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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:

Stereoselective thia‐Michael 1,4‐Addition to Acyclic 2,4‐Dienones and 2‐En‐4‐ynones
Rafał Kowalczyk, Przemysław J. Boratyński
Advanced Synthesis & Catalysis (2016) Vol. 358, Iss. 8, pp. 1289-1295
Closed Access | Times Cited: 20

Showing 20 citing articles:

Palladium-Catalyzed Oxidative Allylation of Sulfoxonium Ylides: Regioselective Synthesis of Conjugated Dienones
Chunsheng Li, Meng Li, Wentao Zhong, et al.
Organic Letters (2019) Vol. 21, Iss. 4, pp. 872-875
Closed Access | Times Cited: 72
Cooperative Palladium/Isothiourea Catalyzed Enantioselective Formal (3+2) Cycloaddition of Vinylcyclopropanes and α,β‐Unsaturated Esters
Jacqueline Bitai, Alastair J. Nimmo, Alexandra M. Z. Slawin, et al.
Angewandte Chemie International Edition (2022) Vol. 61, Iss. 25
Open Access | Times Cited: 33
Tertiary Amine-Derived Ionic Liquid-Supported Squaramide as a Recyclable Organocatalyst for Noncovalent “On Water” Catalysis
Rinat S. Tukhvatshin, Alexander S. Kucherenko, Yulia V. Nelyubina, et al.
ACS Catalysis (2017) Vol. 7, Iss. 4, pp. 2981-2989
Closed Access | Times Cited: 59
Aryloxide-Facilitated Catalyst Turnover in Enantioselective α,β-Unsaturated Acyl Ammonium Catalysis
Anastassia Matviitsuk, Mark D. Greenhalgh, Diego‐Javier Barrios Antúnez, et al.
Angewandte Chemie International Edition (2017) Vol. 56, Iss. 40, pp. 12282-12287
Open Access | Times Cited: 53
Conjugated enynones: preparation, properties and applications in organic synthesis
А. А. Голованов, Иван С. Один, Simon S. Zlotskii
Russian Chemical Reviews (2018) Vol. 88, Iss. 3, pp. 280-318
Closed Access | Times Cited: 39
Mechanochemical Assisted Chemoselective and Stereoselective Hydrogen‐Bonding Catalyzed Addition of Dithiomalonates to Enones
Żaneta A. Mała, Mikołaj J. Janicki, Robert W. Góra, et al.
Advanced Synthesis & Catalysis (2023) Vol. 365, Iss. 19, pp. 3342-3352
Open Access | Times Cited: 7
Applications of Thermal Activation, Ball‐milling and Aqueous Medium in Stereoselective Michael Addition of Nitromethane to Enynones Catalyzed by Chiral Squaramides
Żaneta Anna Ignatiuk, Mikołaj J. Janicki, Robert W. Góra, et al.
Advanced Synthesis & Catalysis (2019) Vol. 361, Iss. 5, pp. 1108-1116
Closed Access | Times Cited: 21
Aryloxide‐Facilitated Catalyst Turnover in Enantioselective α,β‐Unsaturated Acyl Ammonium Catalysis
Anastassia Matviitsuk, Mark D. Greenhalgh, Diego‐Javier Barrios Antúnez, et al.
Angewandte Chemie (2017) Vol. 129, Iss. 40, pp. 12450-12455
Open Access | Times Cited: 18
The chemistry of the carbon-transition metal double and triple bond: Annual survey covering the year 2016
James W. Herndon
Coordination Chemistry Reviews (2017) Vol. 356, pp. 1-114
Closed Access | Times Cited: 16
Organocatalytic Strategy for a Formal 1,6-Conjugate Hydroxylation
Sifeddine Mohamed Aouina, Anthony Lapray, Jean‐Valère Naubron, et al.
Organic Letters (2024) Vol. 26, Iss. 43, pp. 9294-9298
Closed Access | Times Cited: 1
Organocatalytic Enantioselective Tandem Michael Addition and Cyclization Reaction of Trisubstituted 2‐Nitro‐1,3‐enynes with Cyclic 1,3‐Diketones
Zi‐Min Xing, Le‐Le Song, Feng‐Xing Li, et al.
Advanced Synthesis & Catalysis (2017) Vol. 359, Iss. 11, pp. 1892-1900
Closed Access | Times Cited: 11
Multicomponent reaction of conjugated enynones with malononitrile and sodium alkoxides: Complex reaction mechanism of the formation of pyridine derivatives
Anastasiya V. Kuznetcova, Иван С. Один, А. А. Голованов, et al.
Tetrahedron (2019) Vol. 75, Iss. 33, pp. 4516-4530
Closed Access | Times Cited: 11
Reactions of linear conjugated dienone structures with arenes under superelectrophilic activation conditions. An experimental and theoretical study of intermediate multicentered electrophilic species
Matvei A. Kochurin, Alina Ismagilova, Dmitriy N. Zakusilo, et al.
New Journal of Chemistry (2022) Vol. 46, Iss. 25, pp. 12041-12053
Closed Access | Times Cited: 7
Enyne Meldrum´s acid derivatives: synthesis and Michael reactions with amines and thiols
S. A. Sokov, Иван С. Один, Dmitry M. Gusev, et al.
Russian Chemical Bulletin (2020) Vol. 69, Iss. 2, pp. 305-312
Closed Access | Times Cited: 8
Cooperative Palladium/Isothiourea Catalyzed Enantioselective Formal (3+2) Cycloaddition of Vinylcyclopropanes and α,β‐Unsaturated Esters
Jacqueline Bitai, Alastair J. Nimmo, Alexandra M. Z. Slawin, et al.
Angewandte Chemie (2022) Vol. 134, Iss. 25
Open Access | Times Cited: 4
C3‐Thioester/‐Ester Substituted Linear Dienones: A Pluripotent Molecular Platform for Diversification via Cascade Pericyclic Reactions
Abhijit Bankura, Sandip Naskar, Sabyasachi Roy Chowdhury, et al.
Advanced Synthesis & Catalysis (2020) Vol. 362, Iss. 17, pp. 3604-3612
Closed Access | Times Cited: 4
Zinc complexes supported by pyridine-N-oxide ligands: synthesis, structures and catalytic Michael addition reactions
Xiu‐Fang Mo, Chang-Feng Xiong, Zewen Chen, et al.
Dalton Transactions (2020) Vol. 49, Iss. 35, pp. 12365-12371
Closed Access | Times Cited: 3
ChemInform Abstract: Stereoselective thia‐Michael 1,4‐Addition to Acyclic 2,4‐Dienones and 2‐En‐4‐ynones.
Rafał Kowalczyk, Przemysław J. Boratyński
ChemInform (2016) Vol. 47, Iss. 37
Closed Access
Regiospecific 1,4-Michael Addition of Phenylacetonitrile to 1,5-Diarylpenta-2,4-Dien-1-Ones
Zheng Li, Wenli Song
Journal of Chemical Research (2018) Vol. 42, Iss. 7, pp. 347-349
Open Access
Some Features of the Reactions of 3-Nitro-6-phenylhexa-3,5-dien-2-one with Thiophenols
Р. И. Байчурин, Vladislav Sergeev, N. I. Aboskalova, et al.
Russian Journal of General Chemistry (2020) Vol. 90, Iss. 5, pp. 769-772
Closed Access
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