OpenAlex Citation Counts

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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:

An insight into the advanced synthetic recipes to access ubiquitous indole heterocycles
Basavarajaiah Suliphuldevara Mathada, Nagesh Gunavanthrao Yernale, N. Jeelan Basha, et al.
Tetrahedron Letters (2021) Vol. 85, pp. 153458-153458
Closed Access | Times Cited: 57

Showing 26-50 of 57 citing articles:

Indole frameworks via transition-metal-free annulation: a current perspective
Suven Das
New Journal of Chemistry (2023) Vol. 47, Iss. 29, pp. 13729-13775
Closed Access | Times Cited: 10

Synthesis, Spectral Analysis, DFT Calculations, in Vitro Screening, and Molecular Docking of New Metal Complexes with Quinoline and Isoniazid Schiff Base as Antimicrobial and Antioxidant Agents
R. Nalini, Nagesh Gunavanthrao Yernale, J. Mohammad, et al.
Polycyclic aromatic compounds (2023) Vol. 44, Iss. 8, pp. 5439-5459
Closed Access | Times Cited: 10

Review on Contemporary Synthetic Recipes to Access Versatile Coumarin Heterocycles
S. M. Basavarajaiah, Nagesh Gunavanthrao Yernale, Munianjinappa Punith Kumar, et al.
Polycyclic aromatic compounds (2023) Vol. 44, Iss. 5, pp. 3576-3600
Closed Access | Times Cited: 9

In silico, in vitro and docking exploration for some novel coordination complexes derived from bioactive indole moiety
Nagesh Gunavanthrao Yernale, Basavarajaiah Suliphuldevara Mathada, Giridhar Baburao, et al.
Journal of Molecular Structure (2023) Vol. 1294, pp. 136512-136512
Closed Access | Times Cited: 9

Discovery of Novel Isatin Encompassing Oxadiazoles as Potential Inhibitors against New Delhi Metallo-β-lactamase-1: Synthesis, Spectral Analysis, Antimicrobial, and Molecular Modeling Studies
B. Sridhar, Nagesh Gunavanthrao Yernale, Prashantha Karunakar, et al.
Russian Journal of Bioorganic Chemistry (2024) Vol. 50, Iss. 4, pp. 1376-1389
Closed Access | Times Cited: 3

Synthesis of 3-arylamino-2-polyhydroxyalkyl-substituted indoles from unprotected saccharides and anilines
Jilai Wu, Likai Zhou, Song Xie, et al.
Green Chemistry (2024) Vol. 26, Iss. 4, pp. 1883-1888
Closed Access | Times Cited: 2

Design, synthesis and biological evaluation of novel isoniazid hybrids
R. Nalini, S. M. Basavarajaiah, Nagesh Gunavanthrao Yernale, et al.
Journal of the Indian Chemical Society (2021) Vol. 99, Iss. 1, pp. 100273-100273
Closed Access | Times Cited: 17

Synthesis, Characterization and Biological Activity of ONO Donor Schiff Base and its Metal Complexes
R. Nalini, S. M. Basavarajaiah, Nagesh Gunavanthrao Yernale, et al.
Asian Journal of Chemistry (2022) Vol. 34, Iss. 2, pp. 389-394
Open Access | Times Cited: 12

Biphasic Dose‐Dependent G0/G1 and G2/M Cell‐Cycle Arrest by Synthetic 2,3‐Arylpyridylindole Derivatives in A549 Lung Cancer Cells
Pongtai Chaiputtanapun, Kriengsak Lirdprapamongkol, Bongkotrat Thanaussavadate, et al.
ChemMedChem (2022) Vol. 17, Iss. 14
Closed Access | Times Cited: 9

A Tandem Madelung Indole Synthesis Mediated by a LiN(SiMe3)2/CsF System
Ruyuan Ma, Yan‐En Wang, Dan Xiong, et al.
Organic Letters (2023) Vol. 25, Iss. 41, pp. 7557-7561
Closed Access | Times Cited: 5

Synthesis of Indoles by Palladium-Catalyzed Reductive Cyclization of β-Nitrostyrenes with Phenyl Formate as a CO Surrogate
Francesco Ferretti, Manar Ahmed Fouad, Fabio Ragaini
Catalysts (2022) Vol. 12, Iss. 1, pp. 106-106
Open Access | Times Cited: 8

Rhodium-catalyzed annulation for the construction of indole core: An update
Suven Das, Arpita Dutta
Tetrahedron (2023) Vol. 146, pp. 133633-133633
Closed Access | Times Cited: 4

Rapid access to diverse indoles by addition/SNAr with Grignard reagents and 2-fluorophenyl acetonitriles
Yuanyun Gu, Yaxin Feng, Baotong Huang, et al.
Green Synthesis and Catalysis (2024)
Open Access | Times Cited: 1

Synthesis of Indoles via Domino Reactions of 2-Methoxytoluene and Nitriles
Song Kou, Jingqian Huo, Ying Wang, et al.
The Journal of Organic Chemistry (2022) Vol. 88, Iss. 8, pp. 5147-5152
Closed Access | Times Cited: 5

Antimicrobial Activity of N‐Substituted Derivatives of 5‐Chloro‐2,3‐ Diphenyl Indole
Mamdouh A. Sofan, Fawzia Z. El‐Ablack, Aya I. Elsayed
ChemistrySelect (2023) Vol. 8, Iss. 46
Closed Access | Times Cited: 2

Copper‐Catalyzed One‐Pot Arylation and Cyclization of Diaryliodonium Salts Derived from o‐Iodoanilines for Indolo[2,3‐b]indoles Syntheses
Mi-Seon Choi, Manish Kumar Mehra, Chung Whan Lee
European Journal of Organic Chemistry (2022) Vol. 26, Iss. 4
Closed Access | Times Cited: 4

Update on Thiopyran Fused Heterocycle Synthesis (2013-2024)
Ani Deepthi, Sruthi Sudheendran Leena, Devika Krishnan
Organic & Biomolecular Chemistry (2024) Vol. 22, Iss. 28, pp. 5676-5717
Closed Access

Synthesis of Indole‐2‐carboxylates via Condensation of Nitroacetic Esters and 2‐Dimethylbenzaldehydes
Elvira R. Zaitseva, Dmitrii S. Ivanov, Надежда С. Балеева, et al.
ChemistrySelect (2023) Vol. 8, Iss. 42
Closed Access

Studies on molecular structure, UV visible, NMR and HOMO-LUMO of indole derivative using DFT calculation
Sulochana Devar, Vijayalaxmi Gangadharmath, N G Yernale, et al.
AIP conference proceedings (2023) Vol. 2931, pp. 040038-040038
Closed Access

Bilgisayar Destekli İlaç Tasarımı ve Tasarımın Ticari Ürün Örneklerine Kısa Bir Bakış
YASEMİN KEŞKEK KARABULUT, Zeynep Şilan TURHAN
Özgür Yayınları eBooks (2023)
Open Access

Yeşil Sentez: Nano Partiküller ve Potansiyel Uygulama Alanları
Aybek Yiğit, Necdet Karakoyun, Zeynep Şilan TURHAN
Özgür Yayınları eBooks (2023)
Open Access

Nanotechnology and Current Applications in Biotechnology
Pınar Bozbeyoğlu, Pelin Keçeci
Özgür Yayınları eBooks (2023)
Open Access

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