M. Madesclaire

917 total citations
36 papers, 734 citations indexed

About

M. Madesclaire is a scholar working on Organic Chemistry, Molecular Biology and Spectroscopy. According to data from OpenAlex, M. Madesclaire has authored 36 papers receiving a total of 734 indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Organic Chemistry, 11 papers in Molecular Biology and 6 papers in Spectroscopy. Recurrent topics in M. Madesclaire's work include Synthesis and Reactivity of Sulfur-Containing Compounds (8 papers), Synthesis and Characterization of Heterocyclic Compounds (6 papers) and Chemical Synthesis and Analysis (5 papers). M. Madesclaire is often cited by papers focused on Synthesis and Reactivity of Sulfur-Containing Compounds (8 papers), Synthesis and Characterization of Heterocyclic Compounds (6 papers) and Chemical Synthesis and Analysis (5 papers). M. Madesclaire collaborates with scholars based in France, Russia and New Zealand. M. Madesclaire's co-authors include Pascal Coudert, A. Fauve, André‐Paul Carnat, Jean‐Louis Lamaison, A. Carpy, Alain Gueiffier, Olivier Chavignon, Yves Blache, Claire Lartigue and Catherine Rubat and has published in prestigious journals such as The Journal of Organic Chemistry, Tetrahedron and European Journal of Medicinal Chemistry.

In The Last Decade

M. Madesclaire

26 papers receiving 701 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
M. Madesclaire France 11 535 154 81 79 44 36 734
Piotr Bałczewski Poland 15 538 1.0× 102 0.7× 56 0.7× 69 0.9× 38 0.9× 68 729
Derek Walker United States 10 448 0.8× 121 0.8× 64 0.8× 76 1.0× 43 1.0× 21 623
Г. А. Толстиков Russia 11 289 0.5× 186 1.2× 54 0.7× 51 0.6× 47 1.1× 112 546
T. R. KASTURI India 12 379 0.7× 144 0.9× 83 1.0× 50 0.6× 29 0.7× 73 646
Marek Koprowski Poland 16 466 0.9× 188 1.2× 46 0.6× 134 1.7× 32 0.7× 49 763
Adele Bolognese Italy 15 449 0.8× 208 1.4× 42 0.5× 27 0.3× 63 1.4× 34 697
Jie Ji China 18 668 1.2× 218 1.4× 64 0.8× 186 2.4× 35 0.8× 34 1.0k
Fang Tian China 22 984 1.8× 308 2.0× 82 1.0× 98 1.2× 40 0.9× 63 1.2k
Е. В. Суслов Russia 15 291 0.5× 245 1.6× 106 1.3× 137 1.7× 61 1.4× 66 592
Akella V. S. Sarma India 19 498 0.9× 377 2.4× 87 1.1× 56 0.7× 78 1.8× 61 870

Countries citing papers authored by M. Madesclaire

Since Specialization
Citations

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

Fields of papers citing papers by M. Madesclaire

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of M. Madesclaire

This figure shows the co-authorship network connecting the top 25 collaborators of M. Madesclaire. A scholar is included among the top collaborators of M. Madesclaire 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 M. Madesclaire. M. Madesclaire 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.
Madesclaire, M., et al.. (2015). Synthesis and Antimicrobial Activity of New Ureas from (1S,2S)-2-Amino-1-(4-Nitrophenyl)-1,3-Propanediol. Pharmaceutical Chemistry Journal. 49(1). 10–12. 5 indexed citations
2.
3.
Chezal, Jean‐Michel, et al.. (2011). Design, synthesis and in vitro drug release investigation of new potential 5-FU prodrugs. European Journal of Medicinal Chemistry. 46(7). 2867–2879. 18 indexed citations
4.
Madesclaire, M., et al.. (2011). An unexpected result from the reaction of hydroxymethyl-2-oxazolidinones with isocyanates. Chemistry of Heterocyclic Compounds. 47(2). 204–209.
5.
Coudert, Pascal, et al.. (2011). Synthesis and in vitro Studies of Pyrone Derivatives as Scavengers of Active Oxygen Species. PubMed. 51(11). 877–884. 2 indexed citations
6.
Galmier, Marie‐Josèphe, et al.. (2008). Synthesis and cytotoxic properties of new fluorodeoxyglucose-coupled chlorambucil derivatives. Bioorganic & Medicinal Chemistry. 16(9). 5004–5020. 37 indexed citations
7.
Madesclaire, M., et al.. (2007). Synthesis of isomeric 2-oxazolidinones from (1R,2R)-and (1S,2S)-2-amino-1-(4-nitrophenyl)-1,3-propanediols. Chemistry of Heterocyclic Compounds. 43(10). 1325–1332. 2 indexed citations
8.
Rubat, Catherine, et al.. (2005). New 3- and 4-hydroxyfuranones as anti-oxidants and anti-inflammatory agents. Bioorganic & Medicinal Chemistry. 13(14). 4552–4564. 52 indexed citations
9.
Galmier, Marie‐Josèphe, et al.. (2003). Nifuroxazide Photodecomposition: Identification of the (Z)-isomer by 1 H-NMR Study. Microchimica Acta. 141(3-4). 179–181. 4 indexed citations
10.
Madesclaire, M., et al.. (2002). Hydrazinolysis of Compounds Containing Oxazolidine Ring. Chemistry of Heterocyclic Compounds. 38(1). 71–73. 4 indexed citations
11.
COUQUELET, J., et al.. (2001). Synthesis and Stereochemistry of (1S,3S,4S,7R11R)-3-(4-Nitrophenyl)-11-aza-2,6-dioxatricyclo[5,3,1,04,11]undecane. Chemistry of Heterocyclic Compounds. 37(7). 898–902.
12.
13.
Madesclaire, M., et al.. (1996). (E)-3-(4-Chlorophenyl)-3-cyclopropyl-2-(phenylthio)acrylonitrile. Acta Crystallographica Section C Crystal Structure Communications. 52(12). 3104–3105.
14.
Gautier, Arnaud, et al.. (1995). Diastereoselective synthesis of ethyl (Z)-3-(8-methylimidazo-[1,2-a]pyrid-2-yl)-2-phenylthioacrylate. X-ray crystal structure and conformational analysis. Journal of Molecular Structure. 355(2). 177–183. 3 indexed citations
15.
Carnat, André‐Paul, et al.. (1992). cis-Chrysanthenol, A Main Component in Essential Oil ofArtemisia absinthiumL. Growing in Auvergne (Massif Central), France. Journal of Essential Oil Research. 4(5). 487–490. 43 indexed citations
16.
17.
Fauve, A., et al.. (1991). Microbial Oxidation of Vinyl Sulfides to Chiral sulfoxides. Biocatalysis. 4(4). 265–276. 5 indexed citations
18.
Gueiffier, Alain, Yves Blache, Olivier Chavignon, et al.. (1990). Synthesis of 1H-imidazo(1,2-a)pyrazolo(3,4-c)pyridines.. Chemical and Pharmaceutical Bulletin. 38(9). 2352–2356. 12 indexed citations
19.
Madesclaire, M., et al.. (1987). Stereoselective Synthesis of 2-Aryl-5-halo-2-pentenyl Methyl Sulfoxides and Sulfones. Synthesis. 1987(9). 834–835. 2 indexed citations
20.
Carpy, A., J.-M. Léger, A Boucherle, & M. Madesclaire. (1979). [Hydroxy-2 phényl-2 (pyridyl-2)-2 éthyl] méthyl sulfoxyde. Acta Crystallographica Section B. 35(11). 2566–2569.

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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