Open Access Helper

OpenAlex Citation Counts

OpenAlex Citations Logo

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:

Directing the Activation of Donor–Acceptor Cyclopropanes Towards Stereoselective 1,3‐Dipolar Cycloaddition Reactions by Brønsted Base Catalysis
Jakob Blom, Andreu Vidal‐Albalat, Julie Jørgensen, et al.
Angewandte Chemie International Edition (2017) Vol. 56, Iss. 39, pp. 11831-11835
Closed Access | Times Cited: 66

Showing 1-25 of 66 citing articles:

Catalytic Enantioselective Ring-Opening Reactions of Cyclopropanes
Vincent Pirenne, Bastian Muriel, Jérôme Waser
Chemical Reviews (2020) Vol. 121, Iss. 1, pp. 227-263
Open Access | Times Cited: 408
Highly enantioselective carbene insertion into N–H bonds of aliphatic amines
Mao‐Lin Li, Jinhan Yu, Yi-Hao Li, et al.
Science (2019) Vol. 366, Iss. 6468, pp. 990-994
Open Access | Times Cited: 246
Asymmetric Catalytic Reactions of Donor–Acceptor Cyclopropanes
Yong Xia, Xiaohua Liu, Xiaoming Feng
Angewandte Chemie International Edition (2020) Vol. 60, Iss. 17, pp. 9192-9204
Closed Access | Times Cited: 170
Recent advances in ring-opening of donor acceptor cyclopropanes using C-nucleophiles
Koena Ghosh, Subhomoy Das
Organic & Biomolecular Chemistry (2021) Vol. 19, Iss. 5, pp. 965-982
Closed Access | Times Cited: 107
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
The Cyclopropyl Group as a Neglected Donor in Donor–Acceptor Cyclopropane Chemistry
Alexander Kreft, Peter G. Jones, Daniel B. Werz
Organic Letters (2018) Vol. 20, Iss. 7, pp. 2059-2062
Closed Access | Times Cited: 94
Enantioselective cyanation via radical-mediated C–C single bond cleavage for synthesis of chiral dinitriles
Tao Wang, Yining Wang, Rui Wang, et al.
Nature Communications (2019) Vol. 10, Iss. 1
Open Access | Times Cited: 93
(4 + 3)-Cycloaddition of Donor–Acceptor Cyclopropanes with Thiochalcones: A Diastereoselective Access to Tetrahydrothiepines
André U. Augustin, J. L. Merz, Peter G. Jones, et al.
Organic Letters (2019) Vol. 21, Iss. 23, pp. 9405-9409
Open Access | Times Cited: 84
Electrocatalytic Activation of Donor–Acceptor Cyclopropanes and Cyclobutanes: An Alternative C(sp3)−C(sp3) Cleavage Mode
Simon Kolb, Martin Petzold, Felix Brandt, et al.
Angewandte Chemie International Edition (2021) Vol. 60, Iss. 29, pp. 15928-15934
Open Access | Times Cited: 84
Lewis Acid Catalyzed Ring-Opening 1,3-Aminothiolation of Donor–Acceptor Cyclopropanes Using Sulfenamides
Avishek Guin, Thukaram Rathod, Rahul N. Gaykar, et al.
Organic Letters (2020) Vol. 22, Iss. 6, pp. 2276-2280
Open Access | Times Cited: 56
Pot and time economies in the total synthesis of Corey lactone
Nariyoshi Umekubo, Yurina Suga, Yujiro Hayashi
Chemical Science (2019) Vol. 11, Iss. 5, pp. 1205-1209
Open Access | Times Cited: 55
Cycloadditions of Donor–Acceptor Cyclopropanes and ‐butanes using S=N‐Containing Reagents: Access to Cyclic Sulfinamides, Sulfonamides, and Sulfinamidines
Gwyndaf A. Oliver, Maximilian N. Loch, André U. Augustin, et al.
