Cécile Savarin

1.3k total citations
17 papers, 1.0k citations indexed

About

Cécile Savarin is a scholar working on Organic Chemistry, Inorganic Chemistry and Molecular Biology. According to data from OpenAlex, Cécile Savarin has authored 17 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Organic Chemistry, 5 papers in Inorganic Chemistry and 3 papers in Molecular Biology. Recurrent topics in Cécile Savarin's work include Sulfur-Based Synthesis Techniques (7 papers), Asymmetric Hydrogenation and Catalysis (5 papers) and Synthesis and Catalytic Reactions (5 papers). Cécile Savarin is often cited by papers focused on Sulfur-Based Synthesis Techniques (7 papers), Asymmetric Hydrogenation and Catalysis (5 papers) and Synthesis and Catalytic Reactions (5 papers). Cécile Savarin collaborates with scholars based in United States and Spain. Cécile Savarin's co-authors include Lanny S. Liebeskind, Jiří Šrogl, Matthew T. Tudge, Guy R. Humphrey, Minoru Tamiya, Jerry A. Murry, Peter G. Dormer, Edward G. Corley, Karen M. Conrad and Alan M. Allgeier and has published in prestigious journals such as Chemical Communications, The Journal of Organic Chemistry and Tetrahedron.

In The Last Decade

Cécile Savarin

17 papers receiving 1.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Cécile Savarin United States 14 929 133 106 95 76 17 1.0k
Bingxin Liu China 20 894 1.0× 93 0.7× 119 1.1× 100 1.1× 22 0.3× 31 958
Tiezheng Jia United States 25 1.6k 1.7× 88 0.7× 80 0.8× 153 1.6× 18 0.2× 45 1.7k
Sajal Das India 20 936 1.0× 135 1.0× 62 0.6× 107 1.1× 17 0.2× 57 1.0k
Yoshiaki Sugihara Japan 18 962 1.0× 78 0.6× 167 1.6× 81 0.9× 36 0.5× 96 1.1k
О. А. Тарасова Russia 17 909 1.0× 90 0.7× 173 1.6× 83 0.9× 71 0.9× 156 1.0k
Gary N. Hermann Germany 11 687 0.7× 126 0.9× 53 0.5× 139 1.5× 109 1.4× 12 792
Stéphane Perrio France 19 864 0.9× 88 0.7× 71 0.7× 107 1.1× 7 0.1× 44 936
Takane Uchida Japan 14 717 0.8× 102 0.8× 60 0.6× 54 0.6× 43 0.6× 84 797
Nataliya A. Belogorlova Russia 15 586 0.6× 54 0.4× 150 1.4× 240 2.5× 24 0.3× 101 773
Б. И. Бузыкин Russia 13 467 0.5× 106 0.8× 127 1.2× 73 0.8× 55 0.7× 81 587

