Bruno Radatus

1.1k total citations
36 papers, 893 citations indexed

About

Bruno Radatus is a scholar working on Organic Chemistry, Molecular Biology and Epidemiology. According to data from OpenAlex, Bruno Radatus has authored 36 papers receiving a total of 893 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Organic Chemistry, 17 papers in Molecular Biology and 6 papers in Epidemiology. Recurrent topics in Bruno Radatus's work include Carbohydrate Chemistry and Synthesis (17 papers), Cyclopropane Reaction Mechanisms (7 papers) and Glycosylation and Glycoproteins Research (5 papers). Bruno Radatus is often cited by papers focused on Carbohydrate Chemistry and Synthesis (17 papers), Cyclopropane Reaction Mechanisms (7 papers) and Glycosylation and Glycoproteins Research (5 papers). Bruno Radatus collaborates with scholars based in Canada, United States and India. Bruno Radatus's co-authors include Kendall O. Smith, Karen S. Galloway, Kelvin K. Ogilvie, Bert Fraser‐Reid, W L Kennell, Mahmoud Mirmehrabi, K. S. K. MURTHY, Sohrab Rohani, Hans H. Baer and Michael F. Gillen and has published in prestigious journals such as Journal of the American Chemical Society, Antimicrobial Agents and Chemotherapy and Tetrahedron.

In The Last Decade

Bruno Radatus

36 papers receiving 781 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Bruno Radatus Canada 14 432 380 197 160 112 36 893
Stanley A. Lang United States 18 577 1.3× 362 1.0× 169 0.9× 118 0.7× 68 0.6× 52 1.2k
Alexander Hampton United States 21 421 1.0× 987 2.6× 173 0.9× 227 1.4× 64 0.6× 82 1.3k
Krystyna Lesiak United States 23 304 0.7× 865 2.3× 179 0.9× 315 2.0× 48 0.4× 67 1.3k
Christiane Yoakim Canada 28 1.1k 2.5× 624 1.6× 201 1.0× 306 1.9× 59 0.5× 51 1.8k
Keith G. Watson Australia 20 556 1.3× 467 1.2× 217 1.1× 105 0.7× 54 0.5× 53 1.2k
Thomas I. Kalman United States 16 278 0.6× 523 1.4× 94 0.5× 168 1.1× 77 0.7× 67 797
Benjamin A. Horenstein United States 19 443 1.0× 821 2.2× 132 0.7× 108 0.7× 123 1.1× 32 1.1k
Yoshihisa Mizuno Japan 16 527 1.2× 557 1.5× 77 0.4× 142 0.9× 37 0.3× 125 970
Christian Hubschwerlen Switzerland 21 621 1.4× 682 1.8× 175 0.9× 179 1.1× 92 0.8× 38 1.6k
H. Jeanette Thomas United States 20 479 1.1× 865 2.3× 178 0.9× 285 1.8× 25 0.2× 69 1.2k

Countries citing papers authored by Bruno Radatus

Since Specialization
Citations

This map shows the geographic impact of Bruno Radatus's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Bruno Radatus with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Bruno Radatus more than expected).

Fields of papers citing papers by Bruno Radatus

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Bruno Radatus. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Bruno Radatus. The network helps show where Bruno Radatus may publish in the future.

