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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:

Turning Cucurbit[8]uril into a Supramolecular Nanoreactor for Asymmetric Catalysis
Lifei Zheng, Silvia Sonzini, Masyitha Ambarwati, et al.
Angewandte Chemie International Edition (2015) Vol. 54, Iss. 44, pp. 13007-13011
Open Access | Times Cited: 71

Showing 1-25 of 71 citing articles:

Catalytic Organic Reactions in Water toward Sustainable Society
Taku Kitanosono, K. Masuda, Pengyu Xu, et al.
Chemical Reviews (2017) Vol. 118, Iss. 2, pp. 679-746
Closed Access | Times Cited: 632
Molecular Recognition in Water Using Macrocyclic Synthetic Receptors
Luis Escobar, Pablo Ballester
Chemical Reviews (2021) Vol. 121, Iss. 4, pp. 2445-2514
Closed Access | Times Cited: 241
Bioinspired Framework Catalysts: From Enzyme Immobilization to Biomimetic Catalysis
Kunyu Wang, Jiaqi Zhang, Yu‐Chuan Hsu, et al.
Chemical Reviews (2023) Vol. 123, Iss. 9, pp. 5347-5420
Open Access | Times Cited: 167
Confinement Effects in Catalysis Using Well-Defined Materials and Cages
Valentinos Mouarrawis, Raoul Plessius, Jarl Ivar van der Vlugt, et al.
Frontiers in Chemistry (2018) Vol. 6
Open Access | Times Cited: 157
Self-Assembled Single-Walled Metal-Helical Nanotube (M-HN): Creation of Efficient Supramolecular Catalysts for Asymmetric Reaction
Jian Jiang, Yan Meng, Li Zhang, et al.
Journal of the American Chemical Society (2016) Vol. 138, Iss. 48, pp. 15629-15635
Closed Access | Times Cited: 148
Stereoselective Solid‐State Synthesis of Substituted Cyclobutanes Assisted by Pseudorotaxane‐like MOFs
Feilong Hu, Yan Mi, Chen Zhu, et al.
Angewandte Chemie International Edition (2018) Vol. 57, Iss. 39, pp. 12696-12701
Open Access | Times Cited: 112
Recent developments in the construction of metallacycle/metallacage-cored supramolecular polymers via hierarchical self-assembly
Bo Li, He Tian, Yiqi Fan, et al.
Chemical Communications (2019) Vol. 55, Iss. 56, pp. 8036-8059
Closed Access | Times Cited: 98
Supramolecularly Catalyzed Polymerization: From Consecutive Dimerization to Polymerization
Xiaoyan Tang, Zehuan Huang, Hao Chen, et al.
Angewandte Chemie International Edition (2018) Vol. 57, Iss. 28, pp. 8545-8549
Closed Access | Times Cited: 89
Cucurbit[7]uril as a Supramolecular Artificial Enzyme for Diels–Alder Reactions
Aniello Palma, Markus Artelsmair, Guanglu Wu, et al.
Angewandte Chemie International Edition (2017) Vol. 56, Iss. 49, pp. 15688-15692
Open Access | Times Cited: 87
Cucurbit[n]urils for Supramolecular Catalysis
Bohan Tang, Jiantao Zhao, Jiang‐Fei Xu, et al.
Chemistry - A European Journal (2020) Vol. 26, Iss. 67, pp. 15446-15460
Closed Access | Times Cited: 77
Supramolecular catalyst functions in catalytic amount: cucurbit[8]uril accelerates the photodimerization of Brooker’s merocyanine
Yuetong Kang, Xiaoyan Tang, Hongde Yu, et al.
Chemical Science (2017) Vol. 8, Iss. 12, pp. 8357-8361
Open Access | Times Cited: 82
Selective Photodimerization in a Cyclodextrin Metal–Organic Framework
Xiao‐Yang Chen, Haoyuan Chen, Luka Đorđević∞, et al.
Journal of the American Chemical Society (2021) Vol. 143, Iss. 24, pp. 9129-9139
Open Access | Times Cited: 48
Cucurbituril-activated photoreaction of dithienylethene for controllable targeted lysosomal imaging and anti-counterfeiting
