Edward G. Corley

2.3k total citations
39 papers, 1.6k citations indexed

About

Edward G. Corley is a scholar working on Organic Chemistry, Molecular Biology and Spectroscopy. According to data from OpenAlex, Edward G. Corley has authored 39 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 32 papers in Organic Chemistry, 15 papers in Molecular Biology and 5 papers in Spectroscopy. Recurrent topics in Edward G. Corley's work include Asymmetric Synthesis and Catalysis (15 papers), Chemical Synthesis and Analysis (8 papers) and Synthesis and Catalytic Reactions (5 papers). Edward G. Corley is often cited by papers focused on Asymmetric Synthesis and Catalysis (15 papers), Chemical Synthesis and Analysis (8 papers) and Synthesis and Catalytic Reactions (5 papers). Edward G. Corley collaborates with scholars based in United States and Japan. Edward G. Corley's co-authors include Edward J. J. Grabowski, Robert D. Larsen, Paul J. Reider, Andrew S. Thompson, Martha Huntington, Thomas R. Verhoeven, James D. Carroll, Anthony O. King, Jerry A. Murry and David M. Tschaen and has published in prestigious journals such as Journal of the American Chemical Society, The Journal of Organic Chemistry and Tetrahedron.

In The Last Decade

Edward G. Corley

38 papers receiving 1.5k citations

Peers

Edward G. Corley
Edward G. Corley
Citations per year, relative to Edward G. Corley Edward G. Corley (= 1×) peers Gianni Palmieri

Countries citing papers authored by Edward G. Corley

Since Specialization
Citations

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

Fields of papers citing papers by Edward G. Corley

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Edward G. Corley. 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 Edward G. Corley. The network helps show where Edward G. Corley may publish in the future.

Co-authorship network of co-authors of Edward G. Corley

This figure shows the co-authorship network connecting the top 25 collaborators of Edward G. Corley. A scholar is included among the top collaborators of Edward G. Corley 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 Edward G. Corley. Edward G. Corley 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.
Xu, Feng, Edward G. Corley, Michael J. Zacuto, et al.. (2010). Asymmetric Synthesis of a Potent, Aminopiperidine-Fused Imidazopyridine Dipeptidyl Peptidase IV Inhibitor. The Journal of Organic Chemistry. 75(5). 1343–1353. 37 indexed citations
2.
Xu, Feng, Edward G. Corley, Jerry A. Murry, & David M. Tschaen. (2007). Highly Selective Cascade Couplings for the Syntheses of Functionalized Piperidinones and Bispidines.. ChemInform. 38(44). 1 indexed citations
3.
Brands, Karel M. J., Shane W. Krska, Thorsten Rosner, et al.. (2005). Understanding the Origin of Unusual Stepwise Hydrogenation Kinetics in the Synthesis of the 3-(4-Fluorophenyl)morpholine Moiety of NK1 Receptor Antagonist Aprepitant. Organic Process Research & Development. 10(1). 109–117. 13 indexed citations
4.
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
5.
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
6.
Davies, Ian W., Jean-François Marcoux, Edward G. Corley, et al.. (2000). A Practical Synthesis of a COX-2-Specific Inhibitor. The Journal of Organic Chemistry. 65(25). 8415–8420. 61 indexed citations
7.
Marcoux, Jean-François, Edward G. Corley, Kai Rossen, et al.. (2000). Annulation of Ketones with Vinamidinium Hexafluorophosphate Salts:  An Efficient Preparation of Trisubstituted Pyridines. Organic Letters. 2(15). 2339–2341. 39 indexed citations
8.
Thompson, Andrew S., Edward G. Corley, Martha Huntington, et al.. (1998). Lithium Ephedrate-Mediated Addition of a Lithium Acetylide to a Ketone:  Solution Structures and Relative Reactivities of Mixed Aggregates Underlying the High Enantioselectivities. Journal of the American Chemical Society. 120(9). 2028–2038. 136 indexed citations
9.
Larsen, Robert D., Edward G. Corley, Anthony O. King, et al.. (1996). Practical Route to a New Class of LTD4 Receptor Antagonists. The Journal of Organic Chemistry. 61(10). 3398–3405. 202 indexed citations
10.
Thompson, Andrew S., Edward G. Corley, Martha Huntington, & Edward J. J. Grabowski. (1995). Use of an ephedrine alkoxide to mediate enantioselective addition of an acetylide to a prochiral ketone: asymmetric synthesis of the reverse transcriptase inhibitor L-743,726. Tetrahedron Letters. 36(49). 8937–8940. 113 indexed citations
11.
Larsen, Robert D., Anthony O. King, Cheng‐Yu Chen, et al.. (1994). Efficient Synthesis of Losartan, A Nonpeptide Angiotensin II Receptor Antagonist. The Journal of Organic Chemistry. 59(21). 6391–6394. 137 indexed citations
12.
Senanayake, Chris H., Robert D. Larsen, Timothy J. Bill, et al.. (1994). Enantioselective Synthesis of 1,3-Dioxygen-substituted Chiral Building Blocks. Synlett. 1994(3). 199–200. 25 indexed citations
13.
King, Anthony O., Edward G. Corley, Robert D. Larsen, et al.. (1993). An efficient synthesis of LTD4 antagonist L-699,392. The Journal of Organic Chemistry. 58(14). 3731–3735. 79 indexed citations
14.
Mathre, David J., Andrew S. Thompson, Alan W. Douglas, et al.. (1993). A practical process for the preparation of tetrahydro-1-methyl-3,3-diphenyl-1H,3H-pyrrolo[1,2-c][1,3,2]oxazaborole-borane. A highly enantioselective stoichiometric and catalytic reducing agent. The Journal of Organic Chemistry. 58(10). 2880–2888. 166 indexed citations
15.
Larsen, Robert D., et al.. (1990). Synthesis of (5R,10S,11R)-(+)-10,11-dihydro-5-methyl-5H-dibenzo[a,d]cyclohepten-5,10-imin-11-ol: a hydroxylated metabolite of MK-0801. The Journal of Organic Chemistry. 55(1). 299–304. 9 indexed citations
16.
Karady, Sandor, et al.. (1989). Cyclization of electrochemically generated nitrogen radicals. A novel synthesis of 11-substituted dibenzo[a,d]cycloheptenimines. Tetrahedron Letters. 30(17). 2191–2194. 17 indexed citations
17.
Corley, Edward G., et al.. (1988). Anodic N-dearylation of 2-azetidinones. Tetrahedron Letters. 29(13). 1497–1500. 18 indexed citations
18.
Sletzinger, M., et al.. (1985). A diastereospecific, non-racemic synthesis of a novel β-hydroxy-δ-lactone HMG-CoA reductase inhibitor. Tetrahedron Letters. 26(25). 2951–2954. 47 indexed citations
19.
Heindel, Ned D., et al.. (1982). A new radioiodination procedure for pharmaceuticals: Triazene decomposition. International Journal of Nuclear Medicine and Biology. 9(3). 222–222. 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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