Damien Hazelard

1.3k total citations
31 papers, 1.1k citations indexed

About

Damien Hazelard is a scholar working on Organic Chemistry, Molecular Biology and Inorganic Chemistry. According to data from OpenAlex, Damien Hazelard has authored 31 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 31 papers in Organic Chemistry, 15 papers in Molecular Biology and 4 papers in Inorganic Chemistry. Recurrent topics in Damien Hazelard's work include Synthetic Organic Chemistry Methods (13 papers), Carbohydrate Chemistry and Synthesis (13 papers) and Chemical Synthesis and Analysis (10 papers). Damien Hazelard is often cited by papers focused on Synthetic Organic Chemistry Methods (13 papers), Carbohydrate Chemistry and Synthesis (13 papers) and Chemical Synthesis and Analysis (10 papers). Damien Hazelard collaborates with scholars based in France, Japan and Spain. Damien Hazelard's co-authors include Philippe Compain, Yujiro Hayashi, Seiji Aratake, Tsubasa Okano, Julien Iehl, Camille Decroocq, Jean‐François Nierengarten, Teresa Mena Barragán, Carmen Ortiz Mellet and Michel Holler and has published in prestigious journals such as Angewandte Chemie International Edition, SHILAP Revista de lepidopterología and The Journal of Organic Chemistry.

In The Last Decade

Damien Hazelard

31 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Damien Hazelard France 13 1.1k 375 159 63 53 31 1.1k
Valérie Desvergnes France 18 567 0.5× 313 0.8× 76 0.5× 47 0.7× 73 1.4× 36 759
Gabriel E. Job United States 10 842 0.8× 312 0.8× 125 0.8× 29 0.5× 69 1.3× 11 1.0k
Marı́a M. Zurbano Spain 18 664 0.6× 423 1.1× 113 0.7× 16 0.3× 129 2.4× 43 847
Hai‐Liang Zhu China 14 493 0.5× 359 1.0× 147 0.9× 55 0.9× 82 1.5× 55 807
Yousuke Yamaoka Japan 21 1.4k 1.3× 272 0.7× 285 1.8× 21 0.3× 103 1.9× 75 1.5k
Mark A. Lyster United States 9 683 0.6× 276 0.7× 91 0.6× 40 0.6× 69 1.3× 11 905
L. F. Kasukhin Russia 6 1.1k 1.1× 499 1.3× 277 1.7× 18 0.3× 51 1.0× 8 1.3k
Mathias Frederiksen United States 11 1.0k 1.0× 186 0.5× 318 2.0× 32 0.5× 17 0.3× 19 1.2k
Daniel Zewge United States 15 744 0.7× 337 0.9× 137 0.9× 12 0.2× 57 1.1× 28 1.0k
Mark McLaughlin United Kingdom 21 983 0.9× 205 0.5× 166 1.0× 71 1.1× 84 1.6× 52 1.1k

