Soth Samreth

509 total citations
24 papers, 370 citations indexed

About

Soth Samreth is a scholar working on Organic Chemistry, Molecular Biology and Pharmacology. According to data from OpenAlex, Soth Samreth has authored 24 papers receiving a total of 370 indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Organic Chemistry, 12 papers in Molecular Biology and 4 papers in Pharmacology. Recurrent topics in Soth Samreth's work include Carbohydrate Chemistry and Synthesis (12 papers), Glycosylation and Glycoproteins Research (5 papers) and Chemical Synthesis and Analysis (5 papers). Soth Samreth is often cited by papers focused on Carbohydrate Chemistry and Synthesis (12 papers), Glycosylation and Glycoproteins Research (5 papers) and Chemical Synthesis and Analysis (5 papers). Soth Samreth collaborates with scholars based in France, United States and Canada. Soth Samreth's co-authors include Michel Farnier, François Bellamy, J. Millet, Derek Horton, Claude Paulmier, Laurence Hecquet, Patrice Renaut, Franck Charmantray, Francis Schuber and F. BELLAMY and has published in prestigious journals such as Journal of Medicinal Chemistry, Electrochimica Acta and Inorganic Chemistry.

In The Last Decade

Soth Samreth

24 papers receiving 343 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Soth Samreth France 11 280 158 46 45 38 24 370
Carina Storm Poulsen Denmark 5 293 1.0× 153 1.0× 38 0.8× 30 0.7× 19 0.5× 6 403
Stephen W. Horgan United States 10 324 1.2× 108 0.7× 52 1.1× 28 0.6× 19 0.5× 16 470
Edward D. Robinson United States 10 362 1.3× 130 0.8× 28 0.6× 22 0.5× 19 0.5× 19 504
Johannes Häusler Austria 13 244 0.9× 202 1.3× 65 1.4× 26 0.6× 22 0.6× 32 399
Louis Hamon France 14 454 1.6× 144 0.9× 43 0.9× 26 0.6× 20 0.5× 36 522
Pierre Demerseman France 14 391 1.4× 149 0.9× 43 0.9× 49 1.1× 32 0.8× 62 520
N. Knouzi France 7 334 1.2× 145 0.9× 41 0.9× 35 0.8× 25 0.7× 21 435
David M. Hollinshead United Kingdom 13 320 1.1× 119 0.8× 26 0.6× 42 0.9× 26 0.7× 17 450
Yoshihiro Yoshida Japan 10 411 1.5× 155 1.0× 24 0.5× 29 0.6× 10 0.3× 18 478
Yolanda Pérez-Fuertes United Kingdom 11 315 1.1× 213 1.3× 85 1.8× 13 0.3× 25 0.7× 12 557

