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:

Substituent effect of substrates on cucurbit[8]uril-catalytic oxidation of aryl alcohols
Hang Cong, Zhaojie Li, Yong-Huan Wang, et al.
Journal of Molecular Catalysis A Chemical (2013) Vol. 374-375, pp. 32-38
Closed Access | Times Cited: 14

Showing 14 citing articles:

Cucurbiturils: from synthesis to high-affinity binding and catalysis
Khaleel I. Assaf, Werner M. Nau
Chemical Society Reviews (2014) Vol. 44, Iss. 2, pp. 394-418
Open Access | Times Cited: 1214

Organic–inorganic supramolecular solid catalyst boosts organic reactions in water
Pilar Garcı́a Garcı́a, José María Moreno, Urbano Díaz, et al.
Nature Communications (2016) Vol. 7, Iss. 1
Open Access | Times Cited: 52

Enhanced Performance of Metal- and Additive-Free Pyridinium-Based Photocatalysts for Selective Aerobic Oxidation: The Role of Anion Exchange in Boosting Reactive Oxygen Species Generation
Jing‐Wang Cui, Shuai Ma, C. N. R. Rao, et al.
ACS Sustainable Chemistry & Engineering (2022) Vol. 10, Iss. 6, pp. 2148-2157
Closed Access | Times Cited: 13

Chemo-selective oxidation of hydroxybenzyl alcohols with IBX in the presence of hemicucurbit[6]uril
Hang Cong, Takehiko Yamato, Zhu Tao
New Journal of Chemistry (2013) Vol. 37, Iss. 11, pp. 3778-3778
Closed Access | Times Cited: 25

Remarkable Acceleration of Benzimidazole Synthesis and Cyanosilylation Reactions in a Supramolecular Solid Catalyst
Sergio Rojas‐Buzo, Pilar Garcı́a Garcı́a, Avelino Corma
ChemCatChem (2016) Vol. 9, Iss. 6, pp. 997-1004
Closed Access | Times Cited: 16

IBX Oxidation of Benzenedimethanols in the Presence of Cucurbit[8]uril
Hang Cong, Qiuju Chen, Qing-Xia Geng, et al.
Chinese Journal of Chemistry (2015) Vol. 33, Iss. 5, pp. 545-549
Closed Access | Times Cited: 8

Synthesis of dibenzo[a,j]phenazine compounds using hemicucurbit[6]uril‐catalyzed oxidative dimerization of 2‐arylamines
Heng Li, Yu Juan, Qingmei Ge, et al.
ChemCatChem (2020) Vol. 12, Iss. 22, pp. 5727-5732
Closed Access | Times Cited: 8

Advancement in supramolecular control of organic reactivity induced by cucurbit[n]urils
Kevin Droguett, Guillermo E. Quintero, José G. Santos, et al.
Journal of Inclusion Phenomena and Macrocyclic Chemistry (2022) Vol. 103, Iss. 1-2, pp. 1-20
Closed Access | Times Cited: 5

Modification of carbon paste electrode with cucurbit[8]uril and its recognition to phenols
Hang Cong, Zhaojie Li, Qing-Xia Geng, et al.
Journal of Inclusion Phenomena and Macrocyclic Chemistry (2015) Vol. 81, Iss. 3-4, pp. 493-498
Closed Access | Times Cited: 5

2-Iodoxybenzenesulfonic Acid-Catalysed oxidation of Primary and Secondary Alcohols with Oxone in Cetyl Trimethylammonium Bromide Micelles at Room Temperature
Yangyang Liu, Boliang Wang
Journal of Chemical Research (2014) Vol. 38, Iss. 7, pp. 427-431
Closed Access | Times Cited: 5

Oxidations with Iodine(V) Compounds – From Stoichiometric Compounds to Catalysts
Frederic Ballaschk, Stefan F. Kirsch
(2022), pp. 299-334
Closed Access | Times Cited: 4

Selective oxidation of benzyl alcohols photocatalyzed by asymmetric cobalt thioporphyrazine supported on alumina
Wenyao Zhou, Rongjiao Tan, Changjun Yang, et al.
Molecular Catalysis (2024) Vol. 569, pp. 114608-114608
Closed Access

Cucurbiturils as Reaction Vessels
Héctor Barbero, Eric Masson
The Royal Society of Chemistry eBooks (2019), pp. 86-120
Closed Access | Times Cited: 2

The Use of Cucurbit[ n ]urils as Organic Nanoreactors
Brian D. Wagner
Elsevier eBooks (2016), pp. 43-84
Closed Access | Times Cited: 1

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