Gérard Boyer

1.3k total citations
67 papers, 1.1k citations indexed

About

Gérard Boyer is a scholar working on Organic Chemistry, Molecular Biology and Spectroscopy. According to data from OpenAlex, Gérard Boyer has authored 67 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 41 papers in Organic Chemistry, 30 papers in Molecular Biology and 9 papers in Spectroscopy. Recurrent topics in Gérard Boyer's work include Synthesis and Biological Evaluation (13 papers), Cancer therapeutics and mechanisms (12 papers) and Phenothiazines and Benzothiazines Synthesis and Activities (12 papers). Gérard Boyer is often cited by papers focused on Synthesis and Biological Evaluation (13 papers), Cancer therapeutics and mechanisms (12 papers) and Phenothiazines and Benzothiazines Synthesis and Activities (12 papers). Gérard Boyer collaborates with scholars based in France, Spain and Algeria. Gérard Boyer's co-authors include José Elguero, Rosa M. Claramunt, Sandrine Alibert, Jean‐Marie Pagès, Jean‐Pierre Finet, Jean‐Pierre Galy, Jean‐Michel Bolla, Jacqueline Chevalier, Katarzyna Kieć‐Kononowicz and Alexey Yu. Fedorov and has published in prestigious journals such as Journal of the American Chemical Society, SHILAP Revista de lepidopterología and The Journal of Physical Chemistry.

In The Last Decade

Gérard Boyer

63 papers receiving 993 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Gérard Boyer France	17	604	308	121	98	87	67	1.1k
U. Urleb Slovenia	18	392 0.6×	579 1.9×	152 1.3×	66 0.7×	158 1.8×	103	1.3k
Federico Berti Italy	24	650 1.1×	857 2.8×	51 0.4×	167 1.7×	111 1.3×	105	1.8k
Frank J. Wolf United States	20	563 0.9×	632 2.1×	172 1.4×	129 1.3×	130 1.5×	58	1.8k
Isabelle Forfar France	16	1.0k 1.7×	348 1.1×	43 0.4×	60 0.6×	37 0.4×	47	1.5k
Jakob Magolan Canada	19	686 1.1×	355 1.2×	134 1.1×	40 0.4×	82 0.9×	46	1.4k
Mauro V. de Almeida Brazil	20	547 0.9×	340 1.1×	23 0.2×	67 0.7×	131 1.5×	68	1.2k
Jacques Barbe France	20	657 1.1×	600 1.9×	357 3.0×	49 0.5×	41 0.5×	74	1.5k
Dejan Opsenica Serbia	21	705 1.2×	369 1.2×	30 0.2×	96 1.0×	87 1.0×	50	1.3k
Yen‐Peng Ho Taiwan	23	364 0.6×	715 2.3×	98 0.8×	458 4.7×	192 2.2×	62	1.9k
Ben Bardsley United Kingdom	11	350 0.6×	415 1.3×	53 0.4×	198 2.0×	76 0.9×	23	831

Countries citing papers authored by Gérard Boyer

Since Specialization

Citations

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

Fields of papers citing papers by Gérard Boyer

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Gérard Boyer. 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 Gérard Boyer. The network helps show where Gérard Boyer may publish in the future.

Co-authorship network of co-authors of Gérard Boyer

This figure shows the co-authorship network connecting the top 25 collaborators of Gérard Boyer. A scholar is included among the top collaborators of Gérard Boyer 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 Gérard Boyer. Gérard Boyer is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Boyer, Gérard, et al.. (2024). Molecular determinant deciphering of MIC-guided RND efflux substrates in E. coli. SHILAP Revista de lepidopterología. 4. 3 indexed citations

Alibert, Sandrine, et al.. (2016). Multidrug efflux pumps and their role in antibiotic and antiseptic resistance: a pharmacodynamic perspective. Expert Opinion on Drug Metabolism & Toxicology. 13(3). 301–309. 39 indexed citations

Chevalier, Jacqueline, Jadwiga Handzlik, Ewa Szymańska, et al.. (2016). Efflux Pump Blockers in Gram-Negative Bacteria: The New Generation of Hydantoin Based-Modulators to Improve Antibiotic Activity. Frontiers in Microbiology. 7. 622–622. 17 indexed citations

Shock, Everett L., et al.. (2013). Thermodynamics of Organic Transformations in Hydrothermal Fluids. Reviews in Mineralogy and Geochemistry. 76(1). 311–350. 47 indexed citations

