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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:

Stereochemical diversity in pyrrolidine synthesis by catalytic asymmetric 1,3-dipolar cycloaddition of azomethine ylides
Javier Adrio, Juan C. Carretero
Chemical Communications (2019) Vol. 55, Iss. 80, pp. 11979-11991
Open Access | Times Cited: 133

Showing 26-50 of 133 citing articles:

Atroposelective Synthesis of Axially Chiral Naphthylpyrroles by a Catalytic Asymmetric 1,3-Dipolar Cycloaddition/Aromatization Sequence
Ian Maclean, Enrique Gallent, Oscar Orozco, et al.
Organic Letters (2024) Vol. 26, Iss. 4, pp. 922-927
Open Access | Times Cited: 5
Unveiling the high regioselectivity and stereoselectivity within the synthesis of spirooxindolenitropyrrolidine: A molecular electron density theory perspective
Nivedita Acharjee, Haydar Mohammad-Salim, Mrinmoy Chakraborty, et al.
Journal of Physical Organic Chemistry (2021) Vol. 34, Iss. 6
Closed Access | Times Cited: 31
NHC-catalysed retro-aldol/aldol cascade reaction enabling solvent-controlled stereodivergent synthesis of spirooxindoles
Hai‐Jun Leng, Qian Zhao, Qing Mao, et al.
Chinese Chemical Letters (2021) Vol. 32, Iss. 8, pp. 2567-2571
Closed Access | Times Cited: 31
Combination of Pseudo‐Natural Product Design and Formal Natural Product Ring Distortion Yields Stereochemically and Biologically Diverse Pseudo‐Sesquiterpenoid Alkaloids
Jie Liu, Jana Flegel, Felix Otte, et al.
Angewandte Chemie International Edition (2021) Vol. 60, Iss. 39, pp. 21384-21395
Open Access | Times Cited: 31
Reactivity and Selectivity of the Diels–Alder Reaction of Anthracene in [Pd6L4]12+ Supramolecular Cages: A Computational Study
Xin‐Rui Mao, Qian Wang, Shuping Zhuo, et al.
Inorganic Chemistry (2023) Vol. 62, Iss. 10, pp. 4330-4340
Closed Access | Times Cited: 12
Asymmetric Relay Catalysis Enables Unreactive Allylic Alcohols to Participate in 1,3-Dipolar Cycloaddition of Azomethine Ylides
Xiang Cheng, Cong Fu, Bobin Chen, et al.
Journal of the American Chemical Society (2025)
Closed Access
Reflexive Chirality Transfer (RCT): Asymmetric 1,3-Dipolar Cycloaddition of α-Amino Acid Schiff Base with Nonchiral Copper Catalyst
Kazuhiro Morisaki, Yuto Furuki, Rento Kousaka, et al.
Journal of the American Chemical Society (2025)
Closed Access
Recent Developments in Enantioselective Silver-Catalyzed Transformations
Hélène Pellissier
Organic Preparations and Procedures International (2025), pp. 1-95
Closed Access
Asymmetric Cross [10+2] Cycloadditions of 2‐Alkylidene‐1‐indanones and Activated Alkenes under Phase‐Transfer Catalysis
Yang Yang, Ying Jiang, Wei Du, et al.
Chemistry - A European Journal (2019) Vol. 26, Iss. 8, pp. 1754-1758
Closed Access | Times Cited: 31
N-tert-Butanesulfinyl imines in the asymmetric synthesis of nitrogen-containing heterocycles
Joseane A. Mendes, Paulo R. R. Costa, Miguel Yus, et al.
Beilstein Journal of Organic Chemistry (2021) Vol. 17, pp. 1096-1140
Open Access | Times Cited: 24
Catalytic asymmetric synthesis of enantioenriched α-deuterated pyrrolidine derivatives
Xin Chang, Xiang Cheng, Chun‐Jiang Wang
Chemical Science (2022) Vol. 13, Iss. 14, pp. 4041-4049
Open Access | Times Cited: 17
Silver-Mediated [3 + 2] Cycloaddition of Azomethine Ylides with Trifluoroacetimidoyl Chlorides for the Synthesis of 5-(Trifluoromethyl)imidazoles
Hefei Yang, Shu‐Ning Lu, Zhengkai Chen, et al.
