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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 of 4-Tetrazolyl-Substituted 3,4-Dihydroquinazoline Derivatives with Anticancer Activity via a One-Pot Sequential Ugi-Azide/Palladium-Catalyzed Azide-Isocyanide Cross-Coupling/Cyclization Reaction
Jun Xiong, Huiting He, He‐Yu Yang, et al.
The Journal of Organic Chemistry (2022) Vol. 87, Iss. 15, pp. 9488-9496
Closed Access | Times Cited: 21

Showing 21 citing articles:

Multicomponent Reaction-Assisted Drug Discovery: A Time- and Cost-Effective Green Approach Speeding Up Identification and Optimization of Anticancer Drugs
Giovanni Graziano, Angela Stefanachi, Marialessandra Contino, et al.
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 7, pp. 6581-6581
Open Access | Times Cited: 41
Applications of palladium-catalyzed C–N cross-coupling reactions in pharmaceutical compounds
Reza Emadi, Abbas Bahrami Nekoo, Fatemeh Molaverdi, et al.
RSC Advances (2023) Vol. 13, Iss. 27, pp. 18715-18733
Open Access | Times Cited: 27
Green and efficient one-pot three-component synthesis of novel drug-like furo[2,3-d]pyrimidines as potential active site inhibitors and putative allosteric hotspots modulators of both SARS-CoV-2 MPro and PLPro
Hossein Mousavi, Behzad Zeynizadeh, Mehdi Rimaz
Bioorganic Chemistry (2023) Vol. 135, pp. 106390-106390
Open Access | Times Cited: 26
Stereoselective Synthesis of 12-Tetrazolyl Substituted (E)-5H-Quinazolino[3,2-a]quinazolines via Sequential Ugi-Azide/Staudinger/aza-Wittig/Addition/Ag(I)-Catalyzed Cyclization
Mao-Lin Yang, Long Zhao, Hao Chen, et al.
The Journal of Organic Chemistry (2023) Vol. 88, Iss. 3, pp. 1898-1906
Closed Access | Times Cited: 14
Acid-Catalyzed, Metal- and Oxidant-Free C=C Bond Cleavage of Enaminones: One-Pot Synthesis of 3,4-Dihydroquinazolines
Ting Chen, Ting Huang, Mao-Chun Ye, et al.
Molecules (2025) Vol. 30, Iss. 2, pp. 350-350
Open Access
One-Pot Regioselective Synthesis of Spiroimidazolidinones via a Sequential Ugi 4CR/Azide-Isocyanide Coupling/Cyclization/Rearrangement/Hydroxylation Reaction
Yan‐Mei Yan, Hongbo Tong, Zhenxing Ren, et al.
Organic Letters (2025)
Closed Access
Nitrene-transfer from azides to isocyanides: Unveiling its versatility as a promising building block for the synthesis of bioactive heterocycles
Devesh M. Sawant, Gaurav Joshi, Arshad J. Ansari
iScience (2024) Vol. 27, Iss. 4, pp. 109311-109311
Open Access | Times Cited: 4
“Isocyanates and isocyanides - life-threatening toxins or essential compounds?”
Marta Pawlak, Kacper Pobłocki, Joanna Drzeżdżon, et al.
The Science of The Total Environment (2024) Vol. 934, pp. 173250-173250
Closed Access | Times Cited: 4
Synthesis of Imidazo[1,2-a]pyridine-Fused 1,3-Benzodiazepine Derivatives with Anticancer Activity via a One-Pot Cascade GBB-3CR/Pd(II)-Catalyzed Azide-Isocyanide Coupling/Cyclization Process
Cheng-Ran Zhong, Yang-Hong Zhang, Gang Yao, et al.
The Journal of Organic Chemistry (2023) Vol. 88, Iss. 18, pp. 13125-13134
Closed Access | Times Cited: 9
De novo Synthesis of Chiral 3,4‐DihydroquinazolinesviaOne‐Pot Enantioselective Ugi‐Azide/Cyclization Sequences†
Zu‐Kui Xie, Jun‐Jun Ding, Yi‐Ming Ou, et al.
Chinese Journal of Chemistry (2024) Vol. 42, Iss. 18, pp. 2140-2146
Closed Access | Times Cited: 2
2-Azidobenzaldehyde-Based [4+2] Annulation for the Synthesis of Quinoline Derivatives
Xiaofeng Zhang, Miao Liu, Weiqi Qiu, et al.
Molecules (2024) Vol. 29, Iss. 6, pp. 1241-1241
Open Access | Times Cited: 1
One-Step Construction of 1,3,4-Oxadiazoles with Anticancer Activity from Tertiary Amines via a Sequential Copper(I)-Catalyzed Oxidative Ugi/aza-Wittig Reaction
Mei Sun, Nong-Qi Mao, Sheng-Long Wang, et al.
Molecules (2024) Vol. 29, Iss. 6, pp. 1253-1253
Open Access | Times Cited: 1
Multicomponent cyclization with azides to synthesize N-heterocycles
Hong Guo, Bei Zhou, Jingjing Chang, et al.
Organic & Biomolecular Chemistry (2023) Vol. 21, Iss. 40, pp. 8054-8074
Closed Access | Times Cited: 3
2-azidobenzaldehyde: A versatile scaffold for the generation of N‐heterocyclic compounds
Fatemeh Doraghi, Somaye Karimian, Seyedeh Pegah Aledavoud, et al.
Journal of Molecular Structure (2023) Vol. 1294, pp. 136510-136510
Closed Access | Times Cited: 2
One-step Construction of 1,3,4-oxadiazoles from Tertiary Amines via a Sequential Copper(I)-Catalyzed Oxidative Ugi/aza-Wittig Reaction
Mei Sun, Nong-Qi Mao, Sheng-Long Wang, et al.
Authorea (Authorea) (2024)
Open Access
Facile synthesis of dihydroisobenzofuran derivatives via a one-pot sequential Passerini-azide/Ag(I)-catalyzed cyclization process
Yan Luo, Haifeng Yu, Yang Li-na, et al.
Tetrahedron (2024) Vol. 158, pp. 133984-133984
Closed Access
One-Pot Reductive Amination/N-Acylation/Aza-Wittig Reaction for the Synthesis of 3,4-Dihydroquinazolines
Wensheng Zhang, Wei Zheng, Guoqiang Zuo, et al.
Chinese Journal of Organic Chemistry (2024) Vol. 44, Iss. 5, pp. 1686-1686
Closed Access
Multicomponent reaction strategy to heterocyclic compounds in anticancer drug design
Suman Majee, Sakshi Priya, Vaibhav Kumar, et al.
Elsevier eBooks (2024), pp. 551-595
Closed Access
AcOH-Catalyzed Rearrangements of Benzo[e][1,4]diazepin-2(and 3)-ones: Easy Access to 1,4-Dihydroquinazolines and Their Condensed Analogues
В. А. Мамедов, Nataliya Zhukova, Victor V. Syakaev, et al.
The Journal of Organic Chemistry (2024)
Closed Access
Five-membered ring systems: with more than one N atom
Larry Yet
Progress in heterocyclic chemistry (2023), pp. 281-332
Closed Access
Six-membered ring systems: diazines and benzo derivatives
K. Alison Rinderspacher
Progress in heterocyclic chemistry (2023), pp. 427-469
Closed Access
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