Bolla, Jean‐Michel, Sandrine Alibert, Jadwiga Handzlik, et al.. (2011). Strategies for bypassing the membrane barrier in multidrug resistant Gram‐negative bacteria. FEBS Letters. 585(11). 1682–1690. 193 indexed citations

Giorgio, Carole Di, et al.. (2011). Evaluation of the mutagenic/clastogenic potential of 3,6-di-substituted acridines targeted for anticancer chemotherapy. Food and Chemical Toxicology. 49(11). 2773–2779. 9 indexed citations

Giorgio, Carole Di, et al.. (2009). Photo-inducible cytotoxic and clastogenic activities of 3,6-di-substituted acridines obtained by acylation of proflavine. European Journal of Medicinal Chemistry. 44(6). 2459–2467. 22 indexed citations

Tintaru, Aura, et al.. (2008). Differentiation of heterocyclic regioisomers: a combined tandem mass spectrometry and computational study of N ‐acridin‐4‐ylbenzylamide and N ‐acridin‐2‐yl‐benzylamide. Rapid Communications in Mass Spectrometry. 22(5). 687–693. 4 indexed citations

Giorgio, Carole Di, et al.. (2007). Synthesis and antileishmanial activity of 6-mono-substituted and 3,6-di-substituted acridines obtained by acylation of proflavine. European Journal of Medicinal Chemistry. 42(10). 1277–1284. 57 indexed citations

10.

Boyer, Gérard, et al.. (2005). ¹H and ¹³C chemical shifts for acridines: part XIX. N,N′‐diacylproflavine derivatives. Magnetic Resonance in Chemistry. 43(12). 1077–1079. 2 indexed citations

11.

Boyer, Gérard, et al.. (2005). Arylboronic Acid-Lead Tetraacetate-Copper Diacetate: A One-Pot System for Copper-Catalyzed N-Arylation Under Neutral Conditions. Letters in Organic Chemistry. 2(5). 407–409. 1 indexed citations

12.

Boyer, Gérard, et al.. (2003). New Macrocycles derived from 4,5-diamino- and 4,5-dihydroxyacridin-9(10H)-ones. Heterocyclic Communications. 9(3). 265–270. 4 indexed citations

13.

Boyer, Gérard, et al.. (2001). SYNTHESIS, STRUCTURE AND REACTIVITY OF TRIPHENYLBISMUTH BIS(2-THIOPHENECARBOXYLATE). Main Group Metal Chemistry. 24(11). 767–774. 9 indexed citations

14.

Boyer, Gérard & J. Galy. (1998). (6-Methoxy-2-naphthyl)-6-aminobenzodioxane. Molecules. 3(8). M89–M89. 1 indexed citations

15.

Morel, Sandrine, et al.. (1996). A Synthesis of 9-Methoxy-1-Methyl-1H,6H-Pyrazolo[4,3-c]Carbazole. Synthetic Communications. 26(13). 2443–2447. 11 indexed citations

16.

Catalán, Javier, Juan Carlos del Valle, Rosa M. Claramunt, et al.. (1994). Acidity and Basicity of Indazole and its N-Methyl Derivatives in the Ground and in the Excited State. The Journal of Physical Chemistry. 98(41). 10606–10612. 63 indexed citations

17.

Begtrup, Mikael, Gérard Boyer, Pilar Cabildo, et al.. (1993). ChemInform Abstract: Carbon‐13 NMR of Pyrazoles. ChemInform. 24(29). 1 indexed citations

18.

Claramunt, Rosa M., Dionísia Sanz, Gérard Boyer, et al.. (1993). Experimental (¹³C and ¹⁵N NMR spectroscopy) and theoretical (6–31G) study of the protonation of N‐methylazoles and N‐methylbenzazoles. Magnetic Resonance in Chemistry. 31(9). 791–800. 33 indexed citations

19.

Jean‐Pierre, Hélène, et al.. (1989). Pathogenicity in two cases of Staphylococcus schleiferi, a recently described species. Journal of Clinical Microbiology. 27(9). 2110–2111. 22 indexed citations

20.

Jean‐Pierre, Hélène, et al.. (1988). [Course of the resistance of Staphylococcus aureus to pefloxacin. A study based on 782 strains isolated in 1985 and 1986].. PubMed. 36(8). 956–8. 1 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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