Angewandte Chemie International Edition (2021) Vol. 60, Iss. 49, pp. 25825-25831
Open Access | Times Cited: 54
The extraordinary gravity of three atom 4π-components and 1,3-dienes to C20-nXn fullerenes; a new gate to the future of Nano technology
Seyyed Amir Siadati, Solmaz Rezazadeh
Scientiae Radices (2022) Vol. 1, Iss. 1, pp. 46-68
Open Access | Times Cited: 34
A novel type of donor–acceptor cyclopropane with fluorine as the donor: (3 + 2)-cycloadditions with carbonyls
Haidong Liu, Lifang Tian, Hui Wang, et al.
Chemical Science (2022) Vol. 13, Iss. 9, pp. 2686-2691
Open Access | Times Cited: 32
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
Enantioselective (8+3) Cycloadditions by Activation of Donor–Acceptor Cyclopropanes Employing Chiral Brønsted Base Catalysis
David McLeod, Mathias Kirk Thøgersen, Casper L. Barløse, et al.
Angewandte Chemie International Edition (2022) Vol. 61, Iss. 29
Open Access | Times Cited: 26
FeCl3-Promoted [3 + 2] Annulations of γ-Butyrolactone Fused Cyclopropanes with Heterocumulenes
Manli Feng, Pengfei Yang, Gaosheng Yang, et al.
The Journal of Organic Chemistry (2017) Vol. 83, Iss. 1, pp. 174-184
Closed Access | Times Cited: 43
Connecting and Analyzing Enantioselective Bifunctional Hydrogen Bond Donor Catalysis Using Data Science Tools
Jacob Werth, Matthew S. Sigman
Journal of the American Chemical Society (2020) Vol. 142, Iss. 38, pp. 16382-16391
Open Access | Times Cited: 38
(3 + 2)-Cycloaddition of Donor–Acceptor Cyclopropanes with Selenocyanate: Synthesis of Dihydroselenophenes and Selenophenes
Anu Jacob, Peter G. Jones, Daniel B. Werz
Organic Letters (2020) Vol. 22, Iss. 21, pp. 8720-8724
Closed Access | Times Cited: 37
Asymmetric Catalytic Reactions of Donor–Acceptor Cyclopropanes
Yong Xia, Xiaohua Liu, Xiaoming Feng
Angewandte Chemie (2020) Vol. 133, Iss. 17, pp. 9276-9288
Closed Access | Times Cited: 33
Cycloaddition and Annulation Reactions of Donor–Acceptor Cyclopropanes
Роман А. Новиков, Denis D. Borisov, Yury V. Tomilov
(2024), pp. 37-138
Closed Access | Times Cited: 4
Asymmetric [3 + 2] cycloaddition of donor–acceptor cyclopropanes with azadienes enabled by Brønsted base catalysis
Shu Li, Zhi-Hong Dong, Si-Yu Dan, et al.
Organic Chemistry Frontiers (2024) Vol. 11, Iss. 10, pp. 2905-2910
Closed Access | Times Cited: 4
Enantioselective (3+2) Annulation of Donor‐Acceptor Cyclopropanes with Aldehydes and Ketones Catalyzed by Brønsted Bases
Erlaitz Basabe Obregón, Louise G. Rost, Ida R. Kocemba, et al.
Angewandte Chemie International Edition (2024)
Closed Access | Times Cited: 4
Ring-Opening Reactions of Donor–Acceptor Cyclopropanes with Some Enolizable Azaheterocyclic Thiones: S- versus N-Attack
Grzegorz Mlostoń, Mateusz Kowalczyk, Małgorzata Celeda, et al.
Synlett (2025)
Closed Access
Enantioselective Formation of Isoxazolidines via Brønsted-Base Catalyzed (3 + 2) Annulation of Cyclopropanes with Nitrosoarenes
Erlaitz Basabe Obregón, Leire Villaescusa, José Trujillo‐Sierra, et al.
Journal of the American Chemical Society (2025)
Closed Access
Page 1 - Next Page

Scroll to top