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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:

Continuous Flow Enables Metallaphotoredox Catalysis in a Medicinal Chemistry Setting: Accelerated Optimization and Library Execution of a Reductive Coupling between Benzylic Chlorides and Aryl Bromides
Zachary G. Brill, Casey B. Ritts, Umar Faruk Mansoor, et al.
Organic Letters (2019) Vol. 22, Iss. 2, pp. 410-416
Closed Access | Times Cited: 39

Showing 1-25 of 39 citing articles:

Technological Innovations in Photochemistry for Organic Synthesis: Flow Chemistry, High-Throughput Experimentation, Scale-up, and Photoelectrochemistry
Laura Buglioni, Fabian Raymenants, Aidan Slattery, et al.
Chemical Reviews (2021) Vol. 122, Iss. 2, pp. 2752-2906
Open Access | Times Cited: 528
Applications of Halogen-Atom Transfer (XAT) for the Generation of Carbon Radicals in Synthetic Photochemistry and Photocatalysis
Fabio Juliá, Timothée Constantin, Daniele Leonori
Chemical Reviews (2021) Vol. 122, Iss. 2, pp. 2292-2352
Open Access | Times Cited: 373
Photocatalysis in the Life Science Industry
Lisa Candish, Karl D. Collins, Gemma C. Cook, et al.
Chemical Reviews (2021) Vol. 122, Iss. 2, pp. 2907-2980
Closed Access | Times Cited: 283
Expanding the Medicinal Chemist Toolbox: Comparing Seven C(sp2)–C(sp3) Cross-Coupling Methods by Library Synthesis
Amanda W. Dombrowski, Nathan J. Gesmundo, Ana L. Aguirre, et al.
ACS Medicinal Chemistry Letters (2020) Vol. 11, Iss. 4, pp. 597-604
Open Access | Times Cited: 157
Nickel-Catalyzed Reductive Cross-Couplings: New Opportunities for Carbon–Carbon Bond Formations through Photochemistry and Electrochemistry
Yi Liang, Tengfei Ji, Kun‐Quan Chen, et al.
CCS Chemistry (2021) Vol. 4, Iss. 1, pp. 9-30
Open Access | Times Cited: 155
Ready, Set, Flow! Automated Continuous Synthesis and Optimization
C. Breen, Anirudh M. K. Nambiar, Timothy F. Jamison, et al.
Trends in Chemistry (2021) Vol. 3, Iss. 5, pp. 373-386
Open Access | Times Cited: 102
Regioselective Cross-Electrophile Coupling of Epoxides and (Hetero)aryl Iodides via Ni/Ti/Photoredox Catalysis
Marvin Parasram, Benjamin J. Shields, Omar Ahmad, et al.
ACS Catalysis (2020) Vol. 10, Iss. 10, pp. 5821-5827
Open Access | Times Cited: 88
Rapid and Direct Photocatalytic C(sp3)−H Acylation and Arylation in Flow
Daniele Mazzarella, Antonio Pulcinella, Loïc Bovy, et al.
Angewandte Chemie International Edition (2021) Vol. 60, Iss. 39, pp. 21277-21282
Open Access | Times Cited: 74
Photoinduced Halogen-Atom Transfer by N-Heterocyclic Carbene-Ligated Boryl Radicals for C(sp3)–C(sp3) Bond Formation
Ting Wan, Luca Capaldo, Davide Ravelli, et al.
Journal of the American Chemical Society (2022) Vol. 145, Iss. 2, pp. 991-999
Open Access | Times Cited: 52
Emerging reaction technologies in pharmaceutical development: Challenges and opportunities in electrochemistry, photochemistry, and biocatalysis
Benjamin Cohen, Dan Lehnherr, Melda Sezen-Edmonds, et al.
Process Safety and Environmental Protection (2023) Vol. 192, pp. 622-637
Closed Access | Times Cited: 25
Photochemistry in Medicinal Chemistry and Chemical Biology
Wenyong Zhu, Claire Empel, Sveva Pelliccia, et al.
Journal of Medicinal Chemistry (2024) Vol. 67, Iss. 6, pp. 4322-4345
Closed Access | Times Cited: 12
Late stage C–H functionalization via chalcogen and pnictogen salts
Christopher B. Kelly, Rosaura Padilla‐Salinas
