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:

A highly diastereoselective one-pot three-component 1,3-dipolar cycloaddition of cyclopropenes with azomethine ylides generated from 11H-indeno[1,2-b]-quinoxalin-11-ones
Alexander S. Filatov, Nickolay A. Knyazev, Mikhail N. Ryazantsev, et al.
Organic Chemistry Frontiers (2017) Vol. 5, Iss. 4, pp. 595-605
Closed Access | Times Cited: 43

Showing 1-25 of 43 citing articles:

Recent developments in cyclopropene chemistry
Penghua Li, Xiaoyu Zhang, Min Shi
Chemical Communications (2020) Vol. 56, Iss. 41, pp. 5457-5471
Closed Access | Times Cited: 94
Synthesis of bicyclo[3.1.0]hexanes by (3 + 2) annulation of cyclopropenes with aminocyclopropanes
Bastian Muriel, Alec Gagnebin, Jérôme Waser
Chemical Science (2019) Vol. 10, Iss. 46, pp. 10716-10722
Open Access | Times Cited: 81
Highly Efficient Synthesis of Spiro[1-azabicyclo[3.2.0]heptane] Frameworks via [3+2]-Cycloaddition
Yulia A. Pronina, Alexander S. Filatov, Stanislav V. Shmakov, et al.
The Journal of Organic Chemistry (2025)
Closed Access | Times Cited: 1
Recent Advances on Diverse Decarboxylative Reactions of Amino Acids
Matiur Rahman, Anindita Mukherjee, Igor S. Коvalev, et al.
Advanced Synthesis & Catalysis (2018) Vol. 361, Iss. 10, pp. 2161-2214
Closed Access | Times Cited: 82
Synthetic Applications of Cyclopropene and Cyclopropenone: Recent Progress and Developments
Bishnu Prasad Raiguru, Sabita Nayak, Deepak Ranjan Mishra, et al.
Asian Journal of Organic Chemistry (2020) Vol. 9, Iss. 8, pp. 1088-1132
Closed Access | Times Cited: 60
Recent advancement in the synthesis of diverse spiro-indeno[1,2-b]quinoxalines: a review
Ruby Singh, Diksha Bhardwaj, Munna Ram Saini
RSC Advances (2021) Vol. 11, Iss. 8, pp. 4760-4804
Open Access | Times Cited: 42
N‐Terminal‐Specific Dual Modification of Peptides through Copper‐Catalyzed [3+2] Cycloaddition
Haruka Machida, Kazuya Kanemoto
Angewandte Chemie International Edition (2024) Vol. 63, Iss. 12
Open Access | Times Cited: 7
Copper(I)-catalyzed asymmetric 1,3-dipolar cycloaddition of 1,3-enynes and azomethine ylides
Boran Wang, Yanbo Li, Qi Zhang, et al.
Nature Communications (2023) Vol. 14, Iss. 1
Open Access | Times Cited: 13
Stereo- and Regioselective 1,3-Dipolar Cycloaddition of the Stable Ninhydrin-Derived Azomethine Ylide to Cyclopropenes: Trapping of Unstable Cyclopropene Dipolarophiles
Alexander S. Filatov, Siqi Wang, Olesya V. Khoroshilova, et al.
The Journal of Organic Chemistry (2019) Vol. 84, Iss. 11, pp. 7017-7036
Closed Access | Times Cited: 42
Asymmetric Construction of 3-Azabicyclo[3.1.0]hexane Skeleton with Five Contiguous Stereogenic Centers by Cu-Catalyzed 1,3-Dipolar Cycloaddition of Trisubstituted Cyclopropenes
Hua Deng, Wu‐Lin Yang, Fei Tian, et al.
Organic Letters (2018) Vol. 20, Iss. 13, pp. 4121-4125
Closed Access | Times Cited: 41
Construction of heterocyclic rings from cyclopropenes
Hengrui Huo, Yuefa Gong
Organic & Biomolecular Chemistry (2022) Vol. 20, Iss. 19, pp. 3847-3869
Closed Access | Times Cited: 22
Cyclopropenes and methylenecyclopropanes in 1,3-dipolar cycloaddition reactions
А. П. Молчанов, Мария М. Ефремова, Михаил А. Кузнецов
Russian Chemical Bulletin (2022) Vol. 71, Iss. 4, pp. 620-650
Closed Access | Times Cited: 19
Study of Cytotoxicity of 3-Azabicyclo[3.1.0]hexanes and Cyclopropa[a]pyrrolizidines Spiro-Fused to Acenaphthylene-1(2H)-one and Aceanthrylene-1(2H)-one Fragments Against Tumor Cell Lines
Anton A. Kornev, Stanislav V. Shmakov, Alexandra M. Gryschenko, et al.
International Journal of Molecular Sciences (2025) Vol. 26, Iss. 8, pp. 3474-3474
Open Access
Organic Chemistry in Russian Universities. Achievements of Recent Years
Ivan I. Stoikov, И. С. Антипин, В. А. Бурилов, et al.
