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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:

Facile “on water” domino reactions for the expedient synthesis of 2H-thiopyrano[2,3-b]quinolines
Sundaravel Vivek Kumar, Shanmugam Muthusubramanian, Subbu Perumal
RSC Advances (2015) Vol. 5, Iss. 39, pp. 30826-30832
Closed Access | Times Cited: 17

Showing 17 citing articles:

Aldo‐X Bifunctional Building Blocks for the Synthesis of Heterocycles
Palanisamy Ravichandiran, Bingbing Lai, Yanlong Gu
The Chemical Record (2016) Vol. 17, Iss. 2, pp. 142-183
Closed Access | Times Cited: 49
Molecular Docking Study for Binding Affinity of 2H-thiopyrano[2,3-b]quinoline Derivatives against CB1a
Shivangi Sharma, Shivendra Singh
Interdisciplinary Perspectives on Infectious Diseases (2023) Vol. 2023, pp. 1-10
Open Access | Times Cited: 11
Exploration of Synthetic Potential of 2‐Chloro‐Quinoline‐3‐Carbaldehyde
Vipin Kumar, Shubham Sharma, Vaishali Vaishali, et al.
European Journal of Organic Chemistry (2024)
Closed Access | Times Cited: 2
A solvent- and catalyst-free domino reaction for the efficient synthesis of 3-arylthiazolidine-2-thiones under microwave irradiation
Sundaravel Vivek Kumar, Shanmugam Muthusubramanian, Subbu Perumal
RSC Advances (2015) Vol. 5, Iss. 110, pp. 90451-90456
Closed Access | Times Cited: 28
A facile stereoselective synthesis of dispiro-indeno pyrrolidine/pyrrolothiazole–thiochroman hybrids and evaluation of their antimycobacterial, anticancer and AchE inhibitory activities
Chelliah Bharkavi, Sundaravel Vivek Kumar, Mohamed Ashraf Ali, et al.
Bioorganic & Medicinal Chemistry (2016) Vol. 24, Iss. 22, pp. 5873-5883
Closed Access | Times Cited: 23
One-pot microwave assisted stereoselective synthesis of novel dihydro-2′H-spiro[indene-2,1′-pyrrolo-[3,4-c]pyrrole]-tetraones and evaluation of their antimycobacterial activity and inhibition of AChE
Chelliah Bharkavi, Sundaravel Vivek Kumar, Mohamed Ashraf Ali, et al.
Bioorganic & Medicinal Chemistry Letters (2017) Vol. 27, Iss. 14, pp. 3071-3075
Closed Access | Times Cited: 23
One-Pot Access to a Library of Dispiro Oxindole-pyrrolidine/pyrrolothiazole-thiochromane Hybrids via Three-Component 1,3-Dipolar Cycloaddition Reactions
Gandhi Uma Rani, Sundaravel Vivek Kumar, Chelliah Bharkavi, et al.
ACS Combinatorial Science (2016) Vol. 18, Iss. 6, pp. 337-342
Closed Access | Times Cited: 18
Synthesis of 1H‐Thiopyrano[4,3‐c]quinoline Scaffold via One‐pot Three‐component Cyclization
Abdolali Alizadeh, Reza Rezaiyehraad, Atefeh Roosta, et al.
ChemistrySelect (2019) Vol. 4, Iss. 41, pp. 12049-12052
Closed Access | Times Cited: 8
An efficient one pot three-component domino reaction for the synthesis of 1,3,4-trisubstituted pyrroles
Sundaravel Vivek Kumar, Sivasubramanian Muthusaravanan, Shanmugam Muthusubramanian, et al.
ChemistrySelect (2016) Vol. 1, Iss. 4, pp. 675-679
Closed Access | Times Cited: 7
Novel 1,2,4-Triazole- and Tetrazole-Containing 4H-Thiopyrano[2,3-b]quinolines: Synthesis Based on the Thio-Michael/aza-Morita–Baylis–Hillman Tandem Reaction and Investigation of Antiviral Activity
A. V. Khramchikhin, Mariya А. Skryl’nikova, Maxim Gureev, et al.
Molecules (2023) Vol. 28, Iss. 21, pp. 7427-7427
Open Access | Times Cited: 2
Expedient synthesis of nitrovinyl substituted bicyclo[2.2.2]octenone scaffolds
Shivangi Sharma, Ram Tilak Naganaboina, Rama Krishna Peddinti
RSC Advances (2015) Vol. 5, Iss. 121, pp. 100060-100069
Closed Access | Times Cited: 5
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
A Facile and Efficient Route for the Synthesis of Thiopyranoquinolines‐Fused Indole Moiety Using 2‐Chloroquinoline‐3‐carbaldehydes
Firouz Matloubi Moghaddam, Atiyeh Moafi, Ainaz Ziadkhani, et al.
ChemistrySelect (2019) Vol. 4, Iss. 40, pp. 11683-11686
Closed Access | Times Cited: 3
Synthesis of isomeric 4-(N-methyltetrazolylamino)-2-phenyl-4H-thiopyrano[2,3-b]quinoline-3-carbaldehydes and 4-hydroxy-2-phenyl-4H-thiopyrano[2,3-b]quinoline-3-carbaldehyde based on tandem thiol-Michael and (aza)-Morita–Baylis–Hillman reactions and an in vitro study of the activity of the obtained compounds against influenza virus
A. V. Khramchikhin, Mariya А. Skryl’nikova, Yuliya N. Pavlyukova, et al.
Chemistry of Heterocyclic Compounds (2022) Vol. 58, Iss. 4-5, pp. 267-270
Open Access | Times Cited: 2
Sodium sulphide promoted synthesis of fused quinoline at room temperature
Rashmi Singh, Vishal Prasad Sharma, Priyanka Yadav, et al.
Organic & Biomolecular Chemistry (2021) Vol. 19, Iss. 37, pp. 8108-8112
Closed Access | Times Cited: 2
A facile solvent-free three-component domino synthesis of novel 2,4-diaryl-5,6-dihydrobenzo[j][1,7]phenanthrolines
Shanmugavel Uma Maheswari, Sundaravel Vivek Kumar, Shanmugam Muthusubramanian, et al.
Molecular Diversity (2018) Vol. 23, Iss. 1, pp. 75-84
Closed Access | Times Cited: 1
ChemInform Abstract: Facile “On Water” Domino Reactions for the Expedient Synthesis of 2H‐Thiopyrano[2,3‐b]quinolines.
Sundaravel Vivek Kumar, Shanmugam Muthusubramanian, Subbu Perumal
ChemInform (2015) Vol. 46, Iss. 34
Closed Access
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