A. F. Bernardini

726 total citations
26 papers, 597 citations indexed

About

A. F. Bernardini is a scholar working on Organic Chemistry, Food Science and Molecular Biology. According to data from OpenAlex, A. F. Bernardini has authored 26 papers receiving a total of 597 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Organic Chemistry, 9 papers in Food Science and 8 papers in Molecular Biology. Recurrent topics in A. F. Bernardini's work include Essential Oils and Antimicrobial Activity (9 papers), Synthesis and Characterization of Heterocyclic Compounds (7 papers) and Phytochemistry and Biological Activities (7 papers). A. F. Bernardini is often cited by papers focused on Essential Oils and Antimicrobial Activity (9 papers), Synthesis and Characterization of Heterocyclic Compounds (7 papers) and Phytochemistry and Biological Activities (7 papers). A. F. Bernardini collaborates with scholars based in France, Italy and Portugal. A. F. Bernardini's co-authors include Alain Muselli, Jean‐Michel Bolla, Jean‐Marie Pagès, Liliane Berti, Vannina Lorenzi, Leonard Amaral, Félix Tomi, Joseph Casanova, José Galberto Martins da Costa and Pascale Bradesi and has published in prestigious journals such as Antimicrobial Agents and Chemotherapy, Tetrahedron and Phytochemistry.

In The Last Decade

A. F. Bernardini

25 papers receiving 556 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
A. F. Bernardini France 11 359 295 205 87 54 26 597
B. Diallo Belgium 14 261 0.7× 283 1.0× 484 2.4× 40 0.5× 98 1.8× 28 948
Shane G. Griffin Australia 7 489 1.4× 324 1.1× 217 1.1× 63 0.7× 10 0.2× 7 758
Mirta Susana Demo Argentina 16 502 1.4× 395 1.3× 181 0.9× 64 0.7× 14 0.3× 30 771
Akiko Shiraishi Japan 11 289 0.8× 414 1.4× 407 2.0× 78 0.9× 18 0.3× 17 901
N Didry France 9 314 0.9× 366 1.2× 213 1.0× 48 0.6× 10 0.2× 14 675
Gina Porras United States 10 190 0.5× 162 0.5× 176 0.9× 82 0.9× 26 0.5× 15 633
Pavel Nový Czechia 16 292 0.8× 322 1.1× 225 1.1× 36 0.4× 28 0.5× 39 738
T. R. Santha Kumar India 13 245 0.7× 211 0.7× 239 1.2× 84 1.0× 10 0.2× 21 751
Ismail Shah Pakistan 16 159 0.4× 239 0.8× 193 0.9× 69 0.8× 23 0.4× 53 710
Jacqueline Cosmo Andrade Brazil 13 196 0.5× 220 0.7× 180 0.9× 31 0.4× 34 0.6× 59 535

Countries citing papers authored by A. F. Bernardini

Since Specialization
Citations

This map shows the geographic impact of A. F. Bernardini'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 A. F. Bernardini with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites A. F. Bernardini more than expected).

Fields of papers citing papers by A. F. Bernardini

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by A. F. Bernardini. 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 A. F. Bernardini. The network helps show where A. F. Bernardini may publish in the future.

