Open Access Helper

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:

Showing 1-25 of 32 citing articles:

Synthesis, antidiabetic activity and molecular docking study of rhodanine-substitued spirooxindole pyrrolidine derivatives as novel α-amylase inhibitors
Amani Toumi, Sarra Boudriga, Khaled Hamden, et al.
Bioorganic Chemistry (2020) Vol. 106, pp. 104507-104507
Open Access | Times Cited: 97
Pyrrolo[2,1-a]isoquinoline scaffolds for developing anti-cancer agents
Leidy J. García Maza, Arturo René Mendoza Salgado, Vladímir V. Kouznetsov, et al.
RSC Advances (2024) Vol. 14, Iss. 3, pp. 1710-1728
Open Access | Times Cited: 9
Engaging Isatins in Multicomponent Reactions (MCRs) – Easy Access to Structural Diversity
Pedro Brandão, Carolina S. Marques, Elisabete P. Carreiro, et al.
The Chemical Record (2021) Vol. 21, Iss. 4, pp. 924-1037
Open Access | Times Cited: 43
Diversity-Oriented Synthesis of Spiropyrrolo[1,2-a]isoquinoline Derivatives via Diastereoselective and Regiodivergent Three-Component 1,3-Dipolar Cycloaddition Reactions: In Vitro and in Vivo Evaluation of the Antidiabetic Activity of Rhodanine Analogues
Amani Toumi, Sarra Boudriga, Khaled Hamden, et al.
The Journal of Organic Chemistry (2021) Vol. 86, Iss. 19, pp. 13420-13445
Closed Access | Times Cited: 35
Stereoselective synthesis of fused-, spiro- and bridged heterocycles via cyclization of isoquinolinium salts: a recent update
Suven Das
Organic & Biomolecular Chemistry (2022) Vol. 20, Iss. 9, pp. 1838-1868
Closed Access | Times Cited: 25
Construction of 3,4-Dihydroquinolone Derivatives through Pd-Catalyzed [4+2] Cycloaddition of Vinyl Benzoxazinanones with α-Alkylidene Succinimides
Ting-Ting Yu, Peng-Ting Huang, Ben‐Hong Chen, et al.
The Journal of Organic Chemistry (2024) Vol. 89, Iss. 5, pp. 3279-3291
Closed Access | Times Cited: 4
Condensation-Based Methods for the C–H Bond Functionalization of Amines
Daniel Seidel, Weijie Chen
Synthesis (2021) Vol. 53, Iss. 21, pp. 3869-3908
Open Access | Times Cited: 25
New spiropyrrolothiazole derivatives bearing an oxazolone moiety as potential antidiabetic agent: Design, synthesis, crystal structure, Hirshfeld surface analysis, ADME and molecular docking studies
Manel Ben Hammouda, Sarra Boudriga, Khaled Hamden, et al.
Journal of Molecular Structure (2022) Vol. 1254, pp. 132398-132398
Closed Access | Times Cited: 17
Three-Component Access to Functionalized Spiropyrrolidine Heterocyclic Scaffolds and Their Cholinesterase Inhibitory Activity
Sarra Boudriga, Saoussen Haddad, Vikneswaran Murugaiyah, et al.
Molecules (2020) Vol. 25, Iss. 8, pp. 1963-1963
Open Access | Times Cited: 27
Substrate‐Controlled Regioselectivity Switch in a Three‐Component 1,3‐Dipolar Cycloaddition Reaction to Access 3,3′‐Pyrrolidinyl‐Spirooxindoles Derivatives
Kai‐Kai Wang, Yan‐Li Li, Rongxiang Chen, et al.
Advanced Synthesis & Catalysis (2022) Vol. 364, Iss. 12, pp. 2047-2052
Closed Access | Times Cited: 15
Antimicrobial Activity and In Silico Molecular Docking Studies of Pentacyclic Spiro[oxindole-2,3′-pyrrolidines] Tethered with Succinimide Scaffolds
Sonia Askri, Amal Dbeibia, Chadlia Mchiri, et al.
Applied Sciences (2021) Vol. 12, Iss. 1, pp. 360-360
Open Access | Times Cited: 20
A Review on the Synthesis and Applications of α‐Alkylidene Succinimides
Sakkani Nagaraju, Santosh K. Nanda
Asian Journal of Organic Chemistry (2022) Vol. 11, Iss. 4
Closed Access | Times Cited: 13
Brønsted Base‐Catalyzed Tandem [2+4] Annulation/Tautomerization/Aromatization Reaction of α‐Alkylidene Succinimides with 5‐Alkenyl Thiazolones
Chunhao Yuan, Huimin Yang, Qi Gong, et al.
Advanced Synthesis & Catalysis (2021) Vol. 363, Iss. 13, pp. 3336-3347
