Peter J. Crocker

431 total citations
21 papers, 352 citations indexed

About

Peter J. Crocker is a scholar working on Organic Chemistry, Pharmacology and Physical and Theoretical Chemistry. According to data from OpenAlex, Peter J. Crocker has authored 21 papers receiving a total of 352 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Organic Chemistry, 8 papers in Pharmacology and 6 papers in Physical and Theoretical Chemistry. Recurrent topics in Peter J. Crocker's work include Cannabis and Cannabinoid Research (7 papers), Chemical Reactions and Mechanisms (6 papers) and Synthesis and Catalytic Reactions (5 papers). Peter J. Crocker is often cited by papers focused on Cannabis and Cannabinoid Research (7 papers), Chemical Reactions and Mechanisms (6 papers) and Synthesis and Catalytic Reactions (5 papers). Peter J. Crocker collaborates with scholars based in United States, France and Germany. Peter J. Crocker's co-authors include David S. Watt, Raj K. Razdan, Billy R. Martin, Matthew S. Platz, Nobuyuki Imai, Stefan Kwiatkowski, Jenny L. Wiley, Anna D. Guđmundsdóttir, Anu Mahadevan and Thomas Vanaman and has published in prestigious journals such as Journal of Biological Chemistry, Journal of Medicinal Chemistry and Journal of Pharmacology and Experimental Therapeutics.

In The Last Decade

Peter J. Crocker

21 papers receiving 337 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Peter J. Crocker United States 11 157 127 121 82 64 21 352
Jesse A. May United States 14 329 2.1× 66 0.5× 340 2.8× 79 1.0× 49 0.8× 27 626
Hein K. A. C. Coolen Netherlands 12 379 2.4× 232 1.8× 202 1.7× 152 1.9× 15 0.2× 16 679
Willard M. Welch United States 14 460 2.9× 59 0.5× 270 2.2× 148 1.8× 32 0.5× 29 706
Mark A. Matulenko United States 13 242 1.5× 54 0.4× 332 2.7× 97 1.2× 25 0.4× 19 620
С. В. Курбатов Russia 13 462 2.9× 49 0.4× 125 1.0× 28 0.3× 108 1.7× 107 616
Miguel A. Toledo Spain 16 531 3.4× 51 0.4× 327 2.7× 173 2.1× 9 0.1× 30 864
Svend Treppendahl Denmark 11 225 1.4× 32 0.3× 219 1.8× 126 1.5× 42 0.7× 47 491
W. R. TULLY New Zealand 10 464 3.0× 44 0.3× 161 1.3× 72 0.9× 7 0.1× 18 622
C. Schall Germany 5 70 0.4× 141 1.1× 281 2.3× 36 0.4× 34 0.5× 5 446
Pier Luigi Ferrarini Italy 18 485 3.1× 214 1.7× 314 2.6× 145 1.8× 28 0.4× 35 793

