OpenAlex Citation Counts

OpenAlex Citations Logo

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 the three-component reaction of α-amino acids, dialkyl acetylenedicarboxylates and N-substituted maleimides
Liang Chen, Jing Sun, Ju Xie, et al.
Organic & Biomolecular Chemistry (2016) Vol. 14, Iss. 27, pp. 6497-6507
Closed Access | Times Cited: 27

Showing 1-25 of 27 citing articles:

Recent Advances on Diverse Decarboxylative Reactions of Amino Acids
Matiur Rahman, Anindita Mukherjee, Igor S. Коvalev, et al.
Advanced Synthesis & Catalysis (2018) Vol. 361, Iss. 10, pp. 2161-2214
Closed Access | Times Cited: 82

Diastereoselective construction of carbazole-based spirooxindoles via the Levy three-component reaction
Shao‐Cong Zhan, Jing Sun, Ruzhang Liu, et al.
Organic & Biomolecular Chemistry (2019) Vol. 18, Iss. 1, pp. 163-168
Closed Access | Times Cited: 49

TfOH-Catalyzed One-Pot Domino Reaction for Diastereoselective Synthesis of Polysubstituted Tetrahydrospiro[carbazole-1,3′-indoline]s
Ren‐Yin Yang, Jing Sun, Tao Yao, et al.
The Journal of Organic Chemistry (2017) Vol. 82, Iss. 24, pp. 13277-13287
Closed Access | Times Cited: 45

A [3+2] cycloaddition reaction for the synthesis of spiro[indoline-3,3′-pyrrolidines] and evaluation of cytotoxicity towards cancer cells
Ying Huang, Yixin Huang, Jing Sun, et al.
New Journal of Chemistry (2019) Vol. 43, Iss. 23, pp. 8903-8910
Closed Access | Times Cited: 31

Iodine-Promoted N–H/α,β-C(sp3)-Trifunctionalization of l-Proline: Access to 3,4-Dihydrobenzo[b][1,7]naphthyridines via Consecutive Decarboxylation/Ring Opening/Dicyclization
Xiao Geng, Can Wang, Peng Zhao, et al.
Organic Letters (2019) Vol. 21, Iss. 13, pp. 4939-4943
Closed Access | Times Cited: 30

Convenient construction of spiro[indoline-3,5'-pyrrolo[3,4-c]carbazole] and spiro[indene-2,5'-pyrrolo[3,4-c]carbazole] via acid-catalyzed Diels-Alder reaction
Yan Chen, Jing Sun, Chao‐Guo Yan
Chinese Chemical Letters (2020) Vol. 32, Iss. 3, pp. 1253-1256
Closed Access | Times Cited: 28

1,3-Indanedione: An versatile building block
Chao‐Guo Yan
Green Synthesis and Catalysis (2022) Vol. 4, Iss. 2, pp. 78-88
Open Access | Times Cited: 12

Selective synthesis of tetrahydroimidazo[1,2-a]pyridine and pyrrolidine derivatives via a one-pot two-step reaction
Yu Zhang, Jing Sun, Guo‐Liang Shen, et al.
Organic & Biomolecular Chemistry (2017) Vol. 15, Iss. 38, pp. 8072-8077
Closed Access | Times Cited: 17

Generation of New 1,3‐Dipolar Azomethine Ylide via Reaction of Ethyl Glycinate with Dialkyl But‐2‐ynedioate and Tandem 1,3‐Dipolar Cycloaddition Reaction
Ying Huang, Jing Sun, Chao‐Guo Yan
ChemistrySelect (2017) Vol. 2, Iss. 32, pp. 10496-10500
Closed Access | Times Cited: 13

Iodine promoted annulation reaction for selective construction of Spiro[indene-2,1′-pyrido[4,3-b]indole] and Benzo[5,6]pyrrolo[3′,2': 3,4]cyclohepta[1,2-b]indole
Lingyun Zhu, Jing Sun, Dan Liu, et al.
Tetrahedron (2024) Vol. 159, pp. 134026-134026
Closed Access | Times Cited: 1

Straightforward Synthesis of Succinimide-Fused Pyrrolizidines by A Three-Component Reaction of α-Diketone, Amino Acid, and Maleimide
Hua Zhao, Hongbin Zhai, Peng Shen, et al.
Synthesis (2020) Vol. 53, Iss. 07, pp. 1262-1270
Closed Access | Times Cited: 9

Synthesis of bridgehead-azacycles via dual C–N/C–C annulation of α-amino acids, aminals and maleimides
Nagender Thadem, Manda Rajesh, Harikrishna Balaboina, et al.
Organic & Biomolecular Chemistry (2022) Vol. 20, Iss. 32, pp. 6368-6383
Closed Access | Times Cited: 6

Convenient construction of polycyclic architectures via multicomponent reaction of amino acids, dialkyl but-2-ynedioates and 2-(o-hydroxyarylidene)-1,3-indanediones
Xueyan Liu, Jing Sun, Chao‐Guo Yan
New Journal of Chemistry (2022) Vol. 46, Iss. 24, pp. 11877-11882
Closed Access | Times Cited: 6

1,3-Dipolar cycloadditions with azomethine ylide species generated from aminocyclopropanes
Andrzej Wolan, Justyna A. Kowalska-Six, Holisoa Rajérison, et al.
Tetrahedron (2018) Vol. 74, Iss. 38, pp. 5248-5257
Open Access | Times Cited: 6

Microwave Irradiation Tandem Hydroamination and Oxidative Cyclization of Natural Amino Acids with Diethyl Acetylenedicarboxylate for Functionalized Pyrrole Derivatives
Ji-Sen Li, Wenwen Duan, Xiaoxia Pan, et al.
ChemistrySelect (2019) Vol. 4, Iss. 12, pp. 3281-3285
Closed Access | Times Cited: 6

Three-Component Reaction for Efficient Synthesis of Functionalized Spiro[cyclopentane-1,3'-indolines]
Weiqing Ma, Ying Han, Jin Sun, et al.
Chinese Journal of Organic Chemistry (2021) Vol. 41, Iss. 8, pp. 3180-3180
Open Access | Times Cited: 6

A diastereoselective synthesis of functionalized spiropyrrolizidine-linked rhodanines
Issa Yavari, Sara Sheikhi, Zohreh Taheri, et al.
Monatshefte für Chemie - Chemical Monthly (2019) Vol. 150, Iss. 10, pp. 1825-1831
Closed Access | Times Cited: 5

Molecular diversity of the base-promoted reaction of phenacylmalononitriles with dialkyl but-2-ynedioates
Hui Zheng, Ying Han, Jing Sun, et al.
Beilstein Journal of Organic Chemistry (2022) Vol. 18, pp. 991-998
Open Access | Times Cited: 2

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

The Solid-State Structures of Cyclic NH Carboximides
R. A. Aitken, Dheirya K. Sonecha
Crystals (2020) Vol. 10, Iss. 7, pp. 606-606
Open Access | Times Cited: 2

(3+2) Cycloaddition reactions in the synthesis of C(4)–N(5)-condensed tetrahydropyrrolo[3,4-c]pyrrole-1,3-diones (microreview)
С. М. Медведева, Х. С. Шихалиев
Chemistry of Heterocyclic Compounds (2016) Vol. 52, Iss. 9, pp. 687-689
Closed Access | Times Cited: 1

Page 1 - Next Page

Scroll to top