Georges Dewynter

778 total citations
45 papers, 675 citations indexed

About

Georges Dewynter is a scholar working on Organic Chemistry, Molecular Biology and Spectroscopy. According to data from OpenAlex, Georges Dewynter has authored 45 papers receiving a total of 675 indexed citations (citations by other indexed papers that have themselves been cited), including 42 papers in Organic Chemistry, 26 papers in Molecular Biology and 5 papers in Spectroscopy. Recurrent topics in Georges Dewynter's work include Synthesis and Catalytic Reactions (22 papers), Chemical Synthesis and Analysis (11 papers) and Sulfur-Based Synthesis Techniques (9 papers). Georges Dewynter is often cited by papers focused on Synthesis and Catalytic Reactions (22 papers), Chemical Synthesis and Analysis (11 papers) and Sulfur-Based Synthesis Techniques (9 papers). Georges Dewynter collaborates with scholars based in France, Algeria and Canada. Georges Dewynter's co-authors include Jean‐Louis Montero, Jean Martínez, Loı̈c Toupet, Nour‐Eddine Aouf, Isabelle Parrot, Jean‐Yves Winum, Véronique Barragan, Normand Voyer, Loı̈c Toupet and Jean‐Louis Imbach and has published in prestigious journals such as Angewandte Chemie International Edition, Tetrahedron and Organic Letters.

In The Last Decade

Georges Dewynter

44 papers receiving 659 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Georges Dewynter France 17 568 392 49 43 37 45 675
N. Narendra India 15 447 0.8× 319 0.8× 76 1.6× 48 1.1× 15 0.4× 45 579
Ph. Viallefont France 16 648 1.1× 378 1.0× 44 0.9× 21 0.5× 28 0.8× 79 742
Xiangfu Lan United States 15 843 1.5× 184 0.5× 81 1.7× 38 0.9× 20 0.5× 19 919
T. ITAYA Japan 14 424 0.7× 430 1.1× 38 0.8× 28 0.7× 28 0.8× 125 739
Thomas Godet France 8 387 0.7× 259 0.7× 31 0.6× 27 0.6× 29 0.8× 12 599
Vicente Ojea Spain 15 453 0.8× 206 0.5× 76 1.6× 29 0.7× 21 0.6× 45 505
George Varvounis Greece 15 528 0.9× 146 0.4× 35 0.7× 31 0.7× 22 0.6× 58 600
Emilia Naydenova Bulgaria 12 433 0.8× 187 0.5× 66 1.3× 79 1.8× 19 0.5× 59 599
Giorgio Martelli Italy 17 664 1.2× 173 0.4× 130 2.7× 28 0.7× 29 0.8× 45 741
Valérie Desvergnes France 18 567 1.0× 313 0.8× 76 1.6× 38 0.9× 20 0.5× 36 759

