Jean‐Bernard Ducep

851 total citations
36 papers, 644 citations indexed

About

Jean‐Bernard Ducep is a scholar working on Organic Chemistry, Molecular Biology and Pharmaceutical Science. According to data from OpenAlex, Jean‐Bernard Ducep has authored 36 papers receiving a total of 644 indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Organic Chemistry, 18 papers in Molecular Biology and 4 papers in Pharmaceutical Science. Recurrent topics in Jean‐Bernard Ducep's work include Chemical Synthesis and Analysis (9 papers), Chemical Synthesis and Reactions (7 papers) and Asymmetric Synthesis and Catalysis (6 papers). Jean‐Bernard Ducep is often cited by papers focused on Chemical Synthesis and Analysis (9 papers), Chemical Synthesis and Reactions (7 papers) and Asymmetric Synthesis and Catalysis (6 papers). Jean‐Bernard Ducep collaborates with scholars based in France and Canada. Jean‐Bernard Ducep's co-authors include J.F. Biellmann, Paul V. Attwood, Charles Danzin, Saul Wolfe, F. Gerhart, Chantal Tardif, William Higgins, Keith Robinson, François Piriou and Philip R. Kastner and has published in prestigious journals such as Diabetes, Biochemical Journal and Journal of Medicinal Chemistry.

In The Last Decade

Jean‐Bernard Ducep

36 papers receiving 592 citations

Peers

Jean‐Bernard Ducep

PHARM

BIOTE

P. D. WOODGATE New Zealand

John J. Partridge United States

Eiji Ohki United Kingdom

Poul Rasmussen Denmark

R. Bognár Hungary

José A. Salazar Spain

Toshiko Watanabe Japan

Girish K. Trivedi India

Ewart R. H. Jones United States

M. B. M. DE AZEVEDO Brazil

P. D. WOODGATE New Zealand

Jean‐Bernard Ducep

378 ×0.9

299 ×1.0

69 ×1.1

PHARM

64 ×1.1

40 ×1.0

BIOTE

Citations per year, relative to Jean‐Bernard Ducep Jean‐Bernard Ducep (= 1×) peers P. D. WOODGATE

Countries citing papers authored by Jean‐Bernard Ducep

Since Specialization

Citations

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

Fields of papers citing papers by Jean‐Bernard Ducep

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jean‐Bernard Ducep. 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 Jean‐Bernard Ducep. The network helps show where Jean‐Bernard Ducep may publish in the future.

Co-authorship network of co-authors of Jean‐Bernard Ducep

This figure shows the co-authorship network connecting the top 25 collaborators of Jean‐Bernard Ducep. A scholar is included among the top collaborators of Jean‐Bernard Ducep 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 Jean‐Bernard Ducep. Jean‐Bernard Ducep 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

George, Pascal, et al.. (2003). Polymer-supported electron-rich diene for hetero Diels–Alder reactions. Tetrahedron Letters. 44(18). 3645–3647. 20 indexed citations

Ducep, Jean‐Bernard, et al.. (1997). Synthesis of (2S,5S)-5-fluoromethylornithine; a potent inhibitor of ornithine aminotransferase. Tetrahedron Asymmetry. 8(2). 327–335. 8 indexed citations

Piettre, Serge R., Catherine André, Jean‐Bernard Ducep, et al.. (1997). Monoaryl- and Bisaryldihydroxytropolones as Potent Inhibitors of Inositol Monophosphatase. Journal of Medicinal Chemistry. 40(26). 4208–4221. 44 indexed citations

Ducep, Jean‐Bernard, et al.. (1996). Synthesis of 5,6-difluoroarachidonic acid, a potential inhibitor of 5-lipoxygenase. Tetrahedron Letters. 37(28). 4941–4944. 6 indexed citations

Ducep, Jean‐Bernard, et al.. (1994). Synthesis of 5- and 6-fluoro derivatives of 5,8,14-eicosatrienoic and 5,8,11,14-eicosatetraenoic acids. Effects of fluorinated arachidonic acids on leukotriene C4 production by macrophages. Bioorganic & Medicinal Chemistry. 2(3). 213–233. 3 indexed citations

