Philip L. Stotter

507 total citations
24 papers, 365 citations indexed

About

Philip L. Stotter is a scholar working on Organic Chemistry, Molecular Biology and Pharmaceutical Science. According to data from OpenAlex, Philip L. Stotter has authored 24 papers receiving a total of 365 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Organic Chemistry, 9 papers in Molecular Biology and 4 papers in Pharmaceutical Science. Recurrent topics in Philip L. Stotter's work include Chemical Synthesis and Analysis (4 papers), Asymmetric Synthesis and Catalysis (3 papers) and Estrogen and related hormone effects (3 papers). Philip L. Stotter is often cited by papers focused on Chemical Synthesis and Analysis (4 papers), Asymmetric Synthesis and Catalysis (3 papers) and Estrogen and related hormone effects (3 papers). Philip L. Stotter collaborates with scholars based in United States. Philip L. Stotter's co-authors include Rex E. Hornish, David E. Minter, Mohammad Salman, Gary C. Chamness, Thomas H. Porter, Karl Folkers, B. Rami Reddy, S. J. Friedberg, G. Zając and James M. Gallas and has published in prestigious journals such as Journal of the American Chemical Society, Journal of Biological Chemistry and Journal of Medicinal Chemistry.

In The Last Decade

Philip L. Stotter

24 papers receiving 336 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Philip L. Stotter United States 13 213 127 49 31 31 24 365
Erwin F. Schoenewaldt United States 12 257 1.2× 253 2.0× 19 0.4× 44 1.4× 55 1.8× 16 464
Josef E. Herz Mexico 12 146 0.7× 209 1.6× 60 1.2× 25 0.8× 12 0.4× 46 422
A. R. Daniewski Poland 14 324 1.5× 153 1.2× 24 0.5× 39 1.3× 26 0.8× 36 431
Ivo Jirkovsky United States 13 326 1.5× 130 1.0× 35 0.7× 56 1.8× 23 0.7× 34 460
Isidoros Vlattas United States 13 417 2.0× 284 2.2× 30 0.6× 126 4.1× 53 1.7× 32 700
W. M. McLamore United States 11 426 2.0× 255 2.0× 25 0.5× 77 2.5× 31 1.0× 18 635
Paul Buchschacher Switzerland 10 298 1.4× 261 2.1× 57 1.2× 33 1.1× 56 1.8× 15 582
A. J. Manson United Kingdom 9 230 1.1× 179 1.4× 100 2.0× 32 1.0× 14 0.5× 14 412
Nobuaki Waizumi Japan 8 253 1.2× 108 0.9× 27 0.6× 54 1.7× 18 0.6× 8 368
F. W. Stonner United States 7 225 1.1× 168 1.3× 99 2.0× 28 0.9× 15 0.5× 9 400

Countries citing papers authored by Philip L. Stotter

Since Specialization
Citations

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

Fields of papers citing papers by Philip L. Stotter

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Philip L. Stotter. 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 Philip L. Stotter. The network helps show where Philip L. Stotter may publish in the future.

