Johnnie L. Leazer

2.0k total citations · 1 hit paper
13 papers, 1.7k citations indexed

About

Johnnie L. Leazer is a scholar working on Organic Chemistry, Molecular Biology and Insect Science. According to data from OpenAlex, Johnnie L. Leazer has authored 13 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Organic Chemistry, 3 papers in Molecular Biology and 2 papers in Insect Science. Recurrent topics in Johnnie L. Leazer's work include Synthetic Organic Chemistry Methods (5 papers), Asymmetric Synthesis and Catalysis (4 papers) and Insect and Pesticide Research (2 papers). Johnnie L. Leazer is often cited by papers focused on Synthetic Organic Chemistry Methods (5 papers), Asymmetric Synthesis and Catalysis (4 papers) and Insect and Pesticide Research (2 papers). Johnnie L. Leazer collaborates with scholars based in United States and United Kingdom. Johnnie L. Leazer's co-authors include Russell J. Linderman, Kurt Lorenz, Julie B. Manley, Peter J. Dunn, Tony Y. Zhang, John Hayler, A. S. Zaks, Andrew S. Wells, Guy R. Humphrey and David J. C. Constable and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of the American Chemical Society and Environmental Science & Technology.

In The Last Decade

Johnnie L. Leazer

13 papers receiving 1.6k citations

Hit Papers

Key green chemistry research areas—a perspective from pha... 2007 2026 2013 2019 2007 400 800 1.2k

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Johnnie L. Leazer United States 12 1.2k 806 474 155 115 13 1.7k
Bruce A. Pearlman United States 10 1.2k 1.0× 767 1.0× 465 1.0× 167 1.1× 107 0.9× 15 1.6k
Tony Y. Zhang United States 21 1.9k 1.5× 880 1.1× 657 1.4× 199 1.3× 114 1.0× 34 2.4k
Joseph P. Adams United Kingdom 20 1.0k 0.8× 784 1.0× 278 0.6× 244 1.6× 89 0.8× 44 1.7k
Louis J. Diorazio United Kingdom 19 760 0.6× 353 0.4× 366 0.8× 129 0.8× 191 1.7× 51 1.2k
Jonathan D. Moseley United Kingdom 24 1.3k 1.1× 360 0.4× 228 0.5× 301 1.9× 50 0.4× 58 1.8k
Nicoletta Gaggero Italy 24 684 0.5× 811 1.0× 393 0.8× 150 1.0× 28 0.2× 56 1.6k
Fred J. Fleitz United States 13 954 0.8× 1.3k 1.6× 219 0.5× 305 2.0× 46 0.4× 19 2.0k
Thierry Le Gall France 24 2.0k 1.6× 606 0.8× 605 1.3× 69 0.4× 34 0.3× 81 2.7k
Ross M. Denton United Kingdom 26 1.6k 1.3× 602 0.7× 488 1.0× 96 0.6× 114 1.0× 49 2.1k
Hans Iding Switzerland 19 761 0.6× 1.4k 1.8× 298 0.6× 322 2.1× 37 0.3× 44 2.0k

Countries citing papers authored by Johnnie L. Leazer

Since Specialization
Citations

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

Fields of papers citing papers by Johnnie L. Leazer

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Johnnie L. Leazer

This figure shows the co-authorship network connecting the top 25 collaborators of Johnnie L. Leazer. A scholar is included among the top collaborators of Johnnie L. Leazer 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 Johnnie L. Leazer. Johnnie L. Leazer is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

13 of 13 papers shown
2.
Constable, David J. C., Peter J. Dunn, John Hayler, et al.. (2007). Key green chemistry research areas—a perspective from pharmaceutical manufacturers. Green Chemistry. 9(5). 411–420. 1306 indexed citations breakdown →
3.
Dormer, Peter G., Johnnie L. Leazer, Fengrui Lang, et al.. (2004). syn -2,3-Disubstituted-2,3-dihydro-1,4-benzoxathiin rings: preparation from quinone ketals and 2-mercaptoethanols. Tetrahedron Letters. 45(28). 5429–5432. 5 indexed citations
4.
Song, Zhiguo J., Anthony O. King, Fengrui Lang, et al.. (2004). An efficient asymmetric synthesis of an estrogen receptor modulator by sulfoxide-directed borane reduction. Proceedings of the National Academy of Sciences. 101(16). 5776–5781. 22 indexed citations
5.
Leazer, Johnnie L., et al.. (2003). An Improved Preparation of 3,5-Bis(trifluoromethyl)acetophenone and Safety Considerations in the Preparation of 3,5-Bis(trifluoromethyl)phenyl Grignard Reagent. The Journal of Organic Chemistry. 68(9). 3695–3698. 48 indexed citations
6.
Smith, Amos B., Stephen M. Condon, John A. McCauley, et al.. (1997). A Unified Total Synthesis of the Immunomodulators (−)-Rapamycin and (−)-27-Demethoxyrapamycin:  Assembly of the Common C(1−20) Perimeter and Final Elaboration. Journal of the American Chemical Society. 119(5). 962–973. 65 indexed citations
7.
Smith, Amos B., Stephen M. Condon, John A. McCauley, et al.. (1997). A Unified Total Synthesis of the Immunomodulators (−)-Rapamycin and (−)-27-Demethoxyrapamycin:  Construction of the C(21−42) Perimeters. Journal of the American Chemical Society. 119(5). 947–961. 59 indexed citations
8.
Smith, Amos B., Stephen M. Condon, John A. McCauley, et al.. (1995). Total Synthesis of Rapamycin and Demethoxyrapamycin. Journal of the American Chemical Society. 117(19). 5407–5408. 57 indexed citations
9.
Smith, Amos B., Robert E. Maleczka, Johnnie L. Leazer, et al.. (1994). Rapamycin synthetic studies. 2. Elaboration of the C(10)-C(26) perimeter. Tetrahedron Letters. 35(28). 4911–4914. 11 indexed citations
10.
Smith, Amos B., Stephen M. Condon, John A. McCauley, et al.. (1994). Rapamycin synthetic studies. 1. Construction of the C(27)-C(42) subunit. Tetrahedron Letters. 35(28). 4907–4910. 12 indexed citations
11.
Roe, R. Michael, et al.. (1990). Rational design and synthesis of polarized ketones as inhibitors of juvenile hormone esterase: importance of juvenile hormone mimicry. Journal of Agricultural and Food Chemistry. 38(5). 1274–1278. 18 indexed citations
12.
Linderman, Russell J., Johnnie L. Leazer, R. Michael Roe, et al.. (1988). 19F-NMR spectral evidence that 3-octylthio-1,1,1-trifluoropropan-2-one, a potent inhibitor of insect juvenile hormone esterase, functions as a transition state analog inhibitor of acetylcholinesterase. Pesticide Biochemistry and Physiology. 31(2). 187–194. 35 indexed citations
13.
Linderman, Russell J., Johnnie L. Leazer, Krishnappa Venkatesh, & R. Michael Roe. (1987). The inhibition of insect juvenile hormone esterase by trifluoromethylketones: Steric parameters at the active site. Pesticide Biochemistry and Physiology. 29(3). 266–277. 35 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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