The Journal of Organic Chemistry (2021) Vol. 86, Iss. 5, pp. 4361-4370
Closed Access | Times Cited: 23
Copper-catalyzed [3 + 2]-cycloaddition of α-halonitroalkenes with azomethine ylides: facile synthesis of multisubstituted pyrrolidines and pyrroles
Vladimir Motornov, Andrey A. Tabolin, Yulia V. Nelyubina, et al.
Organic & Biomolecular Chemistry (2021) Vol. 19, Iss. 15, pp. 3413-3427
Closed Access | Times Cited: 23
Pyrrolidine Derivatives as Anti‐diabetic Agents: Current Status and Future Prospects
Aeyaz Ahmad Bhat, Nitin Tandon, Runjhun Tandon
ChemistrySelect (2022) Vol. 7, Iss. 6
Closed Access | Times Cited: 16
Higher-order [10 + 2] cycloaddition of 2-alkylidene-1-indanones enables the dearomatization of 3-nitroindoles: access to polycyclic cyclopenta[b]indoline derivatives
Jian‐Qiang Zhao, Zhou Shun, Hui-Ling Qian, et al.
Organic Chemistry Frontiers (2022) Vol. 9, Iss. 12, pp. 3322-3327
Closed Access | Times Cited: 15
Organocatalytic Enantioselective 1,3‐Dipolar [6+4] Cycloadditions of Tropone
Giulio Bertuzzi, David McLeod, Lisa‐Marie Mohr, et al.
Chemistry - A European Journal (2020) Vol. 26, Iss. 67, pp. 15491-15496
Closed Access | Times Cited: 22
Stereodivergent Synthesis of Enantioenriched γ‐Butyrolactones Bearing Two Vicinal Stereocenters Enabled by Synergistic Copper and Iridium Catalysis
Lu Xiao, Liang Wei, Chun‐Jiang Wang
Angewandte Chemie (2021) Vol. 133, Iss. 47, pp. 25134-25144
Closed Access | Times Cited: 20
Copper-Catalyzed Asymmetric 1,3-Dipolar Cycloaddition of Imino Esters to Unsaturated Sultones
Shohei Furuya, Kazuya Kanemoto, Shin‐ichi Fukuzawa
The Journal of Organic Chemistry (2020) Vol. 85, Iss. 12, pp. 8142-8148
Closed Access | Times Cited: 20
Cu-catalyzed endo-selective asymmetric 1,3-dipolar cycloaddition of azomethine ylides with ethenesulfonyl fluorides: Efficient access to chiral pyrrolidine-3-sulfonyl fluorides
Yinan Li, Xin Chang, Qi Xiong, et al.
Chinese Chemical Letters (2021) Vol. 32, Iss. 12, pp. 4029-4032
Closed Access | Times Cited: 17
Enhancing the Efficacy of Chiral Ligands and Catalysts: Siloxane-Substituted Oxazoline Ferrocenes as Next-Generation Candidates
Li Dai, Zhao Li, Di Xu, et al.
Molecules (2024) Vol. 29, Iss. 5, pp. 968-968
Open Access | Times Cited: 2
Peptide Macrocyclization via Cu-catalyzed 1,3-Dipolar Cycloaddition of Azomethine Ylides
Javier Adrio, Nuria Rodríguez, Juan C. Carretero, et al.
(2024)
Open Access | Times Cited: 2
Predicting Absolute Rate Constants for Huisgen Reactions of Unsaturated Iminium Ions with Diazoalkanes
Jingjing Zhang, Quan Chen, Robert J. Mayer, et al.
Angewandte Chemie International Edition (2020) Vol. 59, Iss. 30, pp. 12527-12533
Open Access | Times Cited: 17
Chiral Trifluoromethylated Pyrrolidines via Cu–Catalyzed Asymmetric 1,3‐Dipolar Cycloaddition
Xiang Cheng, Dingce Yan, Xiu‐Qin Dong, et al.
Asian Journal of Organic Chemistry (2020) Vol. 9, Iss. 10, pp. 1567-1570
Closed Access | Times Cited: 17
Catalytic Enantioselective Formal Synthesis of MDM2 Antagonist RG7388 and Its Analogues
Xuejie Zou, Wu‐Lin Yang, Jing‐Yan Zhu, et al.
Chinese Journal of Chemistry (2020) Vol. 38, Iss. 5, pp. 435-438
Closed Access | Times Cited: 16
Synthesis of bioactive fluoropyrrolidinesviacopper(i)-catalysed asymmetric 1,3-dipolar cycloaddition of azomethine ylides
Xiao Li Xu, Longzhu Bao, Ran Lu, et al.
Chemical Science (2021) Vol. 13, Iss. 5, pp. 1398-1407
Open Access | Times Cited: 15

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