Co-authorship network of co-authors of Philip L. Stotter

This figure shows the co-authorship network connecting the top 25 collaborators of Philip L. Stotter. A scholar is included among the top collaborators of Philip L. Stotter 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 Philip L. Stotter. Philip L. Stotter 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.
Martinez, Rodolfo A., et al.. (2002). Large-Scale Preparation of [13C]Methyl Phenyl Sulfide from [13C]Methanol by a One-Step Process. Organic Process Research & Development. 6(6). 851–854. 5 indexed citations
2.
Gallas, James M., G. Zając, Tadeusz Sarna, & Philip L. Stotter. (2000). Structural Differences in Unbleached and Mildly‐Bleached Synthetic Tyrosine‐Derived Melanins Identified by Scanning Probe Microscopies. Pigment Cell Research. 13(2). 99–108. 29 indexed citations
3.
Salman, Mohammad, et al.. (1991). 17α -Substituted analogs of estradiol for the development of fluorescent estrogen receptor ligands. Steroids. 56(7). 375–387. 27 indexed citations
4.
Salman, Mohammad, Philip L. Stotter, & Gary C. Chamness. (1989). 125I-ligand for progesterone receptor: 17α-(6'-iodohex-1'-ynyl)-19-nortestosterone. Journal of Steroid Biochemistry. 33(1). 25–31. 10 indexed citations
5.
Martinez, Rodolfo A., et al.. (1988). Synthesis of regiospecifically labeled [18O]glycolic acid and [18O]acyldihydroxyacetone phosphate.. Journal of Lipid Research. 29(1). 94–101. 2 indexed citations
6.
Stotter, Philip L., et al.. (1987). Quinuclidine∑boranes as Intermediates in Formation and Isolation of Functionalized Quinuclidine Systems. Heterocycles. 25(1). 251–251. 17 indexed citations
7.
Stotter, Philip L., et al.. (1987). Facile Preparation of Two 5-(a-Acetoxyethyl)-3-quinuclidinones via Intramolecular Functionalization. Heterocycles. 25(1). 259–259. 4 indexed citations
8.
Salman, Mohammad, B. Rami Reddy, Suprabhat Ray, Philip L. Stotter, & Gary C. Chamness. (1986). 17α-Allyl estradiol analogues as candidates for development of high-affinity fluorescein-estradiol conjugates. Journal of Steroid Biochemistry. 24(2). 539–548. 20 indexed citations
9.
Stotter, Philip L., et al.. (1985). Model studies of a conceptually new approach to the total synthesis of quinine. The Journal of Organic Chemistry. 50(1). 29–31. 14 indexed citations
10.
Minter, David E. & Philip L. Stotter. (1982). ChemInform Abstract: EFFICIENT CONVERSIONS OF QUINOLINES TO N‐(CARBOALKOXY)‐1,2‐DIHYDROQUINOLINES. Chemischer Informationsdienst. 13(8). 1 indexed citations
11.
Minter, David E. & Philip L. Stotter. (1981). Efficient conversions of quinolines to N-(carboalkoxy)-1,2-dihydroquinolines. The Journal of Organic Chemistry. 46(20). 3965–3970. 16 indexed citations
12.
Friedberg, S. J., et al.. (1980). The mechanism of ether bond formation in O-alkyl lipid synthesis.. Journal of Biological Chemistry. 255(3). 1074–1079. 22 indexed citations
13.
Stotter, Philip L., et al.. (1975). γ-halotiglates, II. A high yield, stereoselective preparation and the conversion to useful trisubstituted olefin synthons. Tetrahedron Letters. 16(21). 1679–1682. 12 indexed citations
14.
Stotter, Philip L., et al.. (1974). .gamma.-Halotiglates. I. Simple, efficient position-specific annelation of unsymmetrically substituted cyclohexanones. Journal of the American Chemical Society. 96(20). 6524–6526. 12 indexed citations
15.
Stotter, Philip L. & Rex E. Hornish. (1973). New thiane chemistry. Conceptually simple and technically practical total synthesis of Cecropia juvenile hormones. Journal of the American Chemical Society. 95(13). 4444–4446. 38 indexed citations
16.
Stotter, Philip L., et al.. (1973). Selective ozonolysis of 2,4-dienoate esters: A convenient stereoselective preparation of 4-oxo and 4-hydroxy -2-alkenoates. Tetrahedron Letters. 14(26). 2417–2420. 28 indexed citations
17.
Stotter, Philip L., et al.. (1973). The Use of Modular Computer-Based Lessons in a Modification of the Classical Introductory Course in Organic Chemistry.. 1 indexed citations
18.
Stotter, Philip L., et al.. (1972). α-Halocarbonyl compounds, I. An efficient preparation of α-bromoesters and α-bromoacids. Tetrahedron Letters. 13(40). 4067–4070. 30 indexed citations
19.
Stotter, Philip L., et al.. (1972). Allylic functionalization of α-methylmuconates: A new synthesis of 2,5-dihydro-2,4-disubstituted thiophenes, furans, and pyrroles. Tetrahedron Letters. 13(40). 4071–4074. 6 indexed citations
20.
Stork, Gilbert & Philip L. Stotter. (1969). A New Approach to the Stereospecific Synthesis of Angularly Substituted Polycyclic Systems. Journal of the American Chemical Society. 91(27). 7780–7781. 7 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Erwin F. Schoenewaldt Breakdown of academic impact, for papers by Josef E. Herz Breakdown of academic impact, for papers by A. R. Daniewski Breakdown of academic impact, for papers by Ivo Jirkovsky Breakdown of academic impact, for papers by Isidoros Vlattas Breakdown of academic impact, for papers by W. M. McLamore Breakdown of academic impact, for papers by Paul Buchschacher Breakdown of academic impact, for papers by A. J. Manson Breakdown of academic impact, for papers by Nobuaki Waizumi Breakdown of academic impact, for papers by F. W. Stonner
Rankless by CCL
2026