed Access | Times Cited: 43

Two-Component Redox Organocatalyst for Peptide Bond Formation
Handoko Handoko, Nihar R. Panigrahi, Paramjit S. Arora
Journal of the American Chemical Society (2022) Vol. 144, Iss. 8, pp. 3637-3643
Closed Access | Times Cited: 23

Nucleophilic Substitution of Tertiary Sulfonamides: Construction of Sulfonate Esters
Xuesong Du, Gang Lu, Tao Zhang, et al.
Organic Letters (2025)
Closed Access

Sustainable organophosphorus-catalysed Staudinger reduction
Danny C. Lenstra, Peter J. Lenting, Jasmin Mecinović
Green Chemistry (2018) Vol. 20, Iss. 19, pp. 4418-4422
Closed Access | Times Cited: 32

Organophosphorus catalytic reaction based on reduction of phosphine oxide
Mengyu Pei, Anqi Tian, Qing‐Qing Yang, et al.
Green Synthesis and Catalysis (2022) Vol. 4, Iss. 2, pp. 135-149
Open Access | Times Cited: 18

A General One‐Pot Synthesis of 2H‐Indazoles Using an Organophosphorus–Silane System
Jens Schoene, Hassen Bel Abed, Peter Schmieder, et al.
Chemistry - A European Journal (2018) Vol. 24, Iss. 36, pp. 9090-9100
Closed Access | Times Cited: 30

Silicon compounds as stoichiometric coupling reagents for direct amidation
Joshua J. Davies, D. Christopher Braddock, Paul D. Lickiss
Organic & Biomolecular Chemistry (2021) Vol. 19, Iss. 31, pp. 6746-6760
Open Access | Times Cited: 22

A Strategy for Improving the Efficiency of Boronic Acid Catalysis in the Synthesis of Amides
Fatima Almetwali, Jacques Rouden, Jérôme Blanchet
European Journal of Organic Chemistry (2023) Vol. 26, Iss. 45
Closed Access | Times Cited: 8

Catalytic Staudinger Reduction at Room Temperature
Danny C. Lenstra, Joris J. Wolf, Jasmin Mecinović
The Journal of Organic Chemistry (2019) Vol. 84, Iss. 10, pp. 6536-6545
Open Access | Times Cited: 25

Structure-Based Design, Synthesis, and Biological Evaluation of the Cage–Amide Derived Orthopox Virus Replication Inhibitors
Evgenii S. Mozhaitsev, Е. В. Суслов, Daria A. Rastrepaeva, et al.
Viruses (2022) Vol. 15, Iss. 1, pp. 29-29
Open Access | Times Cited: 12

Mechanistic Insight into the Catalytic Staudinger Ligation
Paul B. White, Sjoerd J. Rijpkema, Roderick P. Bunschoten, et al.
Organic Letters (2019) Vol. 21, Iss. 4, pp. 1011-1014
Closed Access | Times Cited: 12

Synthesis of Amides from Aliphatic Acids and Amines by using of I2/TBHP at Room Temperature
S. Rambabu, Ashok Kommakula, B. Sonyanaik, et al.
ChemistrySelect (2018) Vol. 3, Iss. 4, pp. 1062-1065
Closed Access | Times Cited: 12

Choline Chloride/Urea as an Eco‐Friendly Deep Eutectic Solvent for TCT‐Mediated Amide Coupling at Room Temperature
Kimiya Salimiyan, Dariush Saberi
ChemistrySelect (2019) Vol. 4, Iss. 14, pp. 3985-3989
Closed Access | Times Cited: 11

Photoredox (NN)Mn(I) Catalysed Acceptorless Dehydrogenation: Synthesis of Amides, Aldehydes and Ketones
Abhisek Joshi, Saloni Kumari, Sabuj Kundu
Advanced Synthesis & Catalysis (2022) Vol. 364, Iss. 24, pp. 4371-4383
Closed Access | Times Cited: 7

A practical approach for oligopeptide synthesis via synergistic photoredox, cobaloxime and organophosphorus triple catalysis
Junqi Su, Jia‐Nan Mo, Guofeng Zhang, et al.
Organic Chemistry Frontiers (2023) Vol. 10, Iss. 19, pp. 4895-4904
Closed Access | Times Cited: 3

Chemoselective Synthesis of Amines from Ammonium Hydroxide and Hydroxylamine in Continuous Flow
Clément Audubert, Alexanne Bouchard, Gary Mathieu, et al.
The Journal of Organic Chemistry (2018) Vol. 83, Iss. 22, pp. 14203-14209
Closed Access | Times Cited: 9

Generation of Oxyphosphonium Ions by Photoredox/Cobaloxime Catalysis for Scalable Amide and Peptide Synthesis in Batch and Continuous‐Flow
Junqi Su, Jia‐Nan Mo, Xiangyang Chen, et al.
Angewandte Chemie (2021) Vol. 134, Iss. 5
Closed Access | Times Cited: 8

Dehydrogenative Conversions of Aldehydes and Amines to Amides Catalyzed by a Nickel(II) Pincer Complex
Peter Szwedo, Travis Jumper, Karie Sanford, et al.
Catalysts (2023) Vol. 13, Iss. 11, pp. 1423-1423
Open Access | Times Cited: 2

Preparation of 2-phospholene oxides by the isomerization of 3-phospholene oxides
Péter Bagi, Réka Herbay, Nikolett Péczka, et al.
Beilstein Journal of Organic Chemistry (2020) Vol. 16, pp. 818-832
Open Access | Times Cited: 4

N-Benzyl, N-phenethyl and N-benzyloxybenzamide derivatives inhibit amyloid-beta (Aβ42) aggregation and mitigate Aβ42-induced neurotoxicity
Yusheng Zhao, Arash Shakeri, Ahmed A. Hefny, et al.
Medicinal Chemistry Research (2024) Vol. 33, Iss. 7, pp. 1229-1241
Closed Access

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