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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 AgOAc/quinine-derived aminophosphine complex as an efficient catalyst for diastereo- and enantioselective 1,3-dipolar cycloaddition of α,β-unsaturated 7-azaindoline amides and azomethine ylides
Yanping Zhang, Yong You, Jian‐Qiang Zhao, et al.
Organic Chemistry Frontiers (2019) Vol. 6, Iss. 11, pp. 1879-1884
Closed Access | Times Cited: 11

Showing 11 citing articles:

Stereodivergent synthesis of enantioenriched azepino[3,4,5-cd]-indoles via cooperative Cu/Ir-catalyzed asymmetric allylic alkylation and intramolecular Friedel–Crafts reaction
Lu Xiao, Bo Li, Fan Xiao, et al.
Chemical Science (2022) Vol. 13, Iss. 17, pp. 4801-4812
Open Access | Times Cited: 43
β-Substituted Alkenyl Heteroarenes as Dipolarophiles in the Cu(I)-Catalyzed Asymmetric 1,3-Dipolar Cycloaddition of Azomethine Ylides Empowered by a Dual Activation Strategy: Stereoselectivity and Mechanistic Insight
Xin Chang, Yuhong Yang, Chong Shen, et al.
Journal of the American Chemical Society (2021) Vol. 143, Iss. 9, pp. 3519-3535
Closed Access | Times Cited: 44
Azaindole therapeutic agents
Damoder Reddy Motati, Radhika Amaradhi, Thota Ganesh
Bioorganic & Medicinal Chemistry (2020) Vol. 28, Iss. 24, pp. 115830-115830
Open Access | Times Cited: 36
Recent developments in the synthesis of azaindoles from pyridine and pyrrole building blocks
Damoder Reddy Motati, Radhika Amaradhi, Thota Ganesh
Organic Chemistry Frontiers (2020) Vol. 8, Iss. 3, pp. 466-513
Closed Access | Times Cited: 36
Organocatalytic asymmetric [3+2]-cycloaddition of 3-isothiocyanato oxindoles with 1,3,5-trisubstituted-hexahydro-1,3,5-triazines to access spiro-imidazolidinethione-oxindoles
Chuanbao Zhang, Pei‐Hao Dou, Yong You, et al.
Tetrahedron (2019) Vol. 75, Iss. 40, pp. 130571-130571
Closed Access | Times Cited: 24
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
Catalytic asymmetric synthesis of diazabicyclo[3.1.0]hexanes by 1,3-dipolar cycloaddition of azomethine ylides with azirines
Alba Molina, Sergio Díaz‐Tendero, Javier Adrio, et al.
Chemical Communications (2020) Vol. 56, Iss. 37, pp. 5050-5053
Open Access | Times Cited: 12
Metal‐Catalyst‐Free One‐Pot Aqueous Synthesis of trans‐1,2‐Diols from Electron‐Deficient α,β‐Unsaturated Amides via Epoxidation Using Oxone as a Dual Role Reagent
Ming‐Zhong Zhang, Ping Wang, Haiyan Liu, et al.
ChemSusChem (2023) Vol. 16, Iss. 18
Closed Access | Times Cited: 3
(2R,3S)‐3,4,4,4‐Tetrafluorovaline: A Fluorinated Bioisostere of Isoleucine
Lennart Brewitz, Hidetoshi Noda, Naoya Kumagai, et al.
European Journal of Organic Chemistry (2020) Vol. 2020, Iss. 11, pp. 1745-1752
Open Access | Times Cited: 7
Progress in Catalytic Asymmetric Reactions with 7-Azaindoline as the Directing Group
Yanping Zhang, Yong You, Jun‐Qing Yin, et al.
Molecules (2023) Vol. 28, Iss. 23, pp. 7898-7898
Open Access | Times Cited: 1
Well-defined Cu(I) complexes based on [N,P]-pyrrole ligands catalyzed a highly endo-selective 1,3-dipolar cycloaddition
Miguel A. Alvarado-Castillo, Salvador Cortés‐Mendoza, José E. Barquera‐Lozada, et al.
Dalton Transactions (2023) Vol. 53, Iss. 5, pp. 2231-2241
Open Access
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