David J. Slatkin

1.3k total citations
74 papers, 985 citations indexed

About

David J. Slatkin is a scholar working on Organic Chemistry, Plant Science and Molecular Biology. According to data from OpenAlex, David J. Slatkin has authored 74 papers receiving a total of 985 indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Organic Chemistry, 22 papers in Plant Science and 21 papers in Molecular Biology. Recurrent topics in David J. Slatkin's work include Traditional and Medicinal Uses of Annonaceae (21 papers), Chemical synthesis and alkaloids (18 papers) and Alkaloids: synthesis and pharmacology (15 papers). David J. Slatkin is often cited by papers focused on Traditional and Medicinal Uses of Annonaceae (21 papers), Chemical synthesis and alkaloids (18 papers) and Alkaloids: synthesis and pharmacology (15 papers). David J. Slatkin collaborates with scholars based in United States, Ghana and Egypt. David J. Slatkin's co-authors include Joseph E. Knapp, Paul L. Schiff, P.L. Schiff, D. Dwuma-Badu, Carlton E. Turner, Albert N. Tackie, A. B. Ray, Michael A. Zemaitis, Norman J. Doorenbos and Zhi-Jiang Zhang and has published in prestigious journals such as Cellular and Molecular Life Sciences, Tetrahedron and Life Sciences.

In The Last Decade

David J. Slatkin

72 papers receiving 899 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
David J. Slatkin United States 18 379 275 271 261 183 74 985
P.L. Schiff United States 16 281 0.7× 184 0.7× 208 0.8× 168 0.6× 160 0.9× 54 773
Sunil Kumar Talapatra India 18 488 1.3× 183 0.7× 267 1.0× 250 1.0× 168 0.9× 56 914
Satya P. Popli India 17 291 0.8× 135 0.5× 293 1.1× 210 0.8× 86 0.5× 49 703
A. B. Ray India 17 342 0.9× 152 0.6× 355 1.3× 169 0.6× 107 0.6× 56 1.1k
TOKUNOSUKE SAWADA Japan 18 419 1.1× 134 0.5× 269 1.0× 130 0.5× 79 0.4× 59 861
T. R. Seshadri India 18 518 1.4× 335 1.2× 342 1.3× 299 1.1× 60 0.3× 148 1.2k
Tokunaru Hòrie Japan 17 601 1.6× 279 1.0× 312 1.2× 337 1.3× 64 0.3× 91 1.2k
Otto Seligmann Germany 22 905 2.4× 161 0.6× 689 2.5× 185 0.7× 114 0.6× 76 1.4k
Mary Paı̈s France 19 572 1.5× 193 0.7× 263 1.0× 523 2.0× 170 0.9× 46 1.2k
Bani Talapatra India 17 395 1.0× 134 0.5× 198 0.7× 158 0.6× 103 0.6× 37 692

Countries citing papers authored by David J. Slatkin

Since Specialization
Citations

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

Fields of papers citing papers by David J. Slatkin

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by David J. Slatkin. 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 David J. Slatkin. The network helps show where David J. Slatkin may publish in the future.

