OpenAlex Citation Counts

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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:

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

Showing 26-50 of 62 citing articles:

K2CO3‐Promoted Ring‐Opening/Cyclization Reactions of Multi‐substituted Donor‐Acceptor Cyclopropanes with Thiourea: Access to 2‐Amino‐4,6‐diarylnicotinonitrile Derivatives
Shan Wang, Zengyang Xie, Mingshuang Li, et al.
ChemistrySelect (2020) Vol. 5, Iss. 20, pp. 6011-6015
Closed Access | Times Cited: 15

Ring Opening of Donor–Acceptor Cyclopropanes with Acyclic 1,3-Diketones for the Synthesis of 1,6-Dicarbonyl Compounds
Dongxin Zhang, Hu Cai, Yan Chen, et al.
The Journal of Organic Chemistry (2020) Vol. 85, Iss. 21, pp. 14262-14270
Closed Access | Times Cited: 15

DBU-promoted ring-opening reactions of multi-substituted donor–acceptor cyclopropanes: access to functionalized chalcones with a quaternary carbon group
Naili Luo, Jiamin Liu, Shan Wang, et al.
Organic & Biomolecular Chemistry (2020) Vol. 18, Iss. 45, pp. 9210-9215
Closed Access | Times Cited: 15

Reactions of Styrylmalonates with Aromatic Aldehydes: Detailed Synthetic and Mechanistic Studies
Denis D. Borisov, Роман А. Новиков, Yury V. Tomilov
The Journal of Organic Chemistry (2021) Vol. 86, Iss. 6, pp. 4457-4471
Closed Access | Times Cited: 13

A Widely Applicable and Versatile Method for the Ring‐Opening 1,3‐Carbocarbonation of Donor‐Acceptor Cyclopropanes
Heinrich F. von Köller, Peter G. Jones, Daniel B. Werz
Chemistry - A European Journal (2022) Vol. 29, Iss. 20
Open Access | Times Cited: 9

Metal-free domino Cloke-Wilson rearrangement-hydration-dimerization of cyclopropane carbaldehydes: A facile access to oxybis(2-aryltetrahydrofuran) derivatives
Raghunath Dey, Shruti Rajput, Prabal Banerjee
Tetrahedron (2020) Vol. 76, Iss. 15, pp. 131080-131080
Closed Access | Times Cited: 14

Desymmetrization of 1-Symmetrical Donor–Acceptor (D–A) Cyclopropanes via Reactions with 1,3-Cyclodiones
Dongxin Zhang, Junchao Zhong, Lei Yin, et al.
The Journal of Organic Chemistry (2020) Vol. 85, Iss. 9, pp. 5778-5786
Closed Access | Times Cited: 13

Ring-opening reactions of donor–acceptor cyclopropanes with cyclic ketals and thiol ketals
Dongxin Zhang, Lei Yin, Junchao Zhong, et al.
Organic & Biomolecular Chemistry (2020) Vol. 18, Iss. 33, pp. 6492-6496
Closed Access | Times Cited: 13

Lewis‐Acid‐Catalyzed (3+2)‐Cycloadditions of Donor‐Acceptor Cyclopropanes with Thioketenes
Grzegorz Mlostoń, Mateusz Kowalczyk, André U. Augustin, et al.
European Journal of Organic Chemistry (2021) Vol. 2021, Iss. 46, pp. 6250-6253
Open Access | Times Cited: 12

Donor–Acceptor Bicyclopropyls as 1,6-Zwitterionic Intermediates: Synthesis and Reactions with 4-Phenyl-1,2,4-triazoline-3,5-dione and Terminal Acetylenes
Konstantin V. Potapov, Dmitry A. Denisov, Valeriia V. Glushkova, et al.
The Journal of Organic Chemistry (2020) Vol. 85, Iss. 23, pp. 15562-15576
Closed Access | Times Cited: 12

Synthesis of substituted 1,2-dihydroisoquinolines via Ni(ii) and Cu(i)/Ag(i) catalyzed double nucleophilic addition of arylamines to ortho-alkynyl donor–acceptor cyclopropanes (o-ADACs)
Ramanjaneyulu Unnava, Kapil Chahal, K. Rajender Reddy
Organic & Biomolecular Chemistry (2021) Vol. 19, Iss. 27, pp. 6025-6029
Closed Access | Times Cited: 11

Reversal of regioselectivity in reactions of donor–acceptor cyclopropanes with electrophilic olefins
Joanna Turkowska, Jakub Durka, Michał Ociepa, et al.
Chemical Communications (2021) Vol. 58, Iss. 4, pp. 509-512
Closed Access | Times Cited: 11