Russian Journal of Organic Chemistry (2024) Vol. 60, Iss. 8, pp. 1361-1584
Closed Access | Times Cited: 3
One pot, three component 1,3 dipolar cycloaddition: Regio and diastereoselective synthesis of spiropyrrolidinyl indenoquinoxaline derivatives
Priyabrata Pattanaik, Sabita Nayak, Deepak Ranjan Mishra, et al.
Tetrahedron Letters (2018) Vol. 59, Iss. 27, pp. 2688-2694
Closed Access | Times Cited: 24
Identification of Spiro-Fused [3-azabicyclo[3.1.0]hexane]oxindoles as Potential Antitumor Agents: Initial In Vitro Evaluation of Anti-Proliferative Effect and Actin Cytoskeleton Transformation in 3T3 and 3T3-SV40 Fibroblast
Nickolay A. Knyazev, Stanislav V. Shmakov, Sofia A. Pechkovskaya, et al.
International Journal of Molecular Sciences (2021) Vol. 22, Iss. 15, pp. 8264-8264
Open Access | Times Cited: 18
Study of Cytotoxicity of Spiro-Fused [3-Azabicyclo[3.1.0]hexane]oxindoles and Cyclopropa[a]pyrrolizidine-oxindoles Against Tumor Cell Lines
Anton A. Kornev, Stanislav V. Shmakov, Alexander I. Ponyaev, et al.
Pharmaceuticals (2024) Vol. 17, Iss. 12, pp. 1582-1582
Open Access | Times Cited: 2
Biological Evaluation of 3-Azaspiro[Bicyclo[3.1.0]Hexane-2,5′-Pyrimidines] as Potential Antitumor Agents
Stanislav V. Shmakov, Diana K. Latypova, Tatiana V. Shmakova, et al.
International Journal of Molecular Sciences (2022) Vol. 23, Iss. 18, pp. 10759-10759
Open Access | Times Cited: 12
Organocatalytic Diastereoselective Synthesis of Spiro[3-azabicyclo[3.1.0]hexanes] via 1,3-Dipolar Cycloaddition of Azomethine Ylides with Cyclopropenes
Yulia A. Pronina, Н. Б. Викторов, Stanislav I. Selivanov, et al.
Russian Journal of General Chemistry (2024) Vol. 94, Iss. 4, pp. 804-823
Closed Access | Times Cited: 2
An expedient synthesis of novel spiro[indenoquinoxaline-pyrrolizidine]-pyrazole conjugates with anticancer activity from 1,5-diarylpent-4-ene-1,3-diones through the 1,3-dipolar cycloaddition/cyclocondensation sequence
Nikolay S. Zimnitskiy, Alexey Yu. Barkov, Maria V. Ulitko, et al.
New Journal of Chemistry (2020) Vol. 44, Iss. 37, pp. 16185-16199
Closed Access | Times Cited: 18
Identification of Spiro-Fused Pyrrolo[3,4-a]pyrrolizines and Tryptanthrines as Potential Antitumor Agents: Synthesis and In Vitro Evaluation
Diana K. Latypova, Stanislav V. Shmakov, Sofia A. Pechkovskaya, et al.
International Journal of Molecular Sciences (2021) Vol. 22, Iss. 21, pp. 11997-11997
Open Access | Times Cited: 15
Synthesis of bis-spirocyclic derivatives of 3-azabicyclo[3.1.0]hexane via cyclopropene cycloadditions to the stable azomethine ylide derived from Ruhemann's purple
Alexander S. Filatov, Olesya V. Khoroshilova, Anna G. Larina, et al.
Beilstein Journal of Organic Chemistry (2022) Vol. 18, pp. 769-780
Open Access | Times Cited: 10
An Experimental and Theoretical Study of the 1,3-Dipolar Cyclo­addition of Alloxan-Derived Azomethine Ylides to Cyclopropenes
Vitaly M. Boitsov, Alexander V. Stepakov, Alexander S. Filatov, et al.
Synthesis (2021) Vol. 54, Iss. 07, pp. 1803-1816
Closed Access | Times Cited: 12
11H-Benzo[4,5]imidazo[1,2-a]indol-11-one as a New Precursor of Azomethine Ylides: 1,3-Dipolar Cycloaddition Reactions with Cyclopropenes and Maleimides
Alexander S. Filatov, Yulia A. Pronina, Stanislav I. Selivanov, et al.
International Journal of Molecular Sciences (2022) Vol. 23, Iss. 21, pp. 13202-13202
Open Access | Times Cited: 8
Cu(I)-Catalyzed Intramolecular Tandem Cyclization of N-Indole-Tethered Cyclopropenes: Synthesis of Functionalized Hydrogenated Diazabenzo[a]cyclopenta[cd]azulene Derivatives
Penghua Li, Song Yang, Tonggang Hao, et al.
Organic Letters (2019) Vol. 21, Iss. 9, pp. 3162-3166
Closed Access | Times Cited: 13
Page 1 - Next Page

Scroll to top