Jean‐Charles Marié

771 total citations
16 papers, 315 citations indexed

About

Jean‐Charles Marié is a scholar working on Organic Chemistry, Molecular Biology and Epidemiology. According to data from OpenAlex, Jean‐Charles Marié has authored 16 papers receiving a total of 315 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Organic Chemistry, 8 papers in Molecular Biology and 3 papers in Epidemiology. Recurrent topics in Jean‐Charles Marié's work include Chemical Synthesis and Analysis (5 papers), Synthetic Organic Chemistry Methods (5 papers) and Asymmetric Synthesis and Catalysis (4 papers). Jean‐Charles Marié is often cited by papers focused on Chemical Synthesis and Analysis (5 papers), Synthetic Organic Chemistry Methods (5 papers) and Asymmetric Synthesis and Catalysis (4 papers). Jean‐Charles Marié collaborates with scholars based in United States, France and China. Jean‐Charles Marié's co-authors include Gregory K. Friestad, Amy M. Deveau, Lisa A. Marcaurelle, Sarathy Kesavan, Jun Qin, Jingqiang Wei, Damian W. Young, Christine Courillon, Max Malacrìa and Jeremy R. Duvall and has published in prestigious journals such as The Journal of Organic Chemistry, Organic Letters and European Journal of Organic Chemistry.

In The Last Decade

Jean‐Charles Marié

16 papers receiving 312 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Jean‐Charles Marié United States	9	268	131	47	29	15	16	315
Ted Judd United States	8	259 1.0×	99 0.8×	50 1.1×	30 1.0×	31 2.1×	10	369
Felix González-López de Turiso United States	10	271 1.0×	103 0.8×	27 0.6×	41 1.4×	19 1.3×	12	335
Harsh M. Gauniyal India	12	383 1.4×	142 1.1×	37 0.8×	17 0.6×	16 1.1×	16	420
Doug T. H. Chou Canada	8	330 1.2×	176 1.3×	41 0.9×	13 0.4×	8 0.5×	10	403
Salvatore Sanna Coccone Italy	11	159 0.6×	109 0.8×	37 0.8×	16 0.6×	41 2.7×	14	264
Sandeep R. Ghorpade India	10	235 0.9×	161 1.2×	21 0.4×	11 0.4×	8 0.5×	14	330
Debora Chiodi United States	5	130 0.5×	63 0.5×	41 0.9×	13 0.4×	19 1.3×	7	240
Biswajit Kalita India	10	288 1.1×	104 0.8×	30 0.6×	20 0.7×	8 0.5×	22	340
Marie‐Aude Hiebel France	16	673 2.5×	154 1.2×	22 0.5×	39 1.3×	11 0.7×	42	725
Salman Jabri United States	8	226 0.8×	98 0.7×	27 0.6×	18 0.6×	5 0.3×	12	322

Countries citing papers authored by Jean‐Charles Marié

Since Specialization

Citations

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

Fields of papers citing papers by Jean‐Charles Marié

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jean‐Charles Marié

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

All Works

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16 of 16 papers shown

Nagiec, M. Marek, Jeremy R. Duvall, Adam Skepner, et al.. (2018). Novel tricyclic glycal-basedTRIB1inducers that reprogram LDL metabolism in hepatic cells. MedChemComm. 9(11). 1831–1842. 5 indexed citations

Duvall, Jeremy R., Leanne L. Bedard, Adel M. Naylor-Olsen, et al.. (2017). Identification of Highly Specific Diversity-Oriented Synthesis-Derived Inhibitors of Clostridium difficile. ACS Infectious Diseases. 3(5). 349–359. 16 indexed citations

Friestad, Gregory K., et al.. (2016). Stereoselective access to tubuphenylalanine and tubuvaline: improved Mn-mediated radical additions and assembly of a tubulysin tetrapeptide analog. The Journal of Antibiotics. 69(4). 294–298. 8 indexed citations

Dandapani, Sivaraman, Andrew Germain, Jean‐Charles Marié, et al.. (2013). Diversity-Oriented Synthesis Yields a New Drug Lead for Treatment of Chagas Disease. ACS Medicinal Chemistry Letters. 5(2). 149–153. 35 indexed citations

Carmody, Leigh, Andrew Germain, Juan C. Engel, et al.. (2013). Identification of Diversity-Oriented Synthesis Derived Small Molecule, ML341, with Cidal Activity Against Trypanosoma cruzi. 2 indexed citations

Gerard, Baudouin, Maurice D. Lee, Sivaraman Dandapani, et al.. (2013). Synthesis of Stereochemically and Skeletally Diverse Fused Ring Systems from Functionalized C-Glycosides. The Journal of Organic Chemistry. 78(11). 5160–5171. 15 indexed citations

Gerard, Baudouin, Jean‐Charles Marié, Bhaumik A. Pandya, et al.. (2011). Large-Scale Synthesis of All Stereoisomers of a 2,3-Unsaturated C-Glycoside Scaffold. The Journal of Organic Chemistry. 76(6). 1898–1901. 16 indexed citations

Marié, Jean‐Charles, Yuan Xiong, Geanna K. Min, et al.. (2010). Enantioselective Synthesis of 3,4-Chromanediones via Asymmetric Rearrangement of 3-Allyloxyflavones. The Journal of Organic Chemistry. 75(13). 4584–4590. 29 indexed citations

Wei, Jingqiang, et al.. (2009). Accessing Skeletal Diversity Using Catalyst Control: Formation of n and n + 1 Macrocyclic Triazole Rings. Organic Letters. 11(11). 2257–2260. 62 indexed citations

10.

Marié, Jean‐Charles, Christine Courillon, & Max Malacrìa. (2007). Selective ring opening of silylated vinyloxiranes and reactivity of azido-alcohols. ARKIVOC. 2007(5). 277–292. 3 indexed citations

11.

Friestad, Gregory K., et al.. (2006). Mn-Mediated Coupling of Alkyl Iodides and Chiral N-Acylhydrazones: Optimization, Scope, and Evidence for a Radical Mechanism. The Journal of Organic Chemistry. 71(18). 7016–7027. 35 indexed citations

12.

Marion, Frédéric, et al.. (2005). Silylated Vinyloxiranes – Recent Advances and Synthetic Applications. European Journal of Organic Chemistry. 2006(2). 453–462. 7 indexed citations

13.

Marié, Jean‐Charles, Christine Courillon, & Max Malacrìa. (2005). S_N2′ Reactions between Lithiated Carbon Nucleophiles and Silylated Vinyloxiranes – Effects of Salts and Solvents on the Stereocontrol. European Journal of Organic Chemistry. 2006(2). 463–470. 2 indexed citations

14.

Friestad, Gregory K., Jean‐Charles Marié, & Amy M. Deveau. (2004). Stereoselective Mn-Mediated Coupling of Functionalized Iodides and Hydrazones: A Synthetic Entry to the Tubulysin γ-Amino Acids. Organic Letters. 6(19). 3249–3252. 68 indexed citations

15.

Friestad, Gregory K., Jean‐Charles Marié, & Amy M. Deveau. (2004). Stereoselective Mn‐Mediated Coupling of Functionalized Iodides and Hydrazones: A Synthetic Entry to the Tubulysin α‐Amino Acids.. ChemInform. 36(2). 1 indexed citations

16.

Marié, Jean‐Charles, Christine Courillon, & Max Malacrìa. (2002). Compared Behaviors of trans- and cis-α,β-Epoxy-γ,δ-vinyl-silanes Towards Nucleophiles and Bases: High Regioselective Ring Opening and Deprotonation. Synlett. 2002(4). 553–556. 11 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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