Chemical Science (2020) Vol. 11, Iss. 37, pp. 10047-10060
Open Access | Times Cited: 58
Ir/Ni Photoredox Dual Catalysis with Heterogeneous Base Enabled by an Oscillatory Plug Flow Photoreactor
Wouter Debrouwer, Wim Kimpe, Ruben Dangreau, et al.
Organic Process Research & Development (2020) Vol. 24, Iss. 10, pp. 2319-2325
Open Access | Times Cited: 54
A Widely Applicable Dual Catalytic System for Cross-Electrophile Coupling Enabled by Mechanistic Studies
David J. Charboneau, Emily L. Barth, Nilay Hazari, et al.
ACS Catalysis (2020) Vol. 10, Iss. 21, pp. 12642-12656
Open Access | Times Cited: 51
Tunable and Practical Homogeneous Organic Reductants for Cross-Electrophile Coupling
David J. Charboneau, Haotian Huang, Emily L. Barth, et al.
Journal of the American Chemical Society (2021) Vol. 143, Iss. 49, pp. 21024-21036
Open Access | Times Cited: 46
ChemBead Enabled High‐Throughput Cross‐Electrophile Coupling Reveals a New Complementary Ligand
Ana L. Aguirre, Nathan L. Loud, Keywan A. Johnson, et al.
Chemistry - A European Journal (2021) Vol. 27, Iss. 51, pp. 12981-12986
Open Access | Times Cited: 42
Nickel-Catalyzed Electroreductive Coupling of Alkylpyridinium Salts and Aryl Halides
Jiantao Fu, Windsor Lundy, Rajdip Chowdhury, et al.
ACS Catalysis (2023) Vol. 13, Iss. 14, pp. 9336-9345
Open Access | Times Cited: 18
Dual nickel- and photoredox-catalyzed carbon-carbon bond formations via reductive cross-coupling involving organohalides
Hepan Wang, Tao Xu
Chem Catalysis (2024) Vol. 4, Iss. 3, pp. 100952-100952
Closed Access | Times Cited: 5
Cross-Electrophile Coupling: Principles, Methods, and Applications in Synthesis
Lauren E. Ehehalt, Omar M. Beleh, Isabella C. Priest, et al.
Chemical Reviews (2024)
Open Access | Times Cited: 5
Cross-Electrophile Coupling to Form Sterically Hindered C(sp2)–C(sp3) Bonds: Ni and Co Afford Complementary Reactivity
Tung-Kung Wu, Anthony J. Castro, Kasturi Ganguli, et al.
Journal of the American Chemical Society (2025)
Closed Access
Enantioselective Reductive Homocoupling of Allylic Acetates Enabled by Dual Photoredox/Palladium Catalysis: Access to C2-Symmetrical 1,5-Dienes
Hong‐Hao Zhang, Menghan Tang, Jiajia Zhao, et al.
Journal of the American Chemical Society (2021) Vol. 143, Iss. 32, pp. 12836-12846
Closed Access | Times Cited: 37
Merging Halogen-Atom transfer with transition metal catalysis
Junjie Chen, Huan‐Ming Huang
Tetrahedron Letters (2022) Vol. 102, pp. 153945-153945
Closed Access | Times Cited: 19
Upscaling Photoredox Cross-Coupling Reactions in Batch Using Immersion-Well Reactors
Isabelle Grimm, Simone T. Hauer, Tim Schulte, et al.
Organic Process Research & Development (2020) Vol. 24, Iss. 6, pp. 1185-1193
Closed Access | Times Cited: 30
Predicting Performance of Photochemical Transformations for Scaling Up in Different Platforms by Combining High-Throughput Experimentation with Computational Modeling
Melda Sezen-Edmonds, José E. Tábora, Benjamin Cohen, et al.
Organic Process Research & Development (2020) Vol. 24, Iss. 10, pp. 2128-2138
Closed Access | Times Cited: 26
Tunable Redox‐Neutral Photocatalysis: Visible Light‐Induced Arylperfluoroalkylation of Alkenes Regulated by Protons
Yuan Li, Xin Zhang, Deqiang Liang, et al.
Asian Journal of Organic Chemistry (2021) Vol. 10, Iss. 3, pp. 642-648
Closed Access | Times Cited: 20
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