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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:

Ringöffnende 1‐Amino‐3‐aminomethylierung von Donor‐Akzeptor‐substituierten Cyclopropanen über 1,3‐Diazepane
Lennart K. B. Garve, Peter G. Jones, Daniel B. Werz
Angewandte Chemie (2017) Vol. 129, Iss. 31, pp. 9354-9358
Closed Access | Times Cited: 41

Showing 1-25 of 41 citing articles:

Donor–Acceptor Cyclopropanes as an Expedient Building Block Towards the Construction of Nitrogen‐Containing Molecules: An Update
Priyanka Singh, Rohit Kumar Varshnaya, Raghunath Dey, et al.
Advanced Synthesis & Catalysis (2019) Vol. 362, Iss. 7, pp. 1447-1484
Closed Access | Times Cited: 144
Kinetic Studies of Donor–Acceptor Cyclopropanes: The Influence of Structural and Electronic Properties on the Reactivity
Alexander Kreft, Alexander Lücht, Jörg Grunenberg, et al.
Angewandte Chemie International Edition (2018) Vol. 58, Iss. 7, pp. 1955-1959
Open Access | Times Cited: 119
(3+3)‐Annulation of Donor–Acceptor Cyclopropanes with Diaziridines
Alexey O. Chagarovskiy, Vladimir S. Vasin, Vladimir V. Kuznetsov, et al.
Angewandte Chemie International Edition (2018) Vol. 57, Iss. 32, pp. 10338-10342
Closed Access | Times Cited: 118
Stereospecific Reactions of Donor–Acceptor Cyclopropanes with Thioketones: Access to Highly Substituted Tetrahydrothiophenes
André U. Augustin, Maximilian Sensse, Peter G. Jones, et al.
Angewandte Chemie International Edition (2017) Vol. 56, Iss. 45, pp. 14293-14296
Open Access | Times Cited: 116
Stereospecific 1,3‐Aminobromination of Donor–Acceptor Cyclopropanes
Saikat Das, Constantin G. Daniliuc, Armido Studer
Angewandte Chemie International Edition (2017) Vol. 56, Iss. 38, pp. 11554-11558
Closed Access | Times Cited: 112
Lewis Acid Catalyzed Stereoselective Dearomative Coupling of Indolylboron Ate Complexes with Donor–Acceptor Cyclopropanes and Alkyl Halides
Saikat Das, Constantin G. Daniliuc, Armido Studer
Angewandte Chemie International Edition (2018) Vol. 57, Iss. 15, pp. 4053-4057
Closed Access | Times Cited: 111
(3+3)‐Annulation of Carbonyl Ylides with Donor–Acceptor Cyclopropanes: Synergistic Dirhodium(II) and Lewis Acid Catalysis
Martin Petzold, Peter G. Jones, Daniel B. Werz
Angewandte Chemie International Edition (2019) Vol. 58, Iss. 19, pp. 6225-6229
Open Access | Times Cited: 101
Reactions of Donor–Acceptor Cyclopropanes with Naphthoquinones: Redox and Lewis Acid Catalysis Working in Concert
Alexander Lücht, Lukas J. Patalag, André U. Augustin, et al.
Angewandte Chemie International Edition (2017) Vol. 56, Iss. 35, pp. 10587-10591
Open Access | Times Cited: 84
Ring‐Opening 1,3‐Aminochalcogenation of Donor–Acceptor Cyclopropanes: A Three‐Component Approach
André U. Augustin, Peter G. Jones, Daniel B. Werz
Chemistry - A European Journal (2019) Vol. 25, Iss. 50, pp. 11620-11624
Open Access | Times Cited: 62
Electroreductive Cross‐Electrophile Coupling of Aziridines and Aryl Bromides
Guoqing Yang, Yanwei Wang, Youai Qiu
Chemistry - A European Journal (2023) Vol. 29, Iss. 36
Closed Access | Times Cited: 18
Three‐Component Gallium(III)‐Promoted Addition of Halide Anions and Acetylenes to Donor–Acceptor Cyclopropanes
Роман А. Новиков, Denis D. Borisov, Anna V. Tarasova, et al.
Angewandte Chemie International Edition (2018) Vol. 57, Iss. 32, pp. 10293-10298
Closed Access | Times Cited: 52
Lewis Base‐Promoted Ring‐Opening 1,3‐Dioxygenation of Unactivated Cyclopropanes Using a Hypervalent Iodine Reagent
Matthew H. Gieuw, Zhihai Ke, Ying‐Yeung Yeung
Angewandte Chemie International Edition (2018) Vol. 57, Iss. 14, pp. 3782-3786