Co-authorship network of co-authors of A. F. Bernardini

This figure shows the co-authorship network connecting the top 25 collaborators of A. F. Bernardini. A scholar is included among the top collaborators of A. F. Bernardini 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 A. F. Bernardini. A. F. Bernardini 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.
Viciani, Daniele, Giulio Ferretti, A. F. Bernardini, Mauro Raffaelli, & Lorenzo Lastrucci. (2020). An annotated checklist of the vascular flora of the Arezzo administrative province (Tuscany, Italy). Plant Biosystems - An International Journal Dealing with all Aspects of Plant Biology. 155(5). 971–982. 3 indexed citations
2.
Usaï, Marianna, Marzia Foddai, A. F. Bernardini, et al.. (2010). Chemical Composition and Variation of the Essential Oil of Wild SardinianHelichrysum ItalicumG. Don subsp.Microphyllum(Willd.) Nym from Vegetative Period to Post-blooming. Journal of Essential Oil Research. 22(5). 373–380. 29 indexed citations
3.
Leoni, Eric, Dominique Cancellieri, Pierre Tomi, et al.. (2003). Thermal Degradation of Pinus Pinaster Needles by DSC, Part 2: Kinetics of Exothermic Phenomena. Journal of Fire Sciences. 21(2). 117–130. 14 indexed citations
4.
Leoni, Eric, et al.. (2001). Thermal Degradation of Pinus pinaster Needles by DSC. Part 1: Dehydration Kinetics. Journal of Fire Sciences. 19(5). 379–397. 14 indexed citations
5.
Tomi, Félix, et al.. (1998). Composition and infraspecific variability of essential oil from Thymus herba barona Lois. Biochemical Systematics and Ecology. 26(8). 915–932. 33 indexed citations
6.
Casanova, Joseph, et al.. (1997). Composition of the Essential Oil ofCistus ladaniferus L. Cultivated in Corsica (France). Flavour and Fragrance Journal. 12(3). 147–151. 46 indexed citations
7.
Casanova, Joseph, et al.. (1997). Composition of the Essential Oil of Cistus ladaniferus L. Cultivated in Corsica (France). Flavour and Fragrance Journal. 12(3). 147–151.
8.
Bernardini, A. F., et al.. (1995). Free flavonoid aglycones from Thymus herba barona and its monoterpenoid chemotypes. Phytochemistry. 40(1). 115–120. 33 indexed citations
9.
Essassi, El Mokhtar, et al.. (1983). Etude de la réaction de l'acétylacétone avec les diamines hétéroaromatiques. Journal of Heterocyclic Chemistry. 20(4). 1015–1018. 8 indexed citations
10.
Bernardini, A. F., et al.. (1983). Utilisation des organocuprates a la synthese d'aminoacides. Tetrahedron Letters. 24(35). 3717–3720. 10 indexed citations
11.
Bernardini, A. F., et al.. (1982). 13C NMR spectra of benzodiazepinones: Application to isomeric structure determination. Organic Magnetic Resonance. 18(3). 134–137. 6 indexed citations
12.
Bernardini, A. F., Philippe Viallefont, & René Milcent. (1979). Fragmentation sous l'Impact Electronique d'Amino‐4 triazole‐1,2,4 ones‐5. Organic Mass Spectrometry. 14(7). 369–378. 3 indexed citations
13.
Bernardini, A. F., et al.. (1978). Fragmentation sous l'Impact Electronique de Bitriazoles‐5(3),1′ et de Bitriazoles‐4,4′. Organic Mass Spectrometry. 13(2). 74–80. 3 indexed citations
14.
Bernardini, A. F., et al.. (1978). Etude de la réaction de l'acé'tylacé'tate d'éthyle avec les diamino‐1,5 imidazoles. Journal of Heterocyclic Chemistry. 15(6). 937–944. 6 indexed citations
15.
Maury, Georges, et al.. (1977). Etude expérimentale et théorique de la substitution de N‐méthyl‐halogéno‐triazoles‐1,2,4 par les réactifs nucléophiles. Journal of Heterocyclic Chemistry. 14(8). 1311–1315. 1 indexed citations
16.
Bernardini, A. F., et al.. (1977). Synthéses de bitriazoles‐3(‐5),1′ méthylés en position 1 ou 4 et de bitriazoles‐4,4′. Journal of Heterocyclic Chemistry. 14(3). 397–400. 5 indexed citations
17.
Bernardini, A. F., et al.. (1977). Fragmentation sous l'Impact Electronique de Diamino‐4,5 Triazoles‐1,2,4 et d'Amino‐4 Mercapto‐5 Triazoles‐1,2,4. Organic Mass Spectrometry. 12(10). 638–643. 4 indexed citations
18.
Bernardini, A. F., et al.. (1976). Étude de la tautomérie des halogéno-triazoles-1,2,4 par determination expérimentale et théorique de leurs moments dipolaires. Journal of Molecular Structure. 34(2). 245–262. 5 indexed citations
19.
Bernardini, A. F., Philippe Viallefont, & Jacques Daunis. (1975). Determination de la structure d'halogenotriazoles‐1,2,4 par spectrometrie de masse. Journal of Heterocyclic Chemistry. 12(4). 655–659. 15 indexed citations
20.
Pappalardo, Giuseppe, et al.. (1967). [Relationship between structure and antibacterial activity of arylthioamides. II. Antibacterial activity, UV and IR spectra, acid hydrolysis of aryl- and arylvinylenethioamides].. PubMed. 22(10). 808–20. 1 indexed citations

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