
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:
A New Family of Fused Azolo[1,5-a]pteridines and Azolo[5,1-b]purines
Denis A. Gazizov, Evgeny B. Gorbunov, Gennady L. Rusinov, et al.
ACS Omega (2020) Vol. 5, Iss. 29, pp. 18226-18233
Open Access | Times Cited: 16
Denis A. Gazizov, Evgeny B. Gorbunov, Gennady L. Rusinov, et al.
ACS Omega (2020) Vol. 5, Iss. 29, pp. 18226-18233
Open Access | Times Cited: 16
Showing 16 citing articles:
Functional Pyrazolo[1,5-a]pyrimidines: Current Approaches in Synthetic Transformations and Uses As an Antitumor Scaffold
Andres Arias-Gómez, A. Godoy, Jaime Portilla
Molecules (2021) Vol. 26, Iss. 9, pp. 2708-2708
Open Access | Times Cited: 84
Andres Arias-Gómez, A. Godoy, Jaime Portilla
Molecules (2021) Vol. 26, Iss. 9, pp. 2708-2708
Open Access | Times Cited: 84
From N atom to C–NO2 group: Achieving a high energy density material with a “NH2–NO2–NH2” block
Zhiwei Zeng, Yuji Liu, Qianyang Lv, et al.
Chemical Engineering Journal (2022) Vol. 450, pp. 138094-138094
Closed Access | Times Cited: 22
Zhiwei Zeng, Yuji Liu, Qianyang Lv, et al.
Chemical Engineering Journal (2022) Vol. 450, pp. 138094-138094
Closed Access | Times Cited: 22
Nitration of Pyrrolo[2,1-a]isoquinolines
Xiao‐Hui Chen, Dandan Ma, Xin Gao, et al.
The Journal of Organic Chemistry (2023) Vol. 88, Iss. 7, pp. 4649-4661
Closed Access | Times Cited: 12
Xiao‐Hui Chen, Dandan Ma, Xin Gao, et al.
The Journal of Organic Chemistry (2023) Vol. 88, Iss. 7, pp. 4649-4661
Closed Access | Times Cited: 12
Pyrazolo[1,5-a]pyrimidine with similar “amino–nitro–amino” arrangement characteristics to TATB: a novel heat-resistant explosive with fused structure
Feng Yang, Yuangang Xu, Pengcheng Wang, et al.
CrystEngComm (2021) Vol. 23, Iss. 15, pp. 2801-2808
Closed Access | Times Cited: 21
Feng Yang, Yuangang Xu, Pengcheng Wang, et al.
CrystEngComm (2021) Vol. 23, Iss. 15, pp. 2801-2808
Closed Access | Times Cited: 21
Different Synthetic Methods for the Preparation of Triazolopyrimidines and their Biological Profile
Achraf Hibot, Asmaa Oumessaoud, Abderrafia Hafid, et al.
ChemistrySelect (2023) Vol. 8, Iss. 23
Open Access | Times Cited: 8
Achraf Hibot, Asmaa Oumessaoud, Abderrafia Hafid, et al.
ChemistrySelect (2023) Vol. 8, Iss. 23
Open Access | Times Cited: 8
Obtaining superior high-density fused-ring energetic materials via the introduction of carbonyl, o-NH2–NO2 and nitroamino groups
Xiaoyu Guo, Yizhen Feng, Shengjie Zhi, et al.
Dalton Transactions (2024) Vol. 53, Iss. 9, pp. 4035-4040
Closed Access | Times Cited: 2
Xiaoyu Guo, Yizhen Feng, Shengjie Zhi, et al.
Dalton Transactions (2024) Vol. 53, Iss. 9, pp. 4035-4040
Closed Access | Times Cited: 2
Nitration of Pyrrolo[2,1‐a]isoquinolines with NaNO2/HFIP
Xiang Huang, Yun‐Meng Li, Jing Zhou, et al.
European Journal of Organic Chemistry (2024) Vol. 27, Iss. 16
Closed Access | Times Cited: 2
Xiang Huang, Yun‐Meng Li, Jing Zhou, et al.
European Journal of Organic Chemistry (2024) Vol. 27, Iss. 16
Closed Access | Times Cited: 2
Access to azolopyrimidine-6,7-diamines as a valuable “building-blocks” to develop new fused heteroaromatic systems
Denis A. Gazizov, Victor V. Fedotov, Konstantin A. Chistyakov, et al.
