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:

A TfOH‐Catalyzed Multicomponent Reaction of Propargylic Alcohols, Sulfonamides and Aldehydes for the Synthesis of Acyclic α‐Arylidene β‐Aminoketones
Tiantian Li, Qinglin Zhang, Zhihai Wang, et al.
Asian Journal of Organic Chemistry (2023) Vol. 12, Iss. 4
Closed Access | Times Cited: 5

Showing 5 citing articles:

Recent Progress in Application of Propargylic Alcohols in Organic Syntheses
Fatemeh Doraghi, Amir Mohammad Mahdavian, Somaye Karimian, et al.
Advanced Synthesis & Catalysis (2023) Vol. 365, Iss. 18, pp. 2991-3019
Closed Access | Times Cited: 15

Silver(I)-catalyzed and DBU-promoted isomerization/addition of propargyl alcohols to amines to access β-aminoketones
Jialing Kang, Yifan Liu, Ronghai Cui, et al.
Tetrahedron Letters (2024) Vol. 145, pp. 155163-155163
Closed Access | Times Cited: 1

Synthesis of primary propargylic alcohols from terminal alkynes using rongalite as the C1 unit
Miao Wang, Shan Jiang, Xinxin Lu, et al.
Organic & Biomolecular Chemistry (2023) Vol. 21, Iss. 29, pp. 5949-5952
Closed Access | Times Cited: 3

Regioselective Synthesis of Isoxazoles from Propargylic Alcohols via In‐situ‐formed α‐Iodo Enones/Enals
Yang Hong, Jiaming Chen, Shuai He, et al.
Asian Journal of Organic Chemistry (2023) Vol. 13, Iss. 3
Closed Access | Times Cited: 2

The Meyer–Schuster Rearrangement
Giovanni Vidari, Debora Chiodi, Alessio Porta, et al.
Organic reactions (2024), pp. 411-730
Closed Access

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