Countries citing papers authored by Damien Hazelard

Since Specialization
Citations

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

Fields of papers citing papers by Damien Hazelard

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Damien Hazelard

This figure shows the co-authorship network connecting the top 25 collaborators of Damien Hazelard. A scholar is included among the top collaborators of Damien Hazelard 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 Damien Hazelard. Damien Hazelard 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.
Yang, Zhongzhen, Damien Hazelard, Adrian C. Whitwood, et al.. (2024). Expanding the scope of the successive ring expansion strategy for macrocycle and medium-sized ring synthesis: unreactive and reactive lactams. Organic & Biomolecular Chemistry. 22(15). 2985–2991. 2 indexed citations
2.
Liu, Haijuan, et al.. (2022). Formal Glycosylation of Quinones with exo-Glycals Enabled by Iron-Mediated Oxidative Radical–Polar Crossover. The Journal of Organic Chemistry. 87(19). 13178–13194. 10 indexed citations
3.
Hazelard, Damien, et al.. (2019). Stereoselective Synthesis of C,C-Glycosides from exo-Glycals Enabled by Iron-Mediated Hydrogen Atom Transfer. Organic Letters. 21(18). 7262–7267. 38 indexed citations
4.
Kern, Nicolas, et al.. (2018). Stereocontrolled synthesis of polyhydroxylated bicyclic azetidines as a new class of iminosugars. Organic & Biomolecular Chemistry. 16(25). 4688–4700. 9 indexed citations
5.
Hazelard, Damien, et al.. (2018). One-Pot, Highly Stereoselective Synthesis of Dithioacetal-α,α-Diglycosides. Molecules. 23(4). 914–914. 7 indexed citations
6.
Hazelard, Damien, et al.. (2017). Catalytic C–H amination at its limits: challenges and solutions. Organic Chemistry Frontiers. 4(12). 2500–2521. 144 indexed citations
7.
Hazelard, Damien, Josefina Casas, Helen Michelakakis, et al.. (2016). Investigation of original multivalent iminosugars as pharmacological chaperones for the treatment of Gaucher disease. Carbohydrate Research. 429. 98–104. 22 indexed citations
8.
Wencel‐Delord, Joanna, et al.. (2016). Pushing the limits of catalytic C–H amination in polyoxygenated cyclobutanes. Organic & Biomolecular Chemistry. 14(9). 2780–2796. 10 indexed citations
9.
Compain, Philippe, et al.. (2016). A Convenient, Gram-Scale Synthesis of 1-Deoxymannojirimycin. Synthesis. 48(8). 1177–1180. 8 indexed citations
10.
Wencel‐Delord, Joanna, et al.. (2015). Synthesis of a new class of iminosugars based on constrained azaspirocyclic scaffolds by way of catalytic C–H amination. Organic & Biomolecular Chemistry. 13(35). 9176–9180. 11 indexed citations
11.
Hazelard, Damien, et al.. (2012). Diastereoselective synthesis of the C17–C30 fragment of amphidinol 3. Organic & Biomolecular Chemistry. 10(47). 9418–9418. 17 indexed citations
12.
Compain, Philippe, Camille Decroocq, Julien Iehl, et al.. (2010). Glycosidase Inhibition with Fullerene Iminosugar Balls: A Dramatic Multivalent Effect. Angewandte Chemie International Edition. 49(33). 5753–5756. 168 indexed citations
13.
Hazelard, Damien, Antoine Fadel, & Régis Guillot. (2008). First synthesis of enantiomerically pure (1S,2S)- and (1R,2R)-1,2-diaminocyclobutanecarboxylic acid–ornithine derivative–, from racemic 2-aminocyclobutanone. Tetrahedron Asymmetry. 19(17). 2063–2067. 6 indexed citations
14.
Hazelard, Damien, Hayato Ishikawa, Daisuke Hashizume, Hiroyuki Koshino, & Yujiro Hayashi. (2008). ChemInform Abstract: Proline‐Mediated Enantioselective Construction of Tetrahydropyrans via a Domino Aldol/Acetalization Reaction.. ChemInform. 39(35). 1 indexed citations
15.
Hayashi, Yujiro, Tsubasa Okano, Seiji Aratake, & Damien Hazelard. (2007). Diphenylprolinol Silyl Ether as a Catalyst in an Enantioselective, Catalytic, Tandem Michael/Henry Reaction for the Control of Four Stereocenters. Angewandte Chemie. 119(26). 5010–5013. 223 indexed citations
16.
Hayashi, Yujiro, et al.. (2007). Diphenylprolinol Silyl Ether as a Catalyst in an Enantioselective, Catalytic, Tandem Michael/Henry Reaction for the Control of Four Stereocenters. Angewandte Chemie International Edition. 46(26). 4922–4925. 226 indexed citations
17.
18.
Hazelard, Damien & Antoine Fadel. (2005). Synthesis of optically active (+)-2-benzyl-, (+)-2-octyl-, and (+)-2-tetradec-5′-enylcyclobutanones via metallated chiral imines or hydrazones. Tetrahedron Asymmetry. 16(12). 2067–2070. 12 indexed citations
19.
Hazelard, Damien, Antoine Fadel, & Georges Morgant. (2004). The first synthesis of both enantiomers of 2-hydroxycyclobutanone acetals by enzymatic transesterification: preparation of (R)-(+)-2-benzyloxycyclobutanone and its antipode. Tetrahedron Asymmetry. 15(11). 1711–1718. 6 indexed citations
20.

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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