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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:

Ugi 4-CR/Pictet–Spengler reaction as a short route to tryptophan-derived peptidomimetics
Giordano Lesma, R. Cecchi, Sergio Crippa, et al.
Organic & Biomolecular Chemistry (2012) Vol. 10, Iss. 45, pp. 9004-9004
Closed Access | Times Cited: 30

Showing 1-25 of 30 citing articles:

Isocyanide-based multicomponent reactions towards cyclic constrained peptidomimetics
Gijs Koopmanschap, Eelco Ruijter, Romano V. A. Orrù
Beilstein Journal of Organic Chemistry (2014) Vol. 10, pp. 544-598
Open Access | Times Cited: 235
Two decades of recent advances of Ugi reactions: synthetic and pharmaceutical applications
Manar Ahmed Fouad, Hamida Abdel‐Hamid, Mohammed Salah Ayoup
RSC Advances (2020) Vol. 10, Iss. 70, pp. 42644-42681
Open Access | Times Cited: 137
Application of Pictet–Spengler Reaction to Indole-Based Alkaloids Containing Tetrahydro-β-carboline Scaffold in Combinatorial Chemistry
R. Nishanth Rao, Barnali Maiti, Kaushik Chanda
ACS Combinatorial Science (2017) Vol. 19, Iss. 4, pp. 199-228
Closed Access | Times Cited: 104
The Pictet-Spengler Reaction Updates Its Habits
Andrea Calcaterra, Laura Mangiardi, Giuliano Delle Monache, et al.
Molecules (2020) Vol. 25, Iss. 2, pp. 414-414
Open Access | Times Cited: 71
Copper(I)‐Catalyzed Three‐Component Coupling of N‐Tosylhydrazones, Alkynes and Azides: Synthesis of Trisubstituted 1,2,3‐Triazoles
Zhikun Zhang, Qi Zhou, Fei Ye, et al.
Advanced Synthesis & Catalysis (2015) Vol. 357, Iss. 10, pp. 2277-2286
Closed Access | Times Cited: 69
Antimicrobial activity of cyclic dipeptides produced by Lactobacillus plantarum LBP-K10 against multidrug-resistant bacteria, pathogenic fungi, and influenza A virus
Min‐Kyu Kwak, Rui Liu, Sa-Ouk Kang
Food Control (2017) Vol. 85, pp. 223-234
Closed Access | Times Cited: 36
Tricycles by a New Ugi Variation and Pictet–Spengler Reaction in One Pot
Mantosh K. Sinha, Kareem Khoury, Eberhardt Herdtweck, et al.
Chemistry - A European Journal (2013) Vol. 19, Iss. 25, pp. 8048-8052
Open Access | Times Cited: 32
Application of the Ugi reaction with multiple amino acid-derived components: synthesis and conformational evaluation of piperazine-based minimalist peptidomimetics
Mattia Stucchi, Silvia Cairati, Rengül Çetin-Atalay, et al.
Organic & Biomolecular Chemistry (2015) Vol. 13, Iss. 17, pp. 4993-5005
Open Access | Times Cited: 26
Diverse Isoquinoline Scaffolds by Ugi/Pomeranz–Fritsch and Ugi/Schlittler–Müller Reactions
Yuanze Wang, Pravin Patil, Katarzyna Kurpiewska, et al.
Organic Letters (2019) Vol. 21, Iss. 10, pp. 3533-3537
Open Access | Times Cited: 23
The high-throughput solid-phase extraction of cis-cyclo(L-Leu-L-Pro) and cis-cyclo(L-Phe-L-Pro) from Lactobacillus plantarum demonstrates efficacy against multidrug-resistant bacteria and influenza A (H3N2) virus
Jaeyoung Son, Yeonju Hong, Hyeri Seong, et al.
Frontiers in Molecular Biosciences (2024) Vol. 11
Open Access | Times Cited: 2
Propargylation of Ugi Amide Dianion: An Entry into Pyrrolidinone and Benzoindolizidine Alkaloid Analogues
Alaa Zidan, Marie Cordier, Abeer M. El‐Naggar, et al.
Organic Letters (2018) Vol. 20, Iss. 9, pp. 2568-2571
Closed Access | Times Cited: 22
Multicomponent access to novel dihydroimidazo[1′,5′:1,2]pyrido[3,4-b]indol-2-ium salts and indoles by means of Ugi/Bischler–Napieralski/heterocyclization two step strategy
Alessandra Silvani, Giordano Lesma, Sergio Crippa, et al.