Co-authorship network of co-authors of Bruno Radatus

This figure shows the co-authorship network connecting the top 25 collaborators of Bruno Radatus. A scholar is included among the top collaborators of Bruno Radatus based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Bruno Radatus. Bruno Radatus is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Mirmehrabi, Mahmoud, Sohrab Rohani, K. S. K. MURTHY, & Bruno Radatus. (2004). Solubility, dissolution rate and phase transition studies of ranitidine hydrochloride tautomeric forms. International Journal of Pharmaceutics. 282(1-2). 73–85. 60 indexed citations
2.
Mirmehrabi, Mahmoud, Sohrab Rohani, K. S. K. MURTHY, & Bruno Radatus. (2004). Improving the filterability and solid density of ranitidine hydrochloride form 1. Journal of Pharmaceutical Sciences. 93(7). 1692–1700. 13 indexed citations
3.
Mirmehrabi, Mahmoud, Sohrab Rohani, K. S. K. MURTHY, & Bruno Radatus. (2003). Characterization of tautomeric forms of ranitidine hydrochloride: thermal analysis, solid-state NMR, X-ray. Journal of Crystal Growth. 260(3-4). 517–526. 62 indexed citations
4.
Mirzayans, Razmik, et al.. (1994). Comparative genotoxicity of 2,3'-O-cyclocytidine, β-xylocytidine and 1-β-D-arabinofuranosylcytosine in human tumor cell lines. Carcinogenesis. 15(10). 2319–2324. 2 indexed citations
5.
6.
Baer, Hans H., Ursula J. Williams, & Bruno Radatus. (1988). Nucleophilic ring-opening in a carbohydrate nitrocyclopropane: A stereospecific approach to chiral isoalkyl structures. Carbohydrate Research. 174. 291–303. 7 indexed citations
7.
8.
9.
Ogilvie, Kelvin K., et al.. (1984). Uracil analogues of the acyclonucleoside 9-[[2-hydroxy-1-(hydroxymethyl)ethoxy]- methyl]guanine (BIOLF-62). Canadian Journal of Chemistry. 62(1). 16–21. 47 indexed citations
10.
Baer, Hans H. & Bruno Radatus. (1984). Preparation of some partially protected, α,α-trehalose-type disaccharides having the d-altro configuration. Carbohydrate Research. 128(1). 165–174. 27 indexed citations
11.
Ogilvie, Kelvin K., et al.. (1983). Synthesis of 5-Substituted-1-[[2-Hydroxy-1-(hydroxymethyl)ethoxy]methyl]cytosines. Nucleosides and Nucleotides. 2(2). 147–154. 11 indexed citations
12.
Smith, Kendall O., Karen S. Galloway, Sara D. Hodges, et al.. (1983). Sensitivity of equine herpesviruses 1 and 3 in vitro to a new nucleoside analogue, 9-[[2-hydroxy-1-(hydroxymethyl) ethoxy] methyl] guanine. American Journal of Veterinary Research. 44(6). 1032–1035. 24 indexed citations
13.
Ogilvie, Kelvin K., et al.. (1982). Biologically active acyclonucleoside analogues. II. The synthesis of 9-[[2-hydroxy-1-(hydroxymethyl)ethoxy]methyl]guanine (BIOLF-62). Canadian Journal of Chemistry. 60(24). 3005–3010. 92 indexed citations
14.
Fraser‐Reid, Bert, S. Y. K. TAM, & Bruno Radatus. (1975). Lithium Aluminum Hydride Reductive Rearrangement of Allylic Acetals to Vinyl Ethers: A Synthesis of 3-Deoxy Glycals. Canadian Journal of Chemistry. 53(13). 2005–2016. 33 indexed citations
15.
Reckendorf, Wolfgang Meyer Zu, et al.. (1974). Glycoside von Aminozuckern, IV. Synthese von Disacchariden der 2‐Amino‐2‐desoxy‐ und der 3‐Amino‐3‐desoxy‐D‐glucose. Chemische Berichte. 107(3). 869–875. 3 indexed citations
16.
Fraser‐Reid, Bert & Bruno Radatus. (1972). Cyclopropylcarbinyl-oxo-carbonium Ions. Part VI. Synthesis and Chemistry of an Epimeric Pair of Homoallyl Iodides (3-Iodomethyl Glycals). Canadian Journal of Chemistry. 50(18). 2919–2927. 9 indexed citations
17.
Radatus, Bruno & Bert Fraser‐Reid. (1972). Cyclopropylcarbinyl-oxo-carbonium Ions. Part V. Synthesis and Chemistry of some Cyclopropyl Glycopyranosides. Canadian Journal of Chemistry. 50(18). 2909–2918. 10 indexed citations
18.
Fraser‐Reid, Bert & Bruno Radatus. (1971). Stereochemistry of deoxygenation of ribonucleotides. Specifically 2'-monodeuterated 2'-deoxycytidines. Journal of the American Chemical Society. 93(23). 6342–6344. 19 indexed citations
19.
Fraser‐Reid, Bert & Bruno Radatus. (1970). 4,6-Di-O-acetyl-aldehydo-2,3-dideoxy-D-erythro-trans-hex-2-enose. Probable reason for the 'al' in Emil Fischer's triacetyl glucal. Journal of the American Chemical Society. 92(17). 5288–5290. 34 indexed citations
20.
Fraser‐Reid, Bert & Bruno Radatus. (1970). Cyclopropylcarbinyl-oxo-carboniumions. A solvolytic basis for the cyclopropylcarbinyl-oxo-carbonium ion. Canadian Journal of Chemistry. 48(13). 2146–2148. 10 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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