Closed Access | Times Cited: 14
Recent synthetic strategies of spiro-azetidin-2-one, -pyrrolidine, -indol(one) and -pyran derivatives-a review
Mohammed B. Alshammari, Ashraf A. Aly, Akil Ahmad, et al.
RSC Advances (2023) Vol. 13, Iss. 46, pp. 32786-32823
Open Access | Times Cited: 5
Synthesis of pyrrolidinedione-fused hexahydropyrrolo[2,1-a]isoquinolines via three-component [3 + 2] cycloaddition followed by one-pot N-allylation and intramolecular Heck reactions
Xiaoming Ma, Suzhi Meng, Xiaofeng Zhang, et al.
Beilstein Journal of Organic Chemistry (2020) Vol. 16, pp. 1225-1233
Open Access | Times Cited: 12
Enantioselective Organocatalyzed Mannich Reaction between Benzothiazolimines and α‐Benzylidene Succinimides for the Preparation of Chiral Benzothiazol Succinimides
Chen‐Yi Li, Min Xiang, Jian Zhang, et al.
Asian Journal of Organic Chemistry (2022) Vol. 11, Iss. 8
Closed Access | Times Cited: 8
Chiral Phosphine Catalyzed Allylic Alkylation of Benzylidene Succinimides with Morita–Baylis–Hillman Carbonates
Chang Liu, Jianwei Sun, Pengfei Li
Molecules (2023) Vol. 28, Iss. 6, pp. 2825-2825
Open Access | Times Cited: 4
One-pot synthesis, structural study, in silico and in vitro anticancer evaluation of spiropyrrolidine oxindoles obtained by the 3-CR of isatin, benzyl amine and a thiazolo[3,2-a]indole derivative
C.B. Meenakshy, Athul Sudheendranath, Noble V. Thomas, et al.
Journal of Molecular Structure (2023) Vol. 1298, pp. 137026-137026
Closed Access | Times Cited: 4
A base-catalyzed domino reaction between isoindigos and α-alkylidene succinimides—convenient preparation of highly steric bispirooxindoles
Chenyi Li, Min Xiang, Xiang‐Jia Song, et al.
Organic & Biomolecular Chemistry (2020) Vol. 18, Iss. 46, pp. 9511-9515
Closed Access | Times Cited: 11
Stereoselective Synthesis of Dispirooxindoles Incorporating Pyrrolo[2,1-a]isoquinoline via [3+2] Cycloaddition of Azomethine Ylides with a Thiazolo[3,2-a]indole Dipolarophile
Ani Deepthi, Noble V. Thomas, C.B. Meenakshy, et al.
Synthesis (2022) Vol. 54, Iss. 12, pp. 2885-2893
Closed Access | Times Cited: 7
Phosphine-Catalyzed [4 + 1] Annulation of β’-Acetoxy Allenoate with α-Alkylidene Succinimides: Access to Functionalized Spirosuccinimide Derivatives
Chunjie Ni, Zhanhang Liang, Xiaojuan Xu, et al.
The Journal of Organic Chemistry (2024) Vol. 89, Iss. 22, pp. 16711-16720
Closed Access | Times Cited: 1
Stereoselective synthesis of dispiroindano pyrrolidines by the [3 + 2] cycloaddition of thiazolo[3,2‐a]indole tethered dipolarophile with azomethine ylides
Noble V. Thomas, Vidya Sathi, Ani Deepthi
Journal of Heterocyclic Chemistry (2022) Vol. 59, Iss. 8, pp. 1407-1416
Closed Access | Times Cited: 6
Recent Progress on the [3+2] Cycloaddition Route for the Synthesis of All-Carbon Quaternary Stereocentres
Ani Deepthi, Maneesh Mohan, Meenakshy C. Balachandran
SynOpen (2022) Vol. 06, Iss. 04, pp. 270-285
Open Access | Times Cited: 5
Spirocyclization and Michael addition of 3-benzylidene succinimides: route to spirocyclopentapyrrolidine-tetraones and benzylidene N-arylpyrrolidine-diones
Pooja Dahiya, Anoop Yadav, Rama Krishna Peddinti
Organic & Biomolecular Chemistry (2023) Vol. 21, Iss. 46, pp. 9192-9199
Closed Access | Times Cited: 2
Crystal structure of (1′S,2′S,3S)-1′-benzoyl-2′-(4-methoxyphenyl)-1-methyl-2′,5′,6′,10b′-tetrahydro-1′H-spiro[indoline-3,3′-pyrrolo[2,1-a]isoquinolin]-2-one
Janet Priyavathani Selvaraj, S. Stella Mary, Jyoti Boruah Dhruba, et al.
Acta Crystallographica Section E Crystallographic Communications (2020) Vol. 76, Iss. 10, pp. 1548-1550
Open Access | Times Cited: 3
Page 1 - Next Page

Scroll to top