Tetrahedron (2021) Vol. 89, pp. 132172-132172
Closed Access | Times Cited: 9
Denis A. Gazizov, Victor V. Fedotov, Konstantin A. Chistyakov, et al.
Tetrahedron (2021) Vol. 89, pp. 132172-132172
Closed Access | Times Cited: 9
Oxidative Aromatization of 4,7-Dihydro-6-nitroazolo[1,5-a]pyrimidines: Synthetic Possibilities and Limitations, Mechanism of Destruction, and the Theoretical and Experimental Substantiation
Daniil N. Lyapustin, Evgeny N. Ulomsky, I. A. Balyakin, et al.
Molecules (2021) Vol. 26, Iss. 16, pp. 4719-4719
Open Access | Times Cited: 9
Daniil N. Lyapustin, Evgeny N. Ulomsky, I. A. Balyakin, et al.
Molecules (2021) Vol. 26, Iss. 16, pp. 4719-4719
Open Access | Times Cited: 9
A facile approach to [1,2,4]triazolo[3,4‐i]purine via PIDA oxidation ring‐closing reaction
Xiangbin Sun, Mingwu Yu, Xianfeng Mu, et al.
Journal of Heterocyclic Chemistry (2021) Vol. 58, Iss. 12, pp. 2270-2279
Closed Access | Times Cited: 8
Xiangbin Sun, Mingwu Yu, Xianfeng Mu, et al.
Journal of Heterocyclic Chemistry (2021) Vol. 58, Iss. 12, pp. 2270-2279
Closed Access | Times Cited: 8
Novel polynitro azoxypyrazole-based energetic materials with high performance
Pengju Yang, Hongwei Yang, Ying Zhao, et al.
Dalton Transactions (2021) Vol. 50, Iss. 45, pp. 16499-16503
Closed Access | Times Cited: 8
Pengju Yang, Hongwei Yang, Ying Zhao, et al.
Dalton Transactions (2021) Vol. 50, Iss. 45, pp. 16499-16503
Closed Access | Times Cited: 8
A novel [1,2,4]triazolo[1,5-a]pteridine framework: Synthesis, photophysical properties and material studies
Denis A. Gazizov, Alexander S. Steparuk, Nadezhda S. Demina, et al.
Dyes and Pigments (2023) Vol. 218, pp. 111507-111507
Closed Access | Times Cited: 3
Denis A. Gazizov, Alexander S. Steparuk, Nadezhda S. Demina, et al.
Dyes and Pigments (2023) Vol. 218, pp. 111507-111507
Closed Access | Times Cited: 3
Triazines, Tetrazines, and Fused Ring Polyaza Systems
Marie‐Aude Hiebel, Franck Suzenet
Progress in heterocyclic chemistry (2019), pp. 505-531
Closed Access | Times Cited: 7
Marie‐Aude Hiebel, Franck Suzenet
Progress in heterocyclic chemistry (2019), pp. 505-531
Closed Access | Times Cited: 7
An alternative synthesis of 7-amino-6-nitro-substituted azolo[1,5-a]pyrimidines
Ilya I. Butorin, Olga A. Konovalova, Павел А. Слепухин, et al.
Mendeleev Communications (2024) Vol. 34, Iss. 5, pp. 706-708
Closed Access
Ilya I. Butorin, Olga A. Konovalova, Павел А. Слепухин, et al.
Mendeleev Communications (2024) Vol. 34, Iss. 5, pp. 706-708
Closed Access
Efficient Synthesis of Novel Triazolo[5,1-b]purines by Diacetoxyiodobenzene-Mediated Oxidative Cyclization of Schiff Bases
Artyom O. Neymash, Victor V. Fedotov, Evgeny N. Ulomsky, et al.
Reactions (2024) Vol. 5, Iss. 4, pp. 1089-1100
Open Access
Artyom O. Neymash, Victor V. Fedotov, Evgeny N. Ulomsky, et al.
Reactions (2024) Vol. 5, Iss. 4, pp. 1089-1100
Open Access
Triazines, tetrazines, and fused ring polyaza systems
Marie‐Aude Hiebel, Franck Suzenet
Progress in heterocyclic chemistry (2021), pp. 441-472
Closed Access | Times Cited: 3
Marie‐Aude Hiebel, Franck Suzenet
Progress in heterocyclic chemistry (2021), pp. 441-472
Closed Access | Times Cited: 3