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:

Expedient entry to the piperazinohydroisoquinoline ring system using a sequential Ugi/Pictet–Spengler/reductive methylation reaction protocol
Ma.‐Angeles Cano‐Herrera, Luis D. Miranda
Chemical Communications (2011) Vol. 47, Iss. 38, pp. 10770-10770
Closed Access | Times Cited: 31

Showing 1-25 of 31 citing articles:

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

Two-Step Synthesis of 2,3-Dihydropyrroles via a Formal 5-endo Cycloisomerization of Ugi 4-CR/Propargyl Adducts
Luis A. Polindara‐García, Luis D. Miranda
Organic Letters (2012) Vol. 14, Iss. 21, pp. 5408-5411
Closed Access | Times Cited: 69

Highly Stereoselective Synthesis of Natural‐Product‐Like Hybrids by an Organocatalytic/Multicomponent Reaction Sequence
Radell Echemendía, Alexander F. de la Torre, Júlia L. Monteiro, et al.
Angewandte Chemie International Edition (2015) Vol. 54, Iss. 26, pp. 7621-7625
Closed Access | Times Cited: 52

A chemoselective Ugi-type reaction in water using TMSCN as a functional isonitrile equivalent: generation of heteroaromatic molecular diversity
Sankar K. Guchhait, Vikas Chaudhary, Chetna Madaan
Organic & Biomolecular Chemistry (2012) Vol. 10, Iss. 46, pp. 9271-9271
Closed Access | Times Cited: 44

Various cyclization scaffolds by a truly Ugi 4-CR
Mantosh K. Sinha, Kareem Khoury, Eberhardt Herdtweck, et al.
Organic & Biomolecular Chemistry (2013) Vol. 11, Iss. 29, pp. 4792-4792
Open Access | Times Cited: 39

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

Recent advances in the development of polycyclic skeletons via Ugi reaction cascades
Jie Lei, Jiang Ping Meng, Dianyong Tang, et al.
Molecular Diversity (2018) Vol. 22, Iss. 2, pp. 503-516
Closed Access | Times Cited: 31

Efficient synthesis of conformationally constrained, amino-triazoloazepinone-containing di- and tripeptides via a one-pot Ugi–Huisgen tandem reaction
Thomas Barlow, Mouhamad Jida, Dirk Tourwé, et al.
Organic & Biomolecular Chemistry (2014) Vol. 12, Iss. 36, pp. 6986-6989
Closed Access | Times Cited: 30

Asymmetric Synthesis of Bridged N-Heterocycles with Tertiary Carbon Center through Barbas Dienamine-Catalysis: Scope and Applications
Jyothi Yadav, Atul Jankiram Dolas, Eldhose Iype, et al.
The Journal of Organic Chemistry (2021) Vol. 86, Iss. 23, pp. 17213-17225
Closed Access | Times Cited: 21

An acid-promoted novel skeletal rearrangement initiated by intramolecular ipso-Friedel–Crafts-type addition to 3-alkylidene indolenium cations
Takuya Yokosaka, Tetsuhiro Nemoto, Yasumasa Hamada
Chemical Communications (2012) Vol. 48, Iss. 44, pp. 5431-5431
Closed Access | Times Cited: 28

Synthesis of novel tryptamine-based macrocycles using an Ugi 4-CR/microwave assisted click-cycloaddition reaction protocol
Lizbeth Chavez‐Acevedo, Luis D. Miranda
Organic & Biomolecular Chemistry (2015) Vol. 13, Iss. 15, pp. 4408-4412
Closed Access | Times Cited: 28

Multicomponent/Palladium-Catalyzed Cascade Entry to Benzopyrrolizidine Derivatives: Synthesis and Antioxidant Evaluation
Luis D. Miranda, Eduardo Hernández‐Vázquez
The Journal of Organic Chemistry (2015) Vol. 80, Iss. 21, pp. 10611-10623
Closed Access | Times Cited: 27

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

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 indolo[3,3a-c]isoquinolin-3,6-diones: formal synthesis of (±)-plicamine
Marco V. Mijangos, Luis D. Miranda
Organic & Biomolecular Chemistry (2016) Vol. 14, Iss. 15, pp. 3677-3680
Closed Access | Times Cited: 21

Facile synthesis of 2-(2-arylpyrrolidin-1-yl)pyrimidines via acid-catalyzed reaction of N-(4,4-diethoxybutyl)pyrimidin-2-amine with phenols
Almir S. Gazizov, N. I. Kharitonova, Аndrey V. Smolobochkin, et al.
Monatshefte für Chemie - Chemical Monthly (2015) Vol. 146, Iss. 11, pp. 1845-1849
Closed Access | Times Cited: 20

Highly stereoselective one-pot construction of trisubstituted tetrahydro-β-carboline-fused diketopiperazines: a synthetic route towards cialis analogues
Mouhamad Jida, Dirk Tourwé, Steven Ballet
RSC Advances (2014) Vol. 4, Iss. 72, pp. 38159-38163
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

Highly efficient construction of a bridged pentacyclic skeleton via a six-component domino reaction under microwave irradiation
Lei Fu, Xian Feng, Juanjuan Zhang, et al.
Green Chemistry (2014) Vol. 17, Iss. 3, pp. 1535-1545
Closed Access | Times Cited: 13

Diversity-oriented reconstruction of primitive diketopiperazine-fused tetrahydro-β-carboline ring systems via Pictet–Spengler/Ugi-4CR/deprotection-cyclization reactions
Irfan Khan, Shahnawaz Khan, Vikas Tyagi, et al.
RSC Advances (2015) Vol. 5, Iss. 124, pp. 102713-102722
Closed 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

Highly Stereoselective Synthesis of Natural‐Product‐Like Hybrids by an Organocatalytic/Multicomponent Reaction Sequence
Radell Echemendía, Alexander F. de la Torre, Júlia L. Monteiro, et al.
Angewandte Chemie (2015) Vol. 127, Iss. 26, pp. 7731-7735
Closed Access | Times Cited: 10

Peptidomimetics II
William D. Lubell
Topics in heterocyclic chemistry (2016)
Closed Access | Times Cited: 6

Recent Advances in the Ugi Multicomponent Reactions
José Alemán, Silvia Cabrera, Cuauhtémoc Alvarado
(2015), pp. 247-282
Closed Access | Times Cited: 5

Selective synthesis of polyfunctionalized hydroisoquinoline derivatives via a three-component domino reaction
Juanjuan Zhang, Jundie Hu, Cheng‐Pao Cao, et al.
RSC Advances (2014) Vol. 4, Iss. 107, pp. 62457-62464
Closed Access | Times Cited: 5

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