Countries citing papers authored by Soth Samreth

Since Specialization
Citations

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

Fields of papers citing papers by Soth Samreth

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Soth Samreth

This figure shows the co-authorship network connecting the top 25 collaborators of Soth Samreth. A scholar is included among the top collaborators of Soth Samreth 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 Soth Samreth. Soth Samreth 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.
Charmantray, Franck, Philippe Dellis, Virgil Hélaine, Soth Samreth, & Laurence Hecquet. (2006). Chemoenzymatic Synthesis of 5‐Thio‐D‐xylopyranose. European Journal of Organic Chemistry. 2006(24). 5526–5532. 17 indexed citations
2.
Charmantray, Franck, et al.. (2006). An efficient chemoenzymatic route to dihydroxyacetone phosphate from glycidol for the in situ aldolase-mediated synthesis of monosaccharides. Tetrahedron Letters. 47(19). 3261–3263. 22 indexed citations
3.
Brevet, David, Yves Mugnier, & Soth Samreth. (2003). Réactivité du bromure de 5-thioxylopyranosyle et du 1,5-dithioxylopyranoside vis-à-vis d’anions thiolate. Comptes Rendus Chimie. 6(4). 485–491. 1 indexed citations
4.
Brevet, David, Yves Mugnier, Soth Samreth, & Philippe Dellis. (2003). New efficient electrochemical synthesis of 1,5-dithioxylopyranosides in the presence of a sacrificial anode. Carbohydrate Research. 338(15). 1543–1552. 2 indexed citations
5.
Brevet, David, Yves Mugnier, Frédéric Lemaître, et al.. (2003). Stoichiometric and Catalytic Activation of the α- and β-2,3,4-Tri-O-Acetyl-5-Thioxylopyranosyl Bromide Inside the Cavity of the Pd3(dppm)3(CO)2+ Cluster. Inorganic Chemistry. 42(16). 4909–4917. 10 indexed citations
6.
Brevet, David, Yves Mugnier, & Soth Samreth. (2003). Efficient electrochemical synthesis of thioxylal. Electrochimica Acta. 48(23). 3419–3422. 2 indexed citations
7.
Li, Yun, et al.. (1999). Synthesis of the 3-methyl ether and 4-deoxy derivatives of 4-cyanophenyl 1,5-dithio-β-d-xylopyranoside (Beciparcil). Carbohydrate Research. 316(1-4). 104–111. 4 indexed citations
8.
Li, Yun, et al.. (1998). Chemical interconversions of 4-cyanophenyl 1,5-dithio-β-d-xylopyranoside (Beciparcil®): structural modification at the C-4 position. Carbohydrate Research. 314(3-4). 161–167. 3 indexed citations
9.
Baudry, Michel, et al.. (1998). Synthetic studies in the 5-thio-d-xylopyranose seriespart 3: Preparations ofO-phenyl andC-(4-hydroxyphenyl) 5-thio-d-xylopyranosides. Tetrahedron. 54(45). 13783–13792. 8 indexed citations
10.
Samreth, Soth, et al.. (1996). Structural and Stereoelectronic Requirements for the Inhibition of Mammalian 2,3-Oxidosqualene Cyclase by Substituted Isoquinoline Derivatives. Journal of Medicinal Chemistry. 39(12). 2302–2312. 22 indexed citations
11.
Bellamy, François, Niall M.B. Martin, Philippe Masson, et al.. (1995). THIOXYLOSIDE DERIVATIVES AS ORALLY ACTIVE VENOUS ANTITHROMBOTICS. European Journal of Medicinal Chemistry. 30. 101s–115s. 46 indexed citations
12.
Samreth, Soth, F. BELLAMY, Derek Horton, et al.. (1994). ChemInform Abstract: Thioxyloside Derivatives, a Novel Oral Venous Antithrombotic. ChemInform. 25(44). 1 indexed citations
13.
Bellamy, François, et al.. (1993). Glycosylated derivatives of benzophenone, benzhydrol and benzhydril as potential venous antithrombotic agents. Journal of Medicinal Chemistry. 36(7). 898–903. 47 indexed citations
14.
BELLAMY, F., et al.. (1990). Towards a new type-of HMG-COA reductase inhibitor. Tetrahedron. 46(19). 6731–6740. 17 indexed citations
15.
16.
Guilard, Roger, et al.. (1981). Synthèse de dérivés indoliques substitués in 7. Journal of Heterocyclic Chemistry. 18(7). 1373–1377. 7 indexed citations
17.
Samreth, Soth, et al.. (1978). Recherches en série hétérocyclique. XXIX. Sur des voies d'accès à des thiéno, sélénolo, furo et pyrrolopyrroles. Canadian Journal of Chemistry. 56(10). 1429–1434. 28 indexed citations
18.
Farnier, Michel, et al.. (1976). Recherches en série hétérocyclique. XXVIII. Synthèse de bipyrroles. Canadian Journal of Chemistry. 54(7). 1083–1086. 22 indexed citations
19.
20.
Farnier, Michel, et al.. (1976). Recherches en série hétérocyclique. XXVII. Etude de la condensation de l'azidoacétate d'éthyle sur les thiophènedicarbaldéhydes-2,5, -2,4 et -3,4. Canadian Journal of Chemistry. 54(7). 1074–1082. 20 indexed citations

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