Guoxing Liu, Xiufang Xu, Xianyin Dai, et al.
Materials Horizons (2021) Vol. 8, Iss. 9, pp. 2494-2502
Closed Access | Times Cited: 44
Supramolecular Catalysis of a Catalysis-Resistant Diels–Alder Reaction: Almost Theoretical Acceleration of Cyclopentadiene Dimerization inside Cucurbit[7]uril
Foad N. Tehrani, Khaleel I. Assaf, Robert Hein, et al.
ACS Catalysis (2022) Vol. 12, Iss. 4, pp. 2261-2269
Closed Access | Times Cited: 31
Chiral Supramolecular U-Shaped Catalysts Induce the Multiselective Diels–Alder Reaction of Propargyl Aldehyde
Manabu Hatano, Tatsuhiro Sakamoto, Tomokazu Mizuno, et al.
Journal of the American Chemical Society (2018) Vol. 140, Iss. 47, pp. 16253-16263
Closed Access | Times Cited: 49
Confinement induced thermodynamic and kinetic facilitation of some Diels–Alder reactions inside a CB[7] cavitand
Debdutta Chakraborty, Pratim Kumar Chattaraj
Journal of Computational Chemistry (2017) Vol. 39, Iss. 3, pp. 151-160
Closed Access | Times Cited: 47
Contrasting pKa Shifts in Cucurbit[7]uril Host–Guest Complexes Governed by an Interplay of Hydrophobic Effects and Electrostatic Interactions
Nuno Basílio, Sandra Gago, A. Jorge Parola, et al.
ACS Omega (2017) Vol. 2, Iss. 1, pp. 70-75
Open Access | Times Cited: 41
Cucurbiturils in supramolecular catalysis
Sebastian Funk, J. Schatz
Journal of Inclusion Phenomena and Macrocyclic Chemistry (2019) Vol. 96, Iss. 1-2, pp. 1-27
Closed Access | Times Cited: 40
Kinetics Inside, Outside and Through Cucurbiturils
Eric Masson, Mersad Raeisi, Kondalarao Kotturi
Israel Journal of Chemistry (2018) Vol. 58, Iss. 3-4, pp. 413-434
Open Access | Times Cited: 39
Applications of macrocyclic compounds for electrochemical sensors to improve selectivity and sensitivity
Huan Luo, Lixia Chen, Qingmei Ge, et al.
Journal of Inclusion Phenomena and Macrocyclic Chemistry (2019) Vol. 95, Iss. 3-4, pp. 171-198
Closed Access | Times Cited: 36
Calix[8]arene nanoreactor for Cu(i)-catalysed C–S coupling
Edmundo G. Percástegui, David J. Hernández, Iván Castillo
Chemical Communications (2015) Vol. 52, Iss. 15, pp. 3111-3114
Closed Access | Times Cited: 37
Cucurbit[7]uril as a Supramolecular Artificial Enzyme for Diels–Alder Reactions
Aniello Palma, Markus Artelsmair, Guanglu Wu, et al.
Angewandte Chemie (2017) Vol. 129, Iss. 49, pp. 15894-15898
Open Access | Times Cited: 36
Investing in entropy: the strategy of cucurbit[n]urils to accelerate the intramolecular Diels–Alder cycloaddition reaction of tertiary furfuryl amines
Karen de la Vega‐Hernández, Marcos G. Suero, Pablo Ballester
Chemical Science (2024) Vol. 15, Iss. 23, pp. 8841-8849
Open Access | Times Cited: 3
Rigid Organization of Fluorescence-Active Ligands by Artificial Macrocyclic Receptor to Achieve the Thioflavin T-Amyloid Fibril Level Association
Ying‐Ming Zhang, Xu‐Jie Zhang, Xiufang Xu, et al.
The Journal of Physical Chemistry B (2016) Vol. 120, Iss. 16, pp. 3932-3940
Closed Access | Times Cited: 30
A Pyrene‐Linked Cavity within a β‐Barrel Protein Promotes an Asymmetric Diels–Alder Reaction
Tomoki Himiyama, Naomasa Taniguchi, Shunsuke Kato, et al.
Angewandte Chemie International Edition (2017) Vol. 56, Iss. 44, pp. 13618-13622
Closed Access | Times Cited: 30
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