Countries citing papers authored by Georges Dewynter

Since Specialization
Citations

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

Fields of papers citing papers by Georges Dewynter

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Georges Dewynter

This figure shows the co-authorship network connecting the top 25 collaborators of Georges Dewynter. A scholar is included among the top collaborators of Georges Dewynter 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 Georges Dewynter. Georges Dewynter 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.
Lee, Arie van der, et al.. (2018). Synthesis of Diastereomeric Pyrrolidine Sulfamides via Anchimerically Assisted Nucleophilic Substitution Reactions. Letters in Organic Chemistry. 15(5). 352–358. 2 indexed citations
2.
Ávila-Ortíz, C.G., et al.. (2012). Solution-phase synthesis of novel seven-membered cyclic dipeptides containing α- and β-amino acids. Tetrahedron. 68(47). 9842–9852. 8 indexed citations
3.
Colacino, Evelina, et al.. (2012). Unprecedented directed oxidative cross-coupling of sulfahydantoins with aldehydes via a radical sulfonate–sulfinate conversion. New Journal of Chemistry. 36(8). 1560–1560. 2 indexed citations
4.
Coursindel, Thibault, Audrey Restouin, Georges Dewynter, et al.. (2010). Stereoselective ring contraction of 2,5-diketopiperazines: An innovative approach to the synthesis of promising bioactive 5-membered scaffolds. Bioorganic Chemistry. 38(5). 210–217. 24 indexed citations
5.
Lopez, Gérald, et al.. (2010). Cyclosulfamide as a chiral auxiliary: application to efficient asymmetric synthesis (alkylation/aldolization). Tetrahedron Asymmetry. 21(19). 2361–2366. 19 indexed citations
6.
Martínez, Jean, et al.. (2009). Regioselective and sequential reactivity of activated 2,5‐diketopiperazines. Journal of Peptide Science. 15(7). 474–478. 13 indexed citations
7.
Parrot, Isabelle, et al.. (2008). Transannular rearrangement of activated 2,5-diketopiperazines: a key route to original scaffolds. Organic & Biomolecular Chemistry. 6(21). 3989–3989. 24 indexed citations
8.
Parrot, Isabelle, et al.. (2007). Transannular Rearrangement of Activated Lactams: Stereoselective Synthesis of Substituted Pyrrolidine‐2,4‐diones from Diketopiperazines. Angewandte Chemie International Edition. 46(39). 7488–7490. 26 indexed citations
9.
Berredjem, Malika, et al.. (2006). Simple and efficient synthesis of new chiral N,N′‐sulfonyl bis‐oxazolidin‐2‐ones. Heteroatom Chemistry. 17(1). 61–65. 9 indexed citations
10.
Dewynter, Georges, et al.. (1997). Sulfonyl bis-N-oxazolidinone (SBO): A new versatile dielectrophile with sequential reactivity. Tetrahedron Letters. 38(50). 8691–8694. 10 indexed citations
11.
Dewynter, Georges, et al.. (1996). Synthesis of pseudonucleosides containing chiral sulfahydantoins as aglycone (II). Tetrahedron. 52(3). 993–1004. 32 indexed citations
12.
13.
Dewynter, Georges, et al.. (1996). A new family of potential oncostatics: 2-chloroethylnitrososulfamides (CENS)—I. Synthesis, structure, and pharmacological evaluation (preliminary results). Bioorganic & Medicinal Chemistry. 4(8). 1227–1235. 40 indexed citations
14.
Dewynter, Georges, et al.. (1996). ChemInform Abstract: Synthesis of Pseudonucleosides Containing Chiral Sulfahydantoins as Aglycone. Part 2.. ChemInform. 27(17). 1 indexed citations
15.
Dewynter, Georges, et al.. (1996). SYNTHESIS OF 2-CHLOROETHYLNITROSOSULFAMIDES (CENS) VIA A TRANSSULFAMOYLATION REACTION. Phosphorus, sulfur, and silicon and the related elements. 118(1). 39–47. 18 indexed citations
16.
Dewynter, Georges, et al.. (1995). Synthese de derives phosphonyles de l'acide aspartique inhibiteurs potentiels de l'atcase. Phosphorus, sulfur, and silicon and the related elements. 105(1-4). 129–144. 15 indexed citations
17.
Dewynter, Georges, et al.. (1994). 3′-C-phosphonates as nucleotides analogues synthesis starting from original C-phosphonosugars (in ribo- and deoxyribo- series). Tetrahedron. 50(28). 8427–8444. 15 indexed citations
18.
19.
Dewynter, Georges, et al.. (1991). SYNTHESE ET STRUCTURE DE CHLOROETHYLSULFONYL-ET SULFOXYLUREES DERIVEES DE L'ISOCYANATE DE CHLOROSULFONYLE. Phosphorus, sulfur, and silicon and the related elements. 61(3-4). 223–237. 3 indexed citations
20.
Montero, Jean‐Louis, et al.. (1983). Selective synthesis of sulfonylureas and carboxysulfamides a novel route to oxazolidinones.. Tetrahedron Letters. 24(30). 3091–3094. 21 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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