
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:
Molecular diversity of TEMPO-mediated cycloaddition of ketohydrazones and 3-phenacylideneoxindoles
Rong Ye, Jing Sun, Ying Han, et al.
New Journal of Chemistry (2021) Vol. 45, Iss. 11, pp. 5075-5080
Closed Access | Times Cited: 16
Rong Ye, Jing Sun, Ying Han, et al.
New Journal of Chemistry (2021) Vol. 45, Iss. 11, pp. 5075-5080
Closed Access | Times Cited: 16
Showing 16 citing articles:
Update on the Synthesis of N‐Heterocycles via Cyclization of Hydrazones (2017–2021)
Yunhe Lv, Jianping Meng, Chen Li, et al.
Advanced Synthesis & Catalysis (2021) Vol. 363, Iss. 23, pp. 5235-5265
Closed Access | Times Cited: 59
Yunhe Lv, Jianping Meng, Chen Li, et al.
Advanced Synthesis & Catalysis (2021) Vol. 363, Iss. 23, pp. 5235-5265
Closed Access | Times Cited: 59
Regioselective Synthesis of Pyrazolo[1,5-a]pyridine via TEMPO-Mediated [3 + 2] Annulation–Aromatization ofN-Aminopyridines and α,β-Unsaturated Compounds
Amu Wang, Yazhou Liu, Zhongke Shen, et al.
Organic Letters (2022) Vol. 24, Iss. 7, pp. 1454-1459
Closed Access | Times Cited: 23
Amu Wang, Yazhou Liu, Zhongke Shen, et al.
Organic Letters (2022) Vol. 24, Iss. 7, pp. 1454-1459
Closed Access | Times Cited: 23
Bifunctional TEMPO-based catalysis boosts luminol electrochemiluminescence for cholesterol sensing
Haidong Li, Guangyue Zhao, Yuxin Yang, et al.
Sensors and Actuators B Chemical (2023) Vol. 403, pp. 135186-135186
Closed Access | Times Cited: 11
Haidong Li, Guangyue Zhao, Yuxin Yang, et al.
Sensors and Actuators B Chemical (2023) Vol. 403, pp. 135186-135186
Closed Access | Times Cited: 11
Aza-Diels-Alder reaction of both electron-deficient azoalkenes with electron-deficient 3-phencaylideneoxindoles and 3-aryliminooxindol-2-ones
Wen‐Jing Shi, Jing Sun, Chao‐Guo Yan
Green Synthesis and Catalysis (2021) Vol. 2, Iss. 4, pp. 362-366
Open Access | Times Cited: 18
Wen‐Jing Shi, Jing Sun, Chao‐Guo Yan
Green Synthesis and Catalysis (2021) Vol. 2, Iss. 4, pp. 362-366
Open Access | Times Cited: 18
Multicomponent Reaction for Diastereoselective Synthesis of Spiro[carbazole-3,4′-pyrazoles] and Spiro[carbazole-3,4′-thiazoles]
Shao‐Cong Zhan, Ren-Jie Fang, Jing Sun, et al.
The Journal of Organic Chemistry (2021) Vol. 86, Iss. 13, pp. 8726-8741
Closed Access | Times Cited: 16
Shao‐Cong Zhan, Ren-Jie Fang, Jing Sun, et al.
The Journal of Organic Chemistry (2021) Vol. 86, Iss. 13, pp. 8726-8741
Closed Access | Times Cited: 16
Bright luminol electrochemiluminescence mediated by a simple TEMPO radical for visualized multiplex detection
Haidong Li, Guangyue Zhao, Yuxin Yang, et al.
Talanta (2024) Vol. 278, pp. 126530-126530
Closed Access | Times Cited: 2
Haidong Li, Guangyue Zhao, Yuxin Yang, et al.
Talanta (2024) Vol. 278, pp. 126530-126530
Closed Access | Times Cited: 2
Chemo- and Diastereoselective Synthesis of Spirooxindole-pyrazolines and Pyrazolones via P(NMe2)3-Mediated Substrate-Controlled Annulations of Azoalkenes with α-Dicarbonyl Compounds
Yunfeng Du, Yuefei Liu, Hongyu Guo, et al.
Organic Letters (2023) Vol. 25, Iss. 26, pp. 4776-4781
Closed Access | Times Cited: 6
Yunfeng Du, Yuefei Liu, Hongyu Guo, et al.
Organic Letters (2023) Vol. 25, Iss. 26, pp. 4776-4781
Closed Access | Times Cited: 6
Diaza-1,3-butadienes as Useful Intermediate in Heterocycles Synthesis
Jorge Heredia‐Moya, Daniel A. Zurita, José Eduardo Cadena-Cruz, et al.
