Sylvain Lectard

1.1k total citations
11 papers, 948 citations indexed

About

Sylvain Lectard is a scholar working on Organic Chemistry, Inorganic Chemistry and Pharmaceutical Science. According to data from OpenAlex, Sylvain Lectard has authored 11 papers receiving a total of 948 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Organic Chemistry, 5 papers in Inorganic Chemistry and 3 papers in Pharmaceutical Science. Recurrent topics in Sylvain Lectard's work include Catalytic C–H Functionalization Methods (7 papers), Synthesis and Catalytic Reactions (6 papers) and Asymmetric Synthesis and Catalysis (4 papers). Sylvain Lectard is often cited by papers focused on Catalytic C–H Functionalization Methods (7 papers), Synthesis and Catalytic Reactions (6 papers) and Asymmetric Synthesis and Catalysis (4 papers). Sylvain Lectard collaborates with scholars based in Japan and Canada. Sylvain Lectard's co-authors include H. Lebel, Mikiko Sodeoka, Yoshitaka Hamashima, Kim Huard, Michaël Parmentier, Daisuke Hashizume, Ayako Nakamura, Yuki Kitamura, Shōko Suzuki and Olivier Leogane and has published in prestigious journals such as Journal of the American Chemical Society, Angewandte Chemie International Edition and Nature Communications.

In The Last Decade

Sylvain Lectard

11 papers receiving 940 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Sylvain Lectard Japan 10 884 281 236 120 29 11 948
En‐Ze Lin China 17 847 1.0× 435 1.5× 191 0.8× 62 0.5× 23 0.8× 23 917
Miaolin Ke China 16 759 0.9× 227 0.8× 177 0.8× 85 0.7× 44 1.5× 34 842
Haihui Peng China 12 860 1.0× 228 0.8× 157 0.7× 68 0.6× 38 1.3× 18 946
Thomas Scattolin Germany 18 847 1.0× 511 1.8× 300 1.3× 131 1.1× 57 2.0× 28 1.0k
Satoshi Okusu Japan 13 462 0.5× 369 1.3× 161 0.7× 82 0.7× 15 0.5× 14 564
Ryu Sakamoto Japan 21 893 1.0× 189 0.7× 212 0.9× 114 0.9× 17 0.6× 32 971
Wei‐Hao Rao China 17 1.6k 1.8× 143 0.5× 288 1.2× 83 0.7× 23 0.8× 32 1.6k
Zhenming Zhang China 20 821 0.9× 113 0.4× 176 0.7× 74 0.6× 22 0.8× 47 890
Devireddy Anand China 14 735 0.8× 289 1.0× 93 0.4× 89 0.7× 17 0.6× 15 797
Jian Wen China 14 816 0.9× 98 0.3× 165 0.7× 88 0.7× 24 0.8× 16 844

Countries citing papers authored by Sylvain Lectard

Since Specialization
Citations

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

Fields of papers citing papers by Sylvain Lectard

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sylvain Lectard

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

All Works

11 of 11 papers shown
1.
Sohtome, Yoshihiro, Shinsuke Komagawa, Ayako Nakamura, et al.. (2023). Experimental and Computational Investigation of Facial Selectivity Switching in Nickel–Diamine–Acetate-Catalyzed Michael Reactions. The Journal of Organic Chemistry. 88(12). 7764–7773. 1 indexed citations
2.
Sohtome, Yoshihiro, Atsuya Muranaka, Daisuke Hashizume, et al.. (2017). Naked d-orbital in a centrochiral Ni(II) complex as a catalyst for asymmetric [3+2] cycloaddition. Nature Communications. 8(1). 14875–14875. 36 indexed citations
3.
Suzuki, Shōko, Yuki Kitamura, Sylvain Lectard, Yoshitaka Hamashima, & Mikiko Sodeoka. (2012). Catalytic Asymmetric Mono‐Fluorination of α‐Keto Esters: Synthesis of Optically Active β‐Fluoro‐α‐Hydroxy and β‐Fluoro‐α‐Amino Acid Derivatives. Angewandte Chemie International Edition. 51(19). 4581–4585. 62 indexed citations
4.
Suzuki, Shōko, Yuki Kitamura, Sylvain Lectard, Yoshitaka Hamashima, & Mikiko Sodeoka. (2012). Catalytic Asymmetric Mono‐Fluorination of α‐Keto Esters: Synthesis of Optically Active β‐Fluoro‐α‐Hydroxy and β‐Fluoro‐α‐Amino Acid Derivatives. Angewandte Chemie. 124(19). 4659–4663. 18 indexed citations
5.
Nakamura, Ayako, Sylvain Lectard, Ryo Shimizu, Yoshitaka Hamashima, & Mikiko Sodeoka. (2010). Asymmetric conjugate addition of α-keto esters to nitroolefins catalyzed by chiral CuII hydroxo complexes. Tetrahedron Asymmetry. 21(13-14). 1682–1687. 18 indexed citations
6.
Lectard, Sylvain, Yoshitaka Hamashima, & Mikiko Sodeoka. (2010). Recent Advances in Catalytic Enantioselective Fluorination Reactions. Advanced Synthesis & Catalysis. 352(16). 2708–2732. 247 indexed citations
7.
Nakamura, Ayako, Sylvain Lectard, Daisuke Hashizume, Yoshitaka Hamashima, & Mikiko Sodeoka. (2010). Diastereo- and Enantioselective Conjugate Addition of α-Ketoesters to Nitroalkenes Catalyzed by a Chiral Ni(OAc)2 Complex under Mild Conditions. Journal of the American Chemical Society. 132(12). 4036–4037. 102 indexed citations
8.
Makino, Kazuishi, et al.. (2009). Enantioselective aziridination reaction of α,β-unsaturated aldehydes using an organocatalyst and tert-butyl N-arenesulfonyloxycarbamates. Tetrahedron Letters. 50(26). 3329–3332. 63 indexed citations
9.
Lebel, H., Sylvain Lectard, & Michaël Parmentier. (2007). Copper-Catalyzed Alkene Aziridination with N-Tosyloxycarbamates. Organic Letters. 9(23). 4797–4800. 85 indexed citations
10.
Lebel, H., Olivier Leogane, Kim Huard, & Sylvain Lectard. (2006). Catalytic activation of nitrogen derivatives with transition-metal complexes. Pure and Applied Chemistry. 78(2). 363–375. 55 indexed citations
11.
Lebel, H., Kim Huard, & Sylvain Lectard. (2005). N-Tosyloxycarbamates as a Source of Metal Nitrenes:  Rhodium-Catalyzed C−H Insertion and Aziridination Reactions. Journal of the American Chemical Society. 127(41). 14198–14199. 261 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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