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:

An effective one-pot access to polynuclear dispiroheterocyclic structures comprising pyrrolidinyloxindole and imidazothiazolotriazine moieties via a 1,3-dipolar cycloaddition strategy
Alexei N. Izmest’ev, Галина А. Газиева, Natalya V. Sigay, et al.
Beilstein Journal of Organic Chemistry (2016) Vol. 12, pp. 2240-2249
Open Access | Times Cited: 21

Showing 21 citing articles:

Progress in the chemistry of nitrogen-, oxygen- and sulfur-containing heterocyclic systems
Нина Н. Махова, Л. И. Беленький, Галина А. Газиева, et al.
Russian Chemical Reviews (2019) Vol. 89, Iss. 1, pp. 55-124
Closed Access | Times Cited: 130

Engaging Isatins in Multicomponent Reactions (MCRs) – Easy Access to Structural Diversity
Pedro Brandão, Carolina S. Marques, Elisabete P. Carreiro, et al.
The Chemical Record (2021) Vol. 21, Iss. 4, pp. 924-1037
Open Access | Times Cited: 43

Classical and interdisciplinary approaches to the design of organic and hybrid molecular systems
A. N. Vereshchagin
Russian Chemical Bulletin (2017) Vol. 66, Iss. 10, pp. 1765-1796
Closed Access | Times Cited: 31

Asymmetric Metal‐Templated Route to Amino Acids with 3‐Spiropyrrolidine Oxindole Core via a 1,3‐Dipolar Addition of Azomethine Ylides to a Chiral Dehydroalanine Ni(II) Complex
Zalina T. Gugkaeva, Maria V. Panova, Alexander F. Smol’yakov, et al.
Advanced Synthesis & Catalysis (2022) Vol. 364, Iss. 14, pp. 2395-2402
Closed Access | Times Cited: 16

Substrate‐Controlled Regioselectivity Switch in a Three‐Component 1,3‐Dipolar Cycloaddition Reaction to Access 3,3′‐Pyrrolidinyl‐Spirooxindoles Derivatives
Kai‐Kai Wang, Yan‐Li Li, Rongxiang Chen, et al.
Advanced Synthesis & Catalysis (2022) Vol. 364, Iss. 12, pp. 2047-2052
Closed Access | Times Cited: 15

Substrate-Controlled Regioselectivity Switchable [3 + 2] Annulations To Access Spirooxindole Skeletons
Kai‐Kai Wang, Yanli Li, Rongxiang Chen, et al.
The Journal of Organic Chemistry (2022) Vol. 87, Iss. 12, pp. 8158-8169
Closed Access | Times Cited: 14

Recognition of arylmethylidene derivatives of imidazothiazolotriazinones as novel tubulin polymerization inhibitors
Alexei N. Izmest’ev, E. V. Svirshchevskaya, Sergey B. Akopov, et al.
RSC Medicinal Chemistry (2024) Vol. 15, Iss. 4, pp. 1258-1273
Closed Access | Times Cited: 2

Synthesis of spiropyrrolidine oxindolesviaAg-catalyzed stereo- and regioselective 1,3-dipolar cycloaddition of indole-based azomethine ylides with chalcones
Guizhou Yue, Yao Wu, Zhengjie Dou, et al.
New Journal of Chemistry (2018) Vol. 42, Iss. 24, pp. 20024-20031
Closed Access | Times Cited: 17

Diastereodivergent synthesis of dispiroheterocyclic structures comprising pyrrolidinyloxindole and imidazothiazolotriazine moieties
Alexei N. Izmest’ev, Галина А. Газиева, Валентина А. Карноухова, et al.
Organic & Biomolecular Chemistry (2020) Vol. 18, Iss. 35, pp. 6905-6911
Closed Access | Times Cited: 13

5‐Indolylidene‐2‐iminothiazolidin‐4‐ones – Convenient Starting Compounds for Stereoselective Synthesis of Novel Dispirooxindole Derivatives
Alexei N. Izmest’ev, Andrey А. Streltsov, Валентина А. Карноухова, et al.
ChemistrySelect (2022) Vol. 7, Iss. 2
Closed Access | Times Cited: 8

Skeletal rearrangement of arylmethylideneimidazo[4,5-e]thiazolo[3,2-b]-1,2,4-triazine-2,7-diones in the synthesis of the corresponding imidazo[4,5-e]thiazolo[2,3-c]-1,2,4-triazine-2,8-diones
Alexei N. Izmest’ev, Darya A. Vasileva, Elizaveta K. Melnikova, et al.
New Journal of Chemistry (2018) Vol. 43, Iss. 2, pp. 1038-1052
Closed Access | Times Cited: 13

Cascade of Michael Addition/Retro‐Michael Reaction/Skeletal Rearrangement in the Synthesis of Arylmethylidene Derivatives of Imidazothiazolotriazines
Alexei N. Izmest’ev, Nikita A. Kim, Валентина А. Карноухова, et al.
ChemistrySelect (2019) Vol. 4, Iss. 35, pp. 10483-10487
Closed Access | Times Cited: 12

Synthesis and cytotoxicity of oxindoles dispiro derivatives with thiohydantoin and adamantane fragments
Maxim E. Kukushkin, Dmitriy A. Skvortsov, Marina Kalinina, et al.
Phosphorus, sulfur, and silicon and the related elements (2020) Vol. 195, Iss. 7, pp. 544-555
Closed Access | Times Cited: 11

Tandem Michael addition/elimination – novel reactivity of pyridinium ylides in reaction with electron-deficient alkenes
Alexei N. Izmest’ev, Vladimir Motornov, Dmitry B. Vinogradov, et al.
Organic Chemistry Frontiers (2022) Vol. 9, Iss. 18, pp. 4998-5004
Closed Access | Times Cited: 7

1,2,4-Triazines and Their Benzo Derivatives
Sergey M. Ivanov
Elsevier eBooks (2021), pp. 29-180
Closed Access | Times Cited: 8

A Diastereoselective Synthesis of Dispiro[oxindole-cyclohexanone]pyrrolidines by 1,3-Dipolar Cycloaddition
А. А. Аниськов, И. Н. Клочкова, Roman S. Tumskiy, et al.
Molecules (2017) Vol. 22, Iss. 12, pp. 2134-2134
Open Access | Times Cited: 4

Synthesis, Structure and Stereochemistry of Dispirocompounds Based on Imidazothiazolotriazine and Pyrrolidineoxindole
Alexei N. Izmest’ev, Валентина А. Карноухова, Alexander А. Larin, et al.
International Journal of Molecular Sciences (2022) Vol. 23, Iss. 22, pp. 13820-13820
Open Access | Times Cited: 3

A Sequential Nitro‐Michael Addition and Reductive Cyclization Cascade Reaction for Diastereoselective Synthesis of Multifunctionalized 3,3'‐pyrrolidinyl‐spirooxindoles
Chandrakant B. Nichinde, Meema Bhati, Amardipsing S. Girase, et al.
European Journal of Organic Chemistry (2024) Vol. 28, Iss. 5
Closed Access

Diastereoselective Synthesis of Dispiro[Imidazothiazolotriazine-Pyrrolidin-Oxindoles] and Their Isomerization Pathways in Basic Medium
Alexei N. Izmest’ev, Dmitry B. Vinogradov, Ангелина Н. Кравченко, et al.
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 22, pp. 16359-16359
Open Access | Times Cited: 1

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