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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:

Facile synthesis of diverse isoindolinone derivatives via Ugi-4CR followed by Cu-catalyzed deamidative C(sp2)–C(sp3) coupling
Vikas Tyagi, Shahnawaz Khan, Prem M. S. Chauhan
Tetrahedron Letters (2012) Vol. 54, Iss. 10, pp. 1279-1284
Closed Access | Times Cited: 32

Showing 1-25 of 32 citing articles:

Divergent Palladium Iodide Catalyzed Multicomponent Carbonylative Approaches to Functionalized Isoindolinone and Isobenzofuranimine Derivatives
Raffaella Mancuso, Ida Ziccarelli, Donatella Armentano, et al.
The Journal of Organic Chemistry (2014) Vol. 79, Iss. 8, pp. 3506-3518
Closed Access | Times Cited: 96
Isoindolinone Synthesis via One‐Pot Type Transition Metal Catalyzed C−C Bond Forming Reactions
Risto Savela, Carolina Méndez‐Gálvez
Chemistry - A European Journal (2020) Vol. 27, Iss. 17, pp. 5344-5378
Open Access | Times Cited: 62
A crystalline Sm(III)-containing antimonotungstate with efficient catalytic activity in three-component reaction for isoindolinones synthesis
Hao-Qi Liu, Jiawei Cao, Wei Tang, et al.
Rare Metals (2025)
Closed Access
Organocatalysts and sequential asymmetric cascade reactions in the synthesis of functionalized isoindolinones and benzoindolizidinones
Silvia Tiso, Laura Palombi, Chiara Vignes, et al.
RSC Advances (2013) Vol. 3, Iss. 42, pp. 19380-19380
Closed Access | Times Cited: 41
One-pot synthesis of spiropyrroloquinoline-isoindolinone and their aza-analogs via the Ugi-4CR/metal-free intramolecular bis-annulation process
Mehdi Ghandi, Nahid Zarezadeh, Alireza Abbasi
Organic & Biomolecular Chemistry (2015) Vol. 13, Iss. 30, pp. 8211-8220
Closed Access | Times Cited: 38
Synthesis of various N-heterocycles using the four-component Ugi reaction
Majid Μ. Heravi, Leyla Mohammadkhani
Advances in heterocyclic chemistry (2019), pp. 351-403
Open Access | Times Cited: 32
Ultrasound mediation for one-pot multi-component synthesis of amidoalkyl naphthols using new magnetic nanoparticles modified by ionic liquids
Javad Safari, Zohre Zarnegar
Ultrasonics Sonochemistry (2013) Vol. 21, Iss. 3, pp. 1132-1139
Closed Access | Times Cited: 30
Diversity oriented synthesis of β-carbolinone and indolo-pyrazinone analogues based on an Ugi four component reaction and subsequent cyclisation of the resulting indole intermediate
Pooja Purohit, Anand Kumar Pandey, Brijesh Kumar, et al.
RSC Advances (2016) Vol. 6, Iss. 25, pp. 21165-21186
Closed Access | Times Cited: 23
Facile synthesis of functionalized 1H-pyrrolo[2,3-b]quinolines via Ugi four-component reaction followed by Cu-catalyzed aryl-amide, C–N bond coupling
Mrityunjaya Asthana, Ritush Kumar, Tanu Gupta, et al.
Tetrahedron Letters (2015) Vol. 56, Iss. 7, pp. 907-912
Closed Access | Times Cited: 24
Synthesis of Polysubstituted Isoindolinones via Radical Cyclization of 1,3-Dicarbonyl Ugi-4CR Adducts Using Tetrabutylammonium Persulfate and TEMPO
Andrés Borja‐Miranda, Fabiola Valencia-Villegas, J. Armando Luján‐Montelongo, et al.
The Journal of Organic Chemistry (2020) Vol. 86, Iss. 1, pp. 929-946
Closed Access | Times Cited: 20
An efficient microwave-assisted synthesis of cotinine and iso-cotinine analogs from an Ugi-4CR approach
Luis A. Polindara‐García, Dario Montesinos‐Miguel, Alfredo Vázquez
Organic & Biomolecular Chemistry (2015) Vol. 13, Iss. 34, pp. 9065-9071
Closed Access | Times Cited: 19
Post-Ugi carbocyclization/fragmentation sequence for the synthesis of 6,7-dihydro-5H-pyrrolo[3,4-b]pyridin-5-ones
