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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:

Applications of Convertible Isonitriles in the Ligation and Macrocyclization of Multicomponent Reaction-Derived Peptides and Depsipeptides
Ludger A. Wessjohann, Micjel Chávez Morejón, Gerardo M. Ojeda‐Carralero, et al.
The Journal of Organic Chemistry (2016) Vol. 81, Iss. 15, pp. 6535-6545
Closed Access | Times Cited: 20

Showing 20 citing articles:

Multicomponent Reaction Toolbox for Peptide Macrocyclization and Stapling
Leslie Reguera, Daniel G. Rivera
Chemical Reviews (2019) Vol. 119, Iss. 17, pp. 9836-9860
Closed Access | Times Cited: 264
Multicomponent Reactions in Ligation and Bioconjugation Chemistry
Leslie Reguera, Yanira Méndez, Ana R. Humpierre, et al.
Accounts of Chemical Research (2018) Vol. 51, Iss. 6, pp. 1475-1486
Closed Access | Times Cited: 115
Peptide Bond-Forming Reaction via Amino Acid Silyl Esters: New Catalytic Reactivity of an Aminosilane
Wataru Muramatsu, Manthena Chaitanya, Erika Nakashima, et al.
ACS Catalysis (2020) Vol. 10, Iss. 16, pp. 9594-9603
Closed Access | Times Cited: 51
Chemical Conjugation in Drug Delivery Systems
Alexis Eras, Danna Castillo, Margarita Suárez, et al.
Frontiers in Chemistry (2022) Vol. 10
Open Access | Times Cited: 32
Unlocking Enol-Ugi-Derived Conformationally Restricted Peptidomimetic Motifs
José Luis Ramiro, Jesús Dı́az, Ana G. Neo, et al.
The Journal of Organic Chemistry (2025)
Closed Access
Exploitation of the Ugi–Joullié reaction in drug discovery and development
Stefano Gazzotti, Giulia Rainoldi, Alessandra Silvani
Expert Opinion on Drug Discovery (2019) Vol. 14, Iss. 7, pp. 639-652
Closed Access | Times Cited: 25
Synthesis of a tubugi-1-toxin conjugate by a modulizable disulfide linker system with a neuropeptide Y analogue showing selectivity for hY1R-overexpressing tumor cells
Rainer Kufka, Robert C. Rennert, Goran N. Kaluđerović, et al.
Beilstein Journal of Organic Chemistry (2019) Vol. 15, pp. 96-105
Open Access | Times Cited: 15
Efficient one-pot synthesis of enantiomerically pure N-protected-α-substituted piperazines from readily available α-amino acids
Mouhamad Jida, Steven Ballet
New Journal of Chemistry (2018) Vol. 42, Iss. 3, pp. 1595-1599
Closed Access | Times Cited: 14
Diversity Driven Decoration and Ligation of Fullerene by Ugi and Passerini Multicomponent Reactions
Bruno B. Ravanello, Nalin Seixas, Oscar E. D. Rodrigues, et al.
Chemistry - A European Journal (2018) Vol. 24, Iss. 39, pp. 9788-9793
Closed Access | Times Cited: 13
Spin-labelled diketopiperazines and peptide–peptoid chimera by Ugi-multi-component-reactions
Haider N. Sultani, Haleh Hashemi Haeri, Dariush Hinderberger, et al.
Organic & Biomolecular Chemistry (2016) Vol. 14, Iss. 48, pp. 11336-11341
Open Access | Times Cited: 12
2‐Nitrobenzyl Isocyanide as a Universal Convertible Isocyanide
Ajay L. Chandgude, Jingyao Li, Alexander Dömlingꝉ
Asian Journal of Organic Chemistry (2017) Vol. 6, Iss. 7, pp. 798-801
Open Access | Times Cited: 12
Multicomponent synthesis of α-acylamino and α-acyloxy amide derivatives of desmycosin and their activity against gram-negative bacteria
Tuvshinjargal Budragchaa, Bernhard Westermann, Ludger A. Wessjohann
Bioorganic & Medicinal Chemistry (2019) Vol. 27, Iss. 15, pp. 3237-3247
Closed Access | Times Cited: 11
A versatile approach to hybrid thiadiazine-based molecules by the Ugi four-component reaction
Radell Echemendía, Olivia Fernandez‐Delgado, Julieta Coro, et al.
Tetrahedron Letters (2017) Vol. 58, Iss. 18, pp. 1784-1787
Closed Access | Times Cited: 10
Toward solid-phase peptide fragment ligation by a traceless-Ugi multicomponent reaction approach
Steve Jobin, Alexia Méjean, Sindy-Marcela Galindo, et al.
Organic & Biomolecular Chemistry (2016) Vol. 14, Iss. 47, pp. 11230-11237
Open Access | Times Cited: 9
An Efficient One‐Pot Synthesis of Chiral N‐Protected 3‐Substituted (Diketo)piperazines via Ugi‐4CR/De‐Boc/Cyclization Process
Mouhamad Jida, Steven Ballet
ChemistrySelect (2018) Vol. 3, Iss. 4, pp. 1027-1031
Closed Access | Times Cited: 9
Synthesis of Peptide N-Acylpyrroles via Anodically Generated N,O-Acetals
Lara R. Malins, Yutong Lin
Synthesis (2022) Vol. 54, Iss. 16, pp. 3558-3567
Open Access | Times Cited: 5
Methionine and seleno-methionine type peptide and peptoid building blocks synthesized by five-component five-center reactions
Goran N. Kaluđerović, Muhammad Abbas, Hans Christian Kautz, et al.
Chemical Communications (2017) Vol. 53, Iss. 26, pp. 3777-3780
Closed Access | Times Cited: 7
Facile construction of peptidomimetics by sequential C–S/C–N bond activation of Ugi-adducts
Chao Liu, Liangliang Song, Vsevolod A. Peshkov, et al.
Organic Chemistry Frontiers (2021) Vol. 8, Iss. 24, pp. 6968-6973
Open Access | Times Cited: 4
Macrocycles from Multicomponent Reactions
Ludger A. Wessjohann, Ricardo A. W. Neves Filho, Alfredo R. Puentes, et al.
(2017), pp. 339-376
Closed Access | Times Cited: 3
Amide‐Forming Ligation Reactions
Vijaya R. Pattabiraman, Ayodele O. Ogunkoya, Jeffrey W. Bode
Organic reactions (2019), pp. 231-592
Closed Access | Times Cited: 2
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