Molecules (2022) Vol. 27, Iss. 19, pp. 6708-6708
Open Access | Times Cited: 7
Jorge Heredia‐Moya, Daniel A. Zurita, José Eduardo Cadena-Cruz, et al.
Molecules (2022) Vol. 27, Iss. 19, pp. 6708-6708
Open Access | Times Cited: 7
Efficient synthesis of polyfunctionalized carbazoles and pyrrolo[3,4-c]carbazoles via domino Diels–Alder reaction
Ren-Jie Fang, Yan Chen, Jing Sun, et al.
Beilstein Journal of Organic Chemistry (2021) Vol. 17, pp. 2425-2432
Open Access | Times Cited: 9
Ren-Jie Fang, Yan Chen, Jing Sun, et al.
Beilstein Journal of Organic Chemistry (2021) Vol. 17, pp. 2425-2432
Open Access | Times Cited: 9
DDQ dehydrogenative Diels–Alder reaction for the synthesis of functionalized spiro[carbazole-1,3′-indolines] and spiro[carbazole-1,5′-pyrimidines]
Shao‐Cong Zhan, Ren-Jie Fang, Ren‐Yin Yang, et al.
New Journal of Chemistry (2021) Vol. 45, Iss. 34, pp. 15423-15428
Closed Access | Times Cited: 8
Shao‐Cong Zhan, Ren-Jie Fang, Ren‐Yin Yang, et al.
New Journal of Chemistry (2021) Vol. 45, Iss. 34, pp. 15423-15428
Closed Access | Times Cited: 8
Copper-catalyzed multicomponent reactions for the efficient synthesis of diverse spirotetrahydrocarbazoles
Shao‐Cong Zhan, Ren-Jie Fang, Jing Sun, et al.
Beilstein Journal of Organic Chemistry (2022) Vol. 18, pp. 796-808
Open Access | Times Cited: 6
Shao‐Cong Zhan, Ren-Jie Fang, Jing Sun, et al.
Beilstein Journal of Organic Chemistry (2022) Vol. 18, pp. 796-808
Open Access | Times Cited: 6
3-Phenacylideneoxindoles in organic synthesis: Recent developments
Fatemeh Doraghi, Mohammad Javad Karimi, Bahareh Bari, et al.
Tetrahedron Letters (2023) Vol. 129, pp. 154725-154725
Closed Access | Times Cited: 3
Fatemeh Doraghi, Mohammad Javad Karimi, Bahareh Bari, et al.
Tetrahedron Letters (2023) Vol. 129, pp. 154725-154725
Closed Access | Times Cited: 3
Catalytic asymmetric [4 + 1] cycloaddition to synthesize chiral pyrazoline-spirooxindoles
Kaiqi Hu, Dong Zhang, Siyuan Wang, et al.
Organic Chemistry Frontiers (2023) Vol. 10, Iss. 10, pp. 2422-2428
Closed Access | Times Cited: 2
Kaiqi Hu, Dong Zhang, Siyuan Wang, et al.
Organic Chemistry Frontiers (2023) Vol. 10, Iss. 10, pp. 2422-2428
Closed Access | Times Cited: 2
Convenient Construction of Spiro[pyrazole‐4,1′‐pyrido[2,1‐a]isoquinoline] and Spiro[pyrazole‐4,4′‐pyrido[1,2‐a]quinoline] via Three‐Component Reaction
Hui‐Ling Fang, Jing Sun, Chao‐Guo Yan
ChemistrySelect (2021) Vol. 6, Iss. 39, pp. 10537-10541
Closed Access | Times Cited: 4
Hui‐Ling Fang, Jing Sun, Chao‐Guo Yan
ChemistrySelect (2021) Vol. 6, Iss. 39, pp. 10537-10541
Closed Access | Times Cited: 4
Convenient generation of 1,3-dipolar nitrilimines and [3 + 2] cycloaddition for the synthesis of spiro compounds
Mei-Jun Zhu, Rong Ye, Wen‐Jing Shi, et al.
Tetrahedron Letters (2022) Vol. 110, pp. 154186-154186
Closed Access | Times Cited: 2
Mei-Jun Zhu, Rong Ye, Wen‐Jing Shi, et al.
Tetrahedron Letters (2022) Vol. 110, pp. 154186-154186
Closed Access | Times Cited: 2
Domino Reaction for Synthesis of Spiro[pyrazole‐4,5′‐pyrrolo[3,4‐c]carbazoles] and Spiro[pyrrolo[3,4‐c]carbazole‐5,5′‐thiazoles]
Yan Chen, Jing Sun, Ying Han, et al.
Asian Journal of Organic Chemistry (2021) Vol. 10, Iss. 10, pp. 2632-2637
Closed Access
Yan Chen, Jing Sun, Ying Han, et al.
Asian Journal of Organic Chemistry (2021) Vol. 10, Iss. 10, pp. 2632-2637
Closed Access