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.

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Showing 13 citing articles:

Recent Advances in Organocatalytic Asymmetric Michael Addition Reactions to α, β‐Unsaturated Nitroolefins
Tapaswini Das, Seetaram Mohapatra, Nilima Priyadarsini Mishra, et al.
ChemistrySelect (2021) Vol. 6, Iss. 15, pp. 3745-3781
Closed Access | Times Cited: 54

Stereoselective Domino Reactions in the Synthesis of Spiro Compounds
Maurizio Benaglia, Sandro J. Greco, Regina Westphal, et al.
Synthesis (2022) Vol. 54, Iss. 13, pp. 2927-2975
Open Access | Times Cited: 29

Enantioselective Synthesis of Spiro[cyclopentane-1,3′-oxindole] Scaffolds with Five Consecutive Stereocenters
Qiliang Luo, Tao Mao, Yao Luo, et al.
Organic Letters (2024) Vol. 26, Iss. 30, pp. 6402-6406
Closed Access | Times Cited: 3

Squaramide Catalyzed Asymmetric Synthesis of Five‐ and Six‐Membered Rings
Anup Biswas, Avisek Ghosh, Rajat Shankhdhar, et al.
Asian Journal of Organic Chemistry (2021) Vol. 10, Iss. 6, pp. 1345-1376
Closed Access | Times Cited: 21

Palladium-catalysed 5-endo-trig allylic (hetero)arylation
Bara Singh, Siddheshwar K. Bankar, Ketan Kumar, et al.
Chemical Science (2020) Vol. 11, Iss. 19, pp. 4948-4953
Open Access | Times Cited: 21

Enantioselective Construction of Spirooxindole-Fused Cyclopentanes
Vojtěch Dočekal, Andrea Vopálenská, Pavel Měrka, et al.
The Journal of Organic Chemistry (2021) Vol. 86, Iss. 18, pp. 12623-12643
Closed Access | Times Cited: 19

1,2-trans-Diaminocyclohexane (DACH) in Asymmetric Catalysis: Nearing Fifty Years of Faithful Service and Counting
Stephen Hanessian, Akash Mishra
Synthesis (2024) Vol. 56, Iss. 18, pp. 2747-2885
Closed Access | Times Cited: 2

The Molecular Diversity Scope of Oxindole Derivatives in Organic Synthesis
Ghodsi Mohammadi Ziarani, Fatemeh Javadi, Fatemeh Mohajer
Current Organic Chemistry (2021) Vol. 25, Iss. 7, pp. 779-818
Closed Access | Times Cited: 16

Tandem 1,6-addition/cyclopropanation/rearrangement reaction of vinylogous para-quinone methides with 3-chlorooxindoles: construction of vicinal quaternary carbon centers
Yuan Pan, Weiwu Ren, Zhanhao Zhang, et al.
Organic Chemistry Frontiers (2022) Vol. 9, Iss. 14, pp. 3697-3708
Closed Access | Times Cited: 6

Asymmetric Sequential Michael Addition and Cyclization Reactions of 2-(2-Nitrovinyl)phenols Catalyzed by Bifunctional Amino-Squaramides
Radovan Šebesta, Eva Veverková, Pavlína Molnosiová
SynOpen (2021) Vol. 05, Iss. 04, pp. 278-284
Open Access | Times Cited: 6

A consecutive synthesis of spirocyclopentanes from 2,4-dioxo-arylbutanoates, malononitrile and vicinal dicarbonyl compounds
Azadeh Parhami, Issa Yavari
Synthetic Communications (2021) Vol. 51, Iss. 18, pp. 2847-2852
Closed Access | Times Cited: 3

Enantioselective Synthesis of Spirocyclopentane Oxindoles Bearing Five Consecutive Stereocenters through Secondary Amine‐Catalyzed [3+2] Cycloaddition
Jingwei Zhou, Ben‐Hong Chen, Feng‐Hua Zhang, et al.
European Journal of Organic Chemistry (2022) Vol. 2022, Iss. 20
Closed Access | Times Cited: 1

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