Trần Thị Thu Trang, Anatoly A. Peshkov, Jeroen Jacobs, et al.
Tetrahedron Letters (2015) Vol. 56, Iss. 22, pp. 2882-2886
Closed Access | Times Cited: 19
Gold‐Catalyzed Post‐Ugi Cascade Transformation for the Synthesis of 2‐Pyridones
Xiaochen Du, Jiafeng Yu, Jing Gong, et al.
European Journal of Organic Chemistry (2019) Vol. 2019, Iss. 14, pp. 2502-2507
Closed Access | Times Cited: 17
Stefano Marcaccini: a pioneer in isocyanide chemistry
Ana G. Neo, José Luis Ramiro, María García‐Valverde, et al.
Molecular Diversity (2023) Vol. 28, Iss. 1, pp. 335-418
Open Access | Times Cited: 5
Propylphosphonic anhydride (T3P®) mediated synthesis of 3-oxoisoindoline-1-carboxamides from 2-formylbenzoic acid, amines, and isocyanides. Preparation of isoindolinone alkaloids
Valentina Varga, Mátyás Milen, Péter Ábrányi‐Balogh
Tetrahedron Letters (2018) Vol. 59, Iss. 41, pp. 3683-3689
Closed Access | Times Cited: 15
One-pot synthesis of 2-arylbenzoxazole derivatives via Cu(I) catalyzed C–N/C–O coupling of N-(2-chloro-phenyl)-2-halo-benzamides and primary amines
Dazhuang Miao, Xuesong Shi, Guozhen He, et al.
Tetrahedron (2014) Vol. 71, Iss. 3, pp. 431-435
Closed Access | Times Cited: 15
Straightforward access to complex isoindolinones from the Ugi reaction of o-nitrobenzoic acid derivatives
Mahanandaiah Kurva, Mansour Dolé Kerim, Rocío Gámez‐Montaño, et al.
Organic & Biomolecular Chemistry (2019) Vol. 17, Iss. 44, pp. 9655-9659
Open Access | Times Cited: 15
Chiral Phase Transfer Catalysts for the Synthesis of Chiral N‐Heterocycles viaAsymmetric Cascade Reactions
Silvia Tiso, António Massa
Journal of Heterocyclic Chemistry (2014) Vol. 52, Iss. 5, pp. 1570-1575
Closed Access | Times Cited: 13
Palladium-catalyzed highly chemoselective dearomative spirocyclization of Ugi adducts: facile access to functionalized benzoazepinespiroindolenines with diastereoselectivity
Chuan‐Hua Qu, Shu-Ting Li, Jianbo Liu, et al.
Organic Chemistry Frontiers (2023) Vol. 10, Iss. 20, pp. 5083-5091
Closed Access | Times Cited: 4
An efficient and practical approach for the synthesis of indoloquinolines and indolo/pyrroloquinoxalines via a Cu-catalyzed Ugi-C/Ugi-N-arylation sequence
Sheiva Iranfar, Morteza Shiri, Yazdanbakhsh Lotfi Nosood, et al.
RSC Advances (2024) Vol. 14, Iss. 26, pp. 18271-18276
Open Access | Times Cited: 1
Facile ligand-free Pd-catalyzed tandem C–C/C–N coupling reaction: a novel access to highly diverse tetrazole tag isoindoline derivatives
Moni Sharma, Irfan Khan, Shahnawaz Khan, et al.
Tetrahedron Letters (2015) Vol. 56, Iss. 40, pp. 5401-5408
Closed Access | Times Cited: 11
Raising the Diversity of Ugi Reactions Through Selective Alkylations and Allylations of Ugi Adducts
Alaa Zidan, Abeer M. El‐Naggar, Nour E. A. Abd El‐Sattar, et al.
Frontiers in Chemistry (2019) Vol. 7
Open Access | Times Cited: 10
Palladium-Catalyzed Cross-Coupling Reactions of Potassium N-Methyltrifluoroborate Isoindolin-1-one with Aryl and Heteroaryl Chlorides
Rashid N. Nadaf, Dave G. Seapy
Synthetic Communications (2014) Vol. 44, Iss. 14, pp. 2012-2020
Open Access | Times Cited: 5
Convenient synthesis of benzothiazinoisoindol-11-ones and benzoindenothiazin-11-ones, and antimicrobial testing thereof
Satbir Mor, Mohini Khatri
Molecular Diversity (2022) Vol. 27, Iss. 3, pp. 1223-1241
Closed Access | Times Cited: 4
Triflic-acid promoted post-Ugi condensation for the assembly of 2,6-diarylmorpholin-3-ones
Niyaz Amire, Kamila M. Almagambetova, Assel Turlykul, et al.
Organic & Biomolecular Chemistry (2024)
Closed Access
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