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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:

Synthesis and Biological Evaluation of Quinaldopeptin
Katsushi Katayama, Takuya Okamura, Takuya Sunadome, et al.
The Journal of Organic Chemistry (2014) Vol. 79, Iss. 6, pp. 2580-2590
Closed Access | Times Cited: 17

Showing 17 citing articles:

Cutting-Edge and Time-Honored Strategies for Stereoselective Construction of C–N Bonds in Total Synthesis
Artur K. Mailyan, John A. Eickhoff, Anastasiia S. Minakova, et al.
Chemical Reviews (2016) Vol. 116, Iss. 7, pp. 4441-4557
Closed Access | Times Cited: 154
The Ugi three-component reaction and its variants
Julio C. Flores-Reyes, Alejandro Islas‐Jácome, Eduardo González‐Zamora
Organic Chemistry Frontiers (2021) Vol. 8, Iss. 19, pp. 5460-5515
Closed Access | Times Cited: 70
Cyclic Imines in Ugi and Ugi-Type Reactions
Mohammad Taghi Nazeri, Hassan Farhid, Reza Mohammadian, et al.
ACS Combinatorial Science (2020) Vol. 22, Iss. 8, pp. 361-400
Closed Access | Times Cited: 60
Diastereoselectivity in Passerini Reactions of Chiral Aldehydes and in Ugi Reactions of Chiral Cyclic Imines
Chiara Lambruschini, Lisa Moni, Luca Banfi
European Journal of Organic Chemistry (2020) Vol. 2020, Iss. 25, pp. 3766-3778
Closed Access | Times Cited: 24
Advances of Ugi reaction in natural product synthesis
Wen Zhang, Pei Tang, Mohamed Aamer Abubaker, et al.
Green Synthesis and Catalysis (2024)
Open Access | Times Cited: 2
Natural Product Bis-Intercalator Depsipeptides as a New Class of Payloads for Antibody–Drug Conjugates
Anokha S. Ratnayake, Liping Chang, L. Nathan Tumey, et al.
Bioconjugate Chemistry (2018) Vol. 30, Iss. 1, pp. 200-209
Closed Access | Times Cited: 17
The fully‐extended conformation in peptides and proteins
Marco Crisma, Fernando Formaggio, Carlos Alemán, et al.
Peptide Science (2018) Vol. 110, Iss. 5
Open Access | Times Cited: 14
Efficient Diastereoselective Three‐Component Synthesis of Pipecolic Amides
Gydo van der Heijden, Timo B. van Schaik, Valentinos Mouarrawis, et al.
European Journal of Organic Chemistry (2019) Vol. 2019, Iss. 31-32, pp. 5313-5325
Open Access | Times Cited: 12
Stereoselective synthesis of functionalized 1,2,3,4-tetrahydroisoquinolines (THIQs) via highly diastereoselective Ugi three-component reactions (U3CRs) with chiral 3,4-dihydroisoquinolines (DHIQs)
Triparagiri Ramanivas, G. Gayatri, D. Priyanka, et al.
RSC Advances (2015) Vol. 5, Iss. 90, pp. 73373-73380
Closed Access | Times Cited: 11
Design, Synthesis, and Conformation–Activity Study of Unnatural Bridged Bicyclic Depsipeptides as Highly Potent Hypoxia Inducible Factor-1 Inhibitors and Antitumor Agents
Kota Koike, Masanobu Nagano, Masahiro Ebihara, et al.
Journal of Medicinal Chemistry (2020) Vol. 63, Iss. 8, pp. 4022-4046
Closed Access | Times Cited: 11
Stereodivergent access to all four stereoisomers of chiral tetrahydrobenzo[f][1,4]oxazepines, through highly diastereoselective multicomponent Ugi–Joullié reaction
Alessandro Pinna, Andrea Basso, Chiara Lambruschini, et al.
RSC Advances (2020) Vol. 10, Iss. 2, pp. 965-972
Open Access | Times Cited: 9
Structure–Activity Relationships of Bis-Intercalating Peptides and Their Application as Antibody–Drug Conjugate Payloads
Mark E. Petersen, Michael G. Brant, Manuel Lasalle, et al.
Journal of Medicinal Chemistry (2023) Vol. 66, Iss. 12, pp. 8288-8309
Closed Access | Times Cited: 3
Antineoplastic Agents. 605. Isoquinstatins
George R. Pettit, Noeleen Melody, Jean‐Charles Chapuis
Journal of Natural Products (2017) Vol. 81, Iss. 3, pp. 451-457
Closed Access | Times Cited: 8
Total synthesis of pseudouridimycin and its epimer via Ugi-type multicomponent reaction
Ryotaro Okawa, Courtney C. Aldrich, Satoshi Ichikawa
Chemical Communications (2022) Vol. 58, Iss. 57, pp. 7956-7959
Closed Access | Times Cited: 4
Synthesis and biological evaluation of echinomycin analogues as potential colon cancer agent
Keita Kojima, Hiroaki Konishi, Kyoka Momosaki, et al.
Scientific Reports (2024) Vol. 14, Iss. 1
Open Access
Natural Product Synthesis by Multicomponent Reaction and Structure-activity Relationship Study
Takuya Chiba, Takeshi Nakaya, Katsushi Katayama, et al.
Journal of Synthetic Organic Chemistry Japan (2016) Vol. 74, Iss. 5, pp. 426-440
Closed Access | Times Cited: 2
ChemInform Abstract: Synthesis and Biological Evaluation of Quinaldopeptin.
Katsushi Katayama, Takuya Okamura, Takuya Sunadome, et al.
ChemInform (2014) Vol. 45, Iss. 35
Closed Access
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