Co-authorship network of co-authors of David J. Slatkin

This figure shows the co-authorship network connecting the top 25 collaborators of David J. Slatkin. A scholar is included among the top collaborators of David J. Slatkin 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 David J. Slatkin. David J. Slatkin 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.
Li, Youfu, et al.. (2004). The Effect of Temperature Variation In Vitro on Platelet-Leukocyte Interactions and Individual Prothrombotic Potential. Journal of Thrombosis and Thrombolysis. 18(1). 19–23. 4 indexed citations
2.
Lin, Fu‐Tyan, et al.. (1992). Alkaloids ofThalictrum glandulosissimum. Planta Medica. 58(1). 114–114. 11 indexed citations
3.
Omar, Abdallah A., et al.. (1987). Chemical Constituents ofCentaurea pallescens. Planta Medica. 53(5). 503–504. 11 indexed citations
4.
Fujii, Tozo, et al.. (1986). Racemic and Chiral Syntheses of the Alangium Alkaloid Alancine. Heterocycles. 24(2). 345–345.
5.
El‐Shanawany, Mohamed A., et al.. (1985). A NEW ALKALOID FROM OXANDRA XYLOPIOIDES DIELS. Bulletin of Pharmaceutical Sciences Assiut. 8(1). 127–143. 5 indexed citations
6.
Maurya, Rupesh, A. B. Ray, Shyamal Kumar Chattopadhyay, et al.. (1985). The Synthesis of Propterol, a Novel 1,3-Diarylpropan-2-ol from Pterocarpus marsupium. Journal of Natural Products. 48(2). 313–315. 4 indexed citations
7.
El-Fishawy, Ahlam M., David J. Slatkin, Joseph E. Knapp, & P.L. Schiff. (1984). Preparation of 7,8-Dimethoxy-3,4-dihydroisoquinoline, Facile Route to 7,8-Dioxygenated-3,4-dihydroisoquinolines. Journal of Pharmaceutical Sciences. 73(11). 1639–1640.
8.
Sahai, Mahendra, et al.. (1984). Physalolactone C, a New Withanolide from Physalis peruviana. Journal of Natural Products. 47(4). 648–651. 23 indexed citations
9.
Stiff, Dwight D., et al.. (1983). The lack of effectiveness of (−)-epicatechin against alloxan induced diabetes in Wistar rats. Life Sciences. 33(7). 593–597. 17 indexed citations
10.
11.
Svoboda, Gordon H., et al.. (1980). Chemical Constituents of Curatella Americana (Dilleniaceae). Journal of Pharmaceutical Sciences. 69(3). 360–361. 18 indexed citations
12.
Tackie, Albert N., et al.. (1980). Isolation of funiferine dimethiodide and oblongine from Tiliacora funifera. Phytochemistry. 19(8). 1882–1883. 9 indexed citations
13.
Svoboda, Gordon H., et al.. (1979). Chemical Constituents of Echites hirsuta (Apocynaceae). Journal of Pharmaceutical Sciences. 68(2). 247–249. 10 indexed citations
14.
Schiff, Paul L., et al.. (1978). Gilletine, a New Bisbenzylisoquinoline Alkaloid from Triclisia gilletii. Heterocycles. 9(8). 995–995. 1 indexed citations
15.
ElSohly, Mahmoud A., Carlton E. Turner, Charles H. Phoebe, et al.. (1978). Anhydrocannabisativine, a New Alkaloid from Cannabis sativa L.. Journal of Pharmaceutical Sciences. 67(1). 124–124. 33 indexed citations
16.
ElSohly, Mahmoud A., Joseph E. Knapp, Paul L. Schiff, & David J. Slatkin. (1976). Chemical constituents of fruit of Cocculus carolinus D. C. (menispermaceae). Journal of Pharmaceutical Sciences. 65(1). 132–133. 4 indexed citations
17.
Tackie, Albert N., D. Dwuma-Badu, Hala N. ElSohly, et al.. (1975). N-Isobutyloctadeca-trans-2-trans-4-dienamide: A new constituent of Piper guineense. Phytochemistry. 14(8). 1888–1889. 11 indexed citations
18.
ElSohly, Mahmoud A., Joseph E. Knapp, David J. Slatkin, et al.. (1974). Euparone, a New Benzofuran from Ruscus Aculeatus L.. Journal of Pharmaceutical Sciences. 63(10). 1623–1624. 20 indexed citations
19.
Tackie, Albert N., et al.. (1974). Tiliageine: A newbisbenzylisoquinoline biphenyl alkaloid fromTiliacora dinklagei. Cellular and Molecular Life Sciences. 30(8). 847–848. 12 indexed citations
20.
Weber, Nikolaus, Joseph E. Knapp, David J. Slatkin, et al.. (1974). Comparison of cocsuline with efirine, trigilletine and N-methyl-12′-O-desmethyltrilobin. Phytochemistry. 13(10). 2326–2326. 1 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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