Schirlin, Daniel, Jean‐Bernard Ducep, Philippe Bey, et al.. (1992). Synthesis and inhibitory properties of α(chlorofluoromethyl)-α-amino acids, a novel class of irreversible inactivators of decarboxylases. Journal of the Chemical Society Perkin Transactions 1. 1053–1064. 11 indexed citations

Ducep, Jean‐Bernard, et al.. (1991). Evaluation of 5- and 6-fluoro derivatives of arachidonic acid and 5,8,14-eicosatrienoic acid as substrates and inhibitors of 5-lipoxygenase. Biochemical Journal. 278(2). 549–555. 3 indexed citations

Robinson, Keith, et al.. (1991). New Potent α-Glucohydrolase Inhibitor MDL 73945 With Long Duration of Action in Rats. Diabetes. 40(7). 825–830. 103 indexed citations

Gerhart, F., William Higgins, Chantal Tardif, & Jean‐Bernard Ducep. (1990). 2-(4-Amino-4-carboxybutyl)aziridine-2-carboxylic acid. A potent irreversible inhibitor of diaminopimelic acid epimerase. Spontaneous formation from .alpha.-(halomethyl)diaminopimelic acids. Journal of Medicinal Chemistry. 33(8). 2157–2162. 55 indexed citations

10.

Ducep, Jean‐Bernard, et al.. (1988). Use of simplified substrates for the study of 5-lipoxygenase from RBL-1 cells. Prostaglandins. 36(3). 385–398. 8 indexed citations

11.

Attwood, Paul V., et al.. (1988). Purification and properties of myo-inositol-1-phosphatase from bovine brain. Biochemical Journal. 253(2). 387–394. 57 indexed citations

12.

d'Orchymont, Hugues, et al.. (1985). Mechanism of the inhibition of cholesterol biosynthesis by 6-fluoromevalonate. Biochemical Journal. 227(1). 247–254. 39 indexed citations

13.

Bey, Philippe, Jean‐Bernard Ducep, & Daniel Schirlin. (1984). Alkylation of malonates or schiff base anions with dichlorofluoromethane as a route to α-chlorofluoromethyl or α-fluoromethyl α-amino acids. Tetrahedron Letters. 25(49). 5657–5660. 12 indexed citations

14.

Biellmann, J.F., Jean‐Bernard Ducep, & Daniel Schirlin. (1980). Rearrangements of the carbanions derived from allyl benzyl thioether. Tetrahedron. 36(9). 1249–1259. 12 indexed citations

15.

Biellmann, J.F., et al.. (1976). Thiophilic reaction of t-butyllithium on cyclic thioethers. Tetrahedron. 32(9). 1061–1064. 6 indexed citations

16.

Biellmann, J.F., et al.. (1976). Rearrangement of carbanions and of ylides derived from 4-thiacyclohexenyl systems. Tetrahedron. 32(14). 1801–1805. 23 indexed citations

17.

Wolfe, Saul, et al.. (1975). Sulfur-Free Penicillin Derivatives. V. Preparation, Hydrolysis, and Oxidative Rearrangement Of Fused Oxazoline–Azetidinones. Canadian Journal of Chemistry. 53(4). 497–512. 5 indexed citations

18.

Wolfe, Saul, et al.. (1972). Sulfur-free Penicillin Derivatives. II. Functionalization of the Methyl Groups. Canadian Journal of Chemistry. 50(17). 2898–2902. 6 indexed citations

19.

Biellmann, J.F. & Jean‐Bernard Ducep. (1971). Réarrangements sigmatropiques de carbanions dérivant de sulfures allyliques. Tetrahedron Letters. 12(1). 33–36. 10 indexed citations

20.

Biellmann, J.F. & Jean‐Bernard Ducep. (1969). Synthese du squalene par couplage queue a queue. Tetrahedron Letters. 10(42). 3707–3710. 24 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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