Phyllis A. Leber

444 total citations
40 papers, 358 citations indexed

About

Phyllis A. Leber is a scholar working on Organic Chemistry, Atomic and Molecular Physics, and Optics and Physical and Theoretical Chemistry. According to data from OpenAlex, Phyllis A. Leber has authored 40 papers receiving a total of 358 indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Organic Chemistry, 11 papers in Atomic and Molecular Physics, and Optics and 10 papers in Physical and Theoretical Chemistry. Recurrent topics in Phyllis A. Leber's work include Asymmetric Synthesis and Catalysis (10 papers), Advanced Chemical Physics Studies (10 papers) and Catalysis and Oxidation Reactions (8 papers). Phyllis A. Leber is often cited by papers focused on Asymmetric Synthesis and Catalysis (10 papers), Advanced Chemical Physics Studies (10 papers) and Catalysis and Oxidation Reactions (8 papers). Phyllis A. Leber collaborates with scholars based in United States and Germany. Phyllis A. Leber's co-authors include John E. Baldwin, David C. Powers, Sarah S. Gallagher, Claude H. Yoder, Anuradha S. Raghavan, Randall S. Smith, Jared D. Bender, Kenneth R. Hess, Rajesh Shukla and Xavier Bogle and has published in prestigious journals such as Journal of the American Chemical Society, Accounts of Chemical Research and The Journal of Organic Chemistry.

In The Last Decade

Phyllis A. Leber

37 papers receiving 349 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Phyllis A. Leber United States 10 259 58 52 48 47 40 358
Marie‐Françoise Ruasse France 13 264 1.0× 44 0.8× 61 1.2× 59 1.2× 61 1.3× 23 351
Mark E. Jason United States 12 182 0.7× 42 0.7× 52 1.0× 45 0.9× 26 0.6× 21 269
Boriana Hadjieva Bulgaria 11 275 1.1× 93 1.6× 31 0.6× 93 1.9× 76 1.6× 25 391
G. LUTZ Germany 4 339 1.3× 34 0.6× 51 1.0× 26 0.5× 36 0.8× 5 398
Eduard Valentí Spain 11 561 2.2× 125 2.2× 55 1.1× 80 1.7× 41 0.9× 15 640
Mirko Sarzi-Amadè Italy 14 347 1.3× 73 1.3× 38 0.7× 31 0.6× 13 0.3× 21 430
Ana J. Royo Spain 11 260 1.0× 29 0.5× 103 2.0× 38 0.8× 57 1.2× 12 377
Giacomo Lo Moro Netherlands 11 198 0.8× 23 0.4× 72 1.4× 18 0.4× 46 1.0× 14 326
Marc A. van Bochove Netherlands 6 207 0.8× 94 1.6× 74 1.4× 41 0.9× 33 0.7× 8 341
Kevin A. Swiss United States 12 276 1.1× 48 0.8× 113 2.2× 32 0.7× 14 0.3× 19 353

Countries citing papers authored by Phyllis A. Leber