Countries citing papers authored by Peter J. Crocker

Since Specialization
Citations

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

Fields of papers citing papers by Peter J. Crocker

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Peter J. Crocker

This figure shows the co-authorship network connecting the top 25 collaborators of Peter J. Crocker. A scholar is included among the top collaborators of Peter J. Crocker 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 Peter J. Crocker. Peter J. Crocker 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.
Beck, James P., Mark A. Wolf, Ning Xi, et al.. (2012). 4-Phenyl tetrahydroisoquinolines as dual norepinephrine and dopamine reuptake inhibitors. Bioorganic & Medicinal Chemistry Letters. 22(23). 7219–7222. 20 indexed citations
2.
Crocker, Peter J., Anu Mahadevan, Jenny L. Wiley, Billy R. Martin, & Raj K. Razdan. (2007). The role of fluorine substitution in the structure–activity relationships (SAR) of classical cannabinoids. Bioorganic & Medicinal Chemistry Letters. 17(6). 1504–1507. 6 indexed citations
3.
Wiley, Jenny L., et al.. (2002). Resorcinol Derivatives: A Novel Template for the Development of Cannabinoid CB1/CB2 and CB2-Selective Agonists. Journal of Pharmacology and Experimental Therapeutics. 301(2). 679–689. 48 indexed citations
4.
Martin, Billy R., Jenny L. Wiley, Brian F. Thomas, et al.. (2002). Assessment of structural commonality between tetrahydrocannabinol and anandamide. European Journal of Pharmacology. 435(1). 35–42. 8 indexed citations
5.
Bulychev, Alexey, E O’Brien, Peter J. Crocker, et al.. (2000). N-Sulfonyloxy-β-lactam Inhibitors for β-Lactamases. Tetrahedron. 56(31). 5719–5728. 16 indexed citations
6.
Griffin, Graeme, Peter J. Crocker, William J. Ryan, et al.. (1999). An investigation into the structural determinants of cannabinoid receptor ligand efficacy. British Journal of Pharmacology. 126(7). 1575–1584. 23 indexed citations
7.
Crocker, Peter J., Bijali Saha, William J. Ryan, et al.. (1999). Development of agonists, partial agonists and antagonists in the Δ8-Tetrahydrocannabinol series. Tetrahedron. 55(49). 13907–13926. 15 indexed citations
8.
Guđmundsdóttir, Anna D., et al.. (1998). A laser flash photolysis study of p-tolyl(trifluoromethyl)carbene. Journal of the Chemical Society Perkin Transactions 2. 1093–1100. 43 indexed citations
9.
Ryan, William J., et al.. (1997). Synthesis of (+)- and (−)-2-methylarachidonyl-2′-fluoroethylamide (O-689). Bioorganic & Medicinal Chemistry Letters. 7(20). 2669–2672. 1 indexed citations
10.
11.
12.
Crocker, Peter J. & Marvin J. Miller. (1995). Oxidative free-radical cyclization as a method for annulating .beta.-lactams: syntheses of functionalized carbacephams. The Journal of Organic Chemistry. 60(19). 6176–6179. 8 indexed citations
13.
14.
Drake, Richard R., James T. Slama, Katherine A. Wall, et al.. (1992). Application of an N-(4-azido-2,3,5,6-tetrafluorobenzoyl)tyrosine-substituted peptide as a heterobifunctional cross-linking agent in a study of protein O-glycosylation in yeast. Bioconjugate Chemistry. 3(1). 69–73. 17 indexed citations
15.
16.
Platz, Matthew S., et al.. (1991). Photolysis of 3-aryl-3-(trifluoromethyl)diazirines: a caveat regarding their use in photoaffinity probes. Bioconjugate Chemistry. 2(5). 337–341. 39 indexed citations
17.
Leyva, Elisa, et al.. (1991). THE PHOTOCHEMISTRY OF IODO, METHYL AND THIOMETHYL SUBSTITUTED ARYL AZIDES IN TOLUENE SOLUTION AND FROZEN POLYCRYSTALS. Photochemistry and Photobiology. 54(3). 329–333. 9 indexed citations
18.
Imai, Nobuyuki, Tadashi Kometani, Peter J. Crocker, et al.. (1990). Photoaffinity heterobifunctional crosslinking reagents based on N-(azidobenzoyl)tyrosines. Bioconjugate Chemistry. 1(2). 138–143. 7 indexed citations
19.
Crocker, Peter J., et al.. (1990). Heterobifunctional cross-linking agents incorporating perfluorinated aryl azides. Bioconjugate Chemistry. 1(6). 419–424. 28 indexed citations
20.
Kwiatkowski, Stefan, Peter J. Crocker, Ashok J. Chavan, et al.. (1990). Thiazolidine and thiazoline derivatives of 3-aryl-3-trifluoromethyldiazirines for the preparation of fluorescent or 35S-radiolabeled photoaffinity probes. Tetrahedron Letters. 31(15). 2093–2096. 18 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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