Countries citing papers authored by Cécile Savarin

Since Specialization
Citations

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

Fields of papers citing papers by Cécile Savarin

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Cécile Savarin

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

All Works

17 of 17 papers shown
1.
Savarin, Cécile, et al.. (2011). Selective Catalytic Hydrogenation of Nitro Groups in the Presence of Activated Heteroaryl Halides. The Journal of Organic Chemistry. 76(23). 9841–9844. 29 indexed citations
2.
Tudge, Matthew T., Cécile Savarin, Peter E. Maligres, et al.. (2010). Development of a Kilogram-Scale Asymmetric Synthesis of a Potent DP Receptor Antagonist. Organic Process Research & Development. 14(4). 787–798. 13 indexed citations
3.
Thiel, Oliver R., Michał Achmatowicz, Charles Bernard, et al.. (2009). Development of a Practical Synthesis of a p38 MAP Kinase Inhibitor. Organic Process Research & Development. 13(2). 230–241. 16 indexed citations
4.
Tudge, Matthew T., et al.. (2007). Facile reduction of malonate derivatives using NaBH4/Br2: an efficient route to 1,3-diols. Tetrahedron Letters. 49(6). 1041–1044. 13 indexed citations
5.
Savarin, Cécile, et al.. (2007). Novel Intramolecular Reactivity of Oximes:  Synthesis of Cyclic and Spiro-Fused Imines. Organic Letters. 9(6). 981–983. 27 indexed citations
6.
Peresypkin, Andrey, Robert M. Wenslow, Narayan Variankaval, et al.. (2006). Development of a pharmaceutical cocrystal of a monophosphate salt with phosphoric acid. Chemical Communications. 419–421. 80 indexed citations
7.
Tudge, Matthew T., Minoru Tamiya, Cécile Savarin, & Guy R. Humphrey. (2006). Development of a Novel, Highly Efficient Halide-Catalyzed Sulfenylation of Indoles. Organic Letters. 8(4). 565–568. 180 indexed citations
8.
Tudge, Matthew T., Minoru Tamiya, Cécile Savarin, & Guy R. Humphrey. (2006). Development of a Novel, Highly Efficient Halide‐Catalyzed Sulfenylation of Indoles.. ChemInform. 37(26). 1 indexed citations
9.
Savarin, Cécile, et al.. (2006). Direct N-Acetyl Enamine Formation:  Lithium Bromide Mediated Addition of Methyllithium to Nitriles. Organic Letters. 8(18). 3903–3906. 28 indexed citations
10.
Corley, Edward G., et al.. (2004). Direct Synthesis of 4-Arylpiperidines via Palladium/Copper(I)-Cocatalyzed Negishi Coupling of a 4-Piperidylzinc Iodide with Aromatic Halides and Triflates. The Journal of Organic Chemistry. 69(15). 5120–5123. 45 indexed citations
11.
Savarin, Cécile, Jerry A. Murry, Karen M. Conrad, et al.. (2004). An efficient synthesis of a highly functionalized 4-arylpiperidine. Tetrahedron. 60(50). 11367–11374. 12 indexed citations
12.
Liebeskind, Lanny S., Jiří Šrogl, Cécile Savarin, & Concepción Polanco. (2002). Bioinspired organometallic chemistry. Pure and Applied Chemistry. 74(1). 115–122. 29 indexed citations
13.
Savarin, Cécile, Jiří Šrogl, & Lanny S. Liebeskind. (2002). A Mild, Nonbasic Synthesis of Thioethers. The Copper-Catalyzed Coupling of Boronic Acids with N-Thio(alkyl, aryl, heteroaryl)imides. Organic Letters. 4(24). 4309–4312. 240 indexed citations
14.
Savarin, Cécile, Jerry A. Murry, & Peter G. Dormer. (2002). An Expedient Synthesis of Highly Functionalized Naphthyridones and Quinolines from a Common N-Aryl Pyridinone Template. Organic Letters. 4(12). 2071–2074. 39 indexed citations
15.
Savarin, Cécile & Lanny S. Liebeskind. (2001). Nonbasic, Room Temperature, Palladium-Catalyzed Coupling of Aryl and Alkenyl Iodides with Boronic Acids Mediated by Copper(I) Thiophene-2-carboxylate (CuTC). Organic Letters. 3(14). 2149–2152. 78 indexed citations
16.
Savarin, Cécile, Jiří Šrogl, & Lanny S. Liebeskind. (2000). Thiol Ester−Boronic Acid Cross-Coupling. Catalysis Using Alkylative Activation of the Palladium Thiolate Intermediate. Organic Letters. 2(20). 3229–3231. 84 indexed citations
17.
Savarin, Cécile, Jiří Šrogl, & Lanny S. Liebeskind. (2000). Substituted Alkyne Synthesis under Nonbasic Conditions:  Copper Carboxylate-Mediated, Palladium-Catalyzed Thioalkyne−Boronic Acid Cross-Coupling. Organic Letters. 3(1). 91–93. 133 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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