Tetrahedron (2014) Vol. 70, Iss. 26, pp. 3994-4001
Closed Access | Times Cited: 22
Construction of Highly Functionalized Piperazinones via Post-Ugi Cyclization and Diastereoselective Nucleophilic Addition
Shashank Tripathi, Mayur D. Ambule, Ajay Srivastava
The Journal of Organic Chemistry (2020) Vol. 85, Iss. 11, pp. 6910-6923
Closed Access | Times Cited: 19
Tetrahydro-β-carboline-Based Spirocyclic Lactam as Type II′ β-Turn: Application to the Synthesis and Biological Evaluation of Somatostatine Mimetics
Giordano Lesma, R. Cecchi, Alfredo Cagnotto, et al.
The Journal of Organic Chemistry (2013) Vol. 78, Iss. 6, pp. 2600-2610
Closed Access | Times Cited: 19
Synthesis of 1′-tetrazolylmethyl-spiro[pyrrolidine-3,3′-oxindoles] via two coupled one-pot processes Ugi-azide/Pictet–Spengler and oxidative spiro-rearrangement
Nancy V. Alvarez-Rodríguez, Alejandro Islas‐Jácome, Ángel Rentería‐Gómez, et al.
New Journal of Chemistry (2017) Vol. 42, Iss. 3, pp. 1600-1603
Closed Access | Times Cited: 18
Fishing in the Toolbox of Cyclic Turn Mimics: a Literature Overview of the Last Decade
Raffaella Bucci, Francesca Foschi, Camilla Loro, et al.
European Journal of Organic Chemistry (2021) Vol. 2021, Iss. 20, pp. 2887-2900
Open Access | Times Cited: 14
Isonitrile-Based Multicomponent Synthesis of β-Amino Boronic Acids as β-Lactamase Inhibitors
Emanuele Bassini, Stefano Gazzotti, Filomena Sannio, et al.
Antibiotics (2020) Vol. 9, Iss. 5, pp. 249-249
Open Access | Times Cited: 13
Complementary isonitrile-based multicomponent reactions for the synthesis of diversified cytotoxic hemiasterlin analogues
Giordano Lesma, Ivan Bassanini, Roberta Bortolozzi, et al.
Organic & Biomolecular Chemistry (2015) Vol. 13, Iss. 48, pp. 11633-11644
Open Access | Times Cited: 12
Pictet–Spengler-Based Multicomponent Domino Reactions to Construct Polyheterocycles
Junduo Hu, Liliang Huang, Huangdi Feng
Pharmaceutical Fronts (2023) Vol. 05, Iss. 04, pp. e227-e242
Open Access | Times Cited: 4
Diastereoselective Synthesis of High Functionalized 4‐Imidazolidinone‐Tetrahydro‐beta‐Carboline Hybrids via divergent post‐Ugi Transformation
Valerio Morlacci, Antonio Arcadi, Massimiliano Aschi, et al.
Advanced Synthesis & Catalysis (2024) Vol. 366, Iss. 10, pp. 2376-2381
Open Access | Times Cited: 1
Application of Chiral Isocyanides in Multicomponent Reactions
Vaezeh Fathi Vavsari, Pegah Shakeri, Saeed Balalaie
Current Organic Chemistry (2020) Vol. 24, Iss. 2, pp. 162-183
Closed Access | Times Cited: 10
Multicomponent Synthesis and Biological Evaluation of a Piperazine-Based Dopamine Receptor Ligand Library
Mattia Stucchi, Peter Gmeiner, Harald Huebner, et al.
ACS Medicinal Chemistry Letters (2015) Vol. 6, Iss. 8, pp. 882-887
Open Access | Times Cited: 9
Peptidomimetics II
William D. Lubell
Topics in heterocyclic chemistry (2016)
Closed Access | Times Cited: 6
Rapid access to reverse-turn peptidomimetics by a three-component Ugi reaction of 3,4-dihydroisoquinoline
Arianna Rossetti, Alessandro Sacchetti, Marta Gatti, et al.
Chemistry of Heterocyclic Compounds (2017) Vol. 53, Iss. 11, pp. 1214-1219
Closed Access | Times Cited: 4
Synthesis of rigid tryptophan mimetics by the diastereoselective Pictet-Spengler reaction ofβ3-homo-tryptophan derivatives with chiralα-amino aldehydes
Marta Slupska, Karolina Pułka-Ziach, Edyta Deluga, et al.
Journal of Peptide Science (2015) Vol. 21, Iss. 12, pp. 893-904
Closed Access | Times Cited: 2
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