Closed Access | Times Cited: 48
Inverse‐Electron‐Demand [4+2]‐Cycloaddition of 1,3,5‐triazinanes: Facile Approaches to Tetrahydroquinazolines
Yongsheng Zheng, Liangcheng Tu, Na Li, et al.
Advanced Synthesis & Catalysis (2018) Vol. 361, Iss. 1, pp. 44-48
Closed Access | Times Cited: 47
Regio‐ and Stereoselective Synthesis of Functionalized Dihydropyridines, Pyridines, and 2H‐Pyrans: Heck Coupling of Monocyclopropanated Heterocycles
Julietta Yedoyan, Nikolai Wurzer, Urszula Klimczak, et al.
Angewandte Chemie International Edition (2019) Vol. 58, Iss. 11, pp. 3594-3598
Closed Access | Times Cited: 41
Stereospecific 1,3‐Aminobromination of Donor–Acceptor Cyclopropanes
Saikat Das, Constantin G. Daniliuc, Armido Studer
Angewandte Chemie (2017) Vol. 129, Iss. 38, pp. 11712-11716
Closed Access | Times Cited: 41
Lewis Acid Catalyzed Stereoselective Dearomative Coupling of Indolylboron Ate Complexes with Donor–Acceptor Cyclopropanes and Alkyl Halides
Saikat Das, Constantin G. Daniliuc, Armido Studer
Angewandte Chemie (2018) Vol. 130, Iss. 15, pp. 4117-4121
Closed Access | Times Cited: 38
Stereospezifische Reaktion von Donor‐Akzeptor‐Cyclopropanen mit Thioketonen: ein Zugang zu hoch substituierten Tetrahydrothiophenen
André U. Augustin, Maximilian Sensse, Peter G. Jones, et al.
Angewandte Chemie (2017) Vol. 129, Iss. 45, pp. 14481-14485
Closed Access | Times Cited: 35
Synthesis of Indenopyridine Derivatives via MgI2‐Promoted [2+4] Cycloaddition Reaction of In‐situ Generated 2‐Styrylmalonate from Donor‐Acceptor Cyclopropanes and Chalconimines
Kamal Verma, Prabal Banerjee
Advanced Synthesis & Catalysis (2018) Vol. 360, Iss. 19, pp. 3687-3692
Closed Access | Times Cited: 33
(3+3)‐Annulation of Donor–Acceptor Cyclopropanes with Diaziridines
Alexey O. Chagarovskiy, Vladimir S. Vasin, Vladimir V. Kuznetsov, et al.
Angewandte Chemie (2018) Vol. 130, Iss. 32, pp. 10495-10499
Closed Access | Times Cited: 33
New Dyes Based on Extended Fulvene Motifs: Synthesis through Redox Reactions of Naphthoquinones with Donor–Acceptor Cyclopropanes and Their Spectroelectrochemical Behavior
Alexander Lücht, Sebastian Sobottka, Lukas J. Patalag, et al.
Chemistry - A European Journal (2019) Vol. 25, Iss. 44, pp. 10359-10365
Open Access | Times Cited: 32
(3+3)‐Annulation of Carbonyl Ylides with Donor–Acceptor Cyclopropanes: Synergistic Dirhodium(II) and Lewis Acid Catalysis
Martin Petzold, Peter G. Jones, Daniel B. Werz
Angewandte Chemie (2019) Vol. 131, Iss. 19, pp. 6291-6295
Open Access | Times Cited: 30
Kinetische Studie zu Donor‐Akzeptor‐Cyclopropanen: Strukturelle und elektronische Einflüsse auf die Reaktivität
Alexander Lücht, Alexander Kreft, Jörg Grunenberg, et al.
Angewandte Chemie (2018) Vol. 131, Iss. 7, pp. 1975-1979
Closed Access | Times Cited: 30
Chiral N,N′‐Dioxide/ScΙΙΙ Complex‐Catalyzed Asymmetric Ring‐Opening Reaction of Cyclopropyl Ketones with Indoles
Fenzhen Chang, Lili Lin, Yong Xia, et al.
Advanced Synthesis & Catalysis (2018) Vol. 360, Iss. 14, pp. 2608-2612
Closed Access | Times Cited: 29
Reaktionen von Donor‐Akzeptor‐Cyclopropanen mit Naphthochinonen: eine Kombination aus Redox‐ und Lewis‐Säure‐Katalyse
Alexander Lücht, Lukas J. Patalag, André U. Augustin, et al.
Angewandte Chemie (2017) Vol. 129, Iss. 35, pp. 10723-10727
Closed Access | Times Cited: 26
Carboxylates as Nucleophiles in the Enantioselective Ring‐Opening of Formylcyclopropanes under Iminium Ion Catalysis
Estíbaliz Díaz, Efraím Reyes, Uxue Uria, et al.
Chemistry - A European Journal (2018) Vol. 24, Iss. 35, pp. 8764-8768
Open Access | Times Cited: 22
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