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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:

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

Showing 1-25 of 56 citing articles:

Exploiting Heavier Organochalcogen Compounds in Donor–Acceptor Cyclopropane Chemistry
André U. Augustin, Daniel B. Werz
Accounts of Chemical Research (2021) Vol. 54, Iss. 6, pp. 1528-1541
Closed Access | Times Cited: 130
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: 85
Hexafluoroisopropanol Promoted Ring‐Opening‐Cyclization of Donor–Acceptor Cyclopropanes with Primary Amines
Srinivasarao Yaragorla, Rajeshwari Tangellapally, Doma Arun
European Journal of Organic Chemistry (2024) Vol. 27, Iss. 22
Closed Access | Times Cited: 9
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
Friedel–Crafts-Type Reactions with Electrochemically Generated Electrophiles from Donor–Acceptor Cyclopropanes and -Butanes
Simon Kolb, Nils L. Ahlburg, Daniel B. Werz
Organic Letters (2021) Vol. 23, Iss. 14, pp. 5549-5553
Closed Access | Times Cited: 45
Copper-Catalyzed Ring-Opening 1,3-Aminotrifluoromethylation of Arylcyclopropanes
Huan Zhang, Haiwen Xiao, Feng Jiang, et al.
Organic Letters (2021) Vol. 23, Iss. 6, pp. 2268-2272
Closed Access | Times Cited: 33
cis-Selective, Enantiospecific Addition of Donor–Acceptor Cyclopropanes to Activated Alkenes: An Iodination/Michael-Cyclization Cascade
Nils L. Ahlburg, Peter G. Jones, Daniel B. Werz
Organic Letters (2020) Vol. 22, Iss. 16, pp. 6404-6408
Closed 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
Multicomponent, Tandem 1,3- and 1,4-Bisarylation of Donor–Acceptor Cyclopropanes and Cyclobutanes with Electron-Rich Arenes and Hypervalent Arylbismuth Reagents
Biplab Mondal, Dinabandhu Das, Jaideep Saha
Organic Letters (2020) Vol. 22, Iss. 13, pp. 5115-5120
Closed Access | Times Cited: 33
Electricity Driven 1,3‐Oxohydroxylation of Donor‐Acceptor Cyclopropanes: a Mild and Straightforward Access to β‐Hydroxy Ketones
Debarshi Saha, Irshad Maajid Taily, Prabal Banerjee
European Journal of Organic Chemistry (2021) Vol. 2021, Iss. 36, pp. 5053-5057
Closed Access | Times Cited: 30
Insertion of S2 into Donor–Acceptor Cyclopropanes: Access to Dithiolanes and Their Conversion to Thietane Dioxides
Anu Jacob, Philip Barkawitz, Peter G. Jones, et al.
Organic Letters (2022) Vol. 24, Iss. 16, pp. 3028-3032
Closed Access | Times Cited: 20
Benzotriazole-Triggered Three-Component Lewis Acid-Catalyzed Ring-Opening 1,3-Aminofunctionalization of Donor–Acceptor Cyclopropanes
Shiksha Deswal, Avishek Guin, Akkattu T. Biju
Organic Letters (2023) Vol. 25, Iss. 10, pp. 1643-1648
Closed Access | Times Cited: 12
Ring-Opening 1,3-Sulfonylation-Fluorination of Donor–Acceptor Cyclopropanes: Three-Component Access to γ-Fluorosulfones
Gwyndaf A. Oliver, Daniel B. Werz
Organic Letters (2023) Vol. 25, Iss. 19, pp. 3568-3572
Closed Access | Times Cited: 12
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
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
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 (2021) Vol. 133, Iss. 29, pp. 16064-16070
Open Access | Times Cited: 25
Ring-Opening 1,3-Carbothiolation of Donor–Acceptor Cyclopropanes Using Alkyl Halides and In Situ Generated Dithiocarbamates
Avishek Guin, Shiksha Deswal, Akkattu T. Biju
The Journal of Organic Chemistry (2022) Vol. 87, Iss. 9, pp. 6504-6513
Closed Access | Times Cited: 18
Photoinduced rapid Chloropropylation of Quinoxalin-2(1H)-ones with Cyclopropane and HCl
Chenfeng Liang, Zhihao Wang, Qing Chen, et al.
Molecular Catalysis (2024) Vol. 558, pp. 114024-114024
Closed Access | Times Cited: 3
GaCl3-Mediated Cascade [2 + 4]-Cycloaddition/[4 + 2]-Annulation of Donor–Acceptor Cyclopropanes with Conjugated Dienes: Strategy for the Construction of Benzobicyclo[3.3.1]nonane Skeleton
Maria A. Zotova, Daniil A. Knyazev, Denis D. Borisov, et al.
The Journal of Organic Chemistry (2021) Vol. 86, Iss. 12, pp. 8089-8100
Closed Access | Times Cited: 21
Functionalization of Sydnones with Donor‐Acceptor Cyclopropanes, Cyclobutanes, and Michael Acceptors
Nils L. Ahlburg, Tyll Freese, Simon Kolb, et al.
European Journal of Organic Chemistry (2021) Vol. 2021, Iss. 10, pp. 1603-1606
Open Access | Times Cited: 18
Metal-Free Regioselective Hydrophosphorodithioation of Spirovinylcyclopropyl Oxindoles: Rapid Access to Allyl Dialkylphosphorodithioates
Jiahua Wang, Fang Han, Siyuan Hao, et al.
The Journal of Organic Chemistry (2022) Vol. 87, Iss. 19, pp. 12844-12853
Closed Access | Times Cited: 13
Lewis acid catalysed asymmetric cascade reaction of cyclopropyl ketones: concise synthesis of pyrrolobenzothiazoles
Fenzhen Chang, Bin Shen, Sijing Wang, et al.
Chemical Communications (2020) Vol. 56, Iss. 87, pp. 13429-13432
Closed Access | Times Cited: 20
Lewis acid-catalyzed one-pot thioalkenylation of donor–acceptor cyclopropanes using in situ generated dithiocarbamates and propiolates
Sanjeevni Harikumar, Labeeb Thazhe Kollorth Kandy, Avishek Guin, et al.
Organic & Biomolecular Chemistry (2024) Vol. 22, Iss. 9, pp. 1834-1838
Closed Access | Times Cited: 2
LiBr-Catalyzed C3-Disulfuration between Indole and N-Dithiophthalimide
Dungai Wang, Wangyu Li, Keqiang Shi, et al.
The Journal of Organic Chemistry (2022) Vol. 88, Iss. 4, pp. 2550-2556
Closed Access | Times Cited: 11
The Cloke–Wilson rearrangement of aroyl-substituted donor–acceptor cylopropanes containing arylethyl donors
Subaramaniam Thangamalar, Murugesan Thangamani, Kannupal Srinivasan
Organic & Biomolecular Chemistry (2022) Vol. 20, Iss. 15, pp. 3145-3153
Closed Access | Times Cited: 11
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