Asymmetric ring-opening reactions of donor–acceptor cyclopropanes with 1,3-cyclodiones
Dongxin Zhang, Lvjia Chen, Huiqing Deng, et al.
RSC Advances (2023) Vol. 13, Iss. 11, pp. 7432-7435
Open Access | Times Cited: 4

Electrocatalytic Synthesis of 1,2-Dioxolanes from Tetrasubstituted Donor–Acceptor Cyclopropanes
Gwyndaf A. Oliver, Simon Kolb, Daniel B. Werz
Synlett (2023) Vol. 35, Iss. 09, pp. 963-966
Closed Access | Times Cited: 4

Synthesis of Tetrasubstituted Enamines Using Secondary Amines and In Situ-Generated Allenes from Nitrocyclopropanes
Zhong‐Yang Xu, Jian-Sheng Wei, Li Liu, et al.
The Journal of Organic Chemistry (2024) Vol. 89, Iss. 19, pp. 13868-13875
Closed Access | Times Cited: 1

“Cyclopropanation of Cyclopropanes”: GaCl3-Mediated Ionic Cyclopropanation of Donor–Acceptor Cyclopropanes with Diazo Esters as a Route to Tetrasubstituted Activated Cyclopropanes
I. A. Borisova, Daria-Maria V. Ratova, Konstantin V. Potapov, et al.
The Journal of Organic Chemistry (2021) Vol. 86, Iss. 6, pp. 4567-4579
Closed Access | Times Cited: 10

Synthesis of 1,5-Substituted Pyrrolidin-2-ones from Donor–Acceptor Cyclopropanes and Anilines/Benzylamines
Maksim А. Boichenko, Andrey Yu. Plodukhin, Vitaly V. Shorokhov, et al.
Molecules (2022) Vol. 27, Iss. 23, pp. 8468-8468
Open Access | Times Cited: 7

Understanding the Reactivity of Donor–Acceptor Cyclopropanes: Structural and Electronic Analysis
Anu Jacob, Gwyndaf A. Oliver, Daniel B. Werz
(2024), pp. 15-36
Closed Access | Times Cited: 1

AlCl3‐Promoted Ritter‐Type Ring‐Opening Reactions of γ‐Butyrolactone Fused Donor‐Acceptor Cyclopropanes with Wet Aliphatic Nitriles
V. John Tamilarasan, Kannupal Srinivasan
European Journal of Organic Chemistry (2019) Vol. 2020, Iss. 5, pp. 593-598
Closed Access | Times Cited: 10

Lewis Acid‐Catalyzed Formal (4+2)‐ and (2+2+2)‐Cycloaddition Between 1‐Azadienes and Styrylmalonates as Analogues of Donor‐Acceptor Cyclopropanes
Pavel G. Sergeev, Роман А. Новиков, Yury V. Tomilov
Advanced Synthesis & Catalysis (2021) Vol. 363, Iss. 23, pp. 5292-5299
Closed Access | Times Cited: 8

Transition-Metal-Free [3+2] Dehydration Cycloaddition of Donor-Acceptor Cyclopropanes With 2-Naphthols
Hua Zhao, Peng Shen, Dongru Sun, et al.
Frontiers in Chemistry (2021) Vol. 9
Open Access | Times Cited: 8

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 (2021) Vol. 133, Iss. 49, pp. 26029-26035
Open Access | Times Cited: 8

Lewis acid triggered N-alkylation of sulfoximines through nucleophilic ring-opening of donor–acceptor cyclopropanes: synthesis of γ-sulfoximino malonic diesters
Satish G. More, Gurunath Suryavanshi
Organic & Biomolecular Chemistry (2022) Vol. 20, Iss. 12, pp. 2518-2529
Closed Access | Times Cited: 6

Development of cationic gallium phthalocyanine catalysts for the chemistry of donor-acceptor cyclopropanes and its reactions with aldehydes
Anastasia A. Levina, Роман А. Новиков, Denis D. Borisov, et al.
Molecular Catalysis (2023) Vol. 550, pp. 113480-113480
Closed Access | Times Cited: 3

Cyclopentene Synthesis by a Catalytic [3+2] Annulation of Donor‐Acceptor Cyclopropanes with Polarized Alkenes
Cong Xu, Na Wei, Dongsheng Zhu, et al.
ChemistrySelect (2020) Vol. 5, Iss. 36, pp. 11399-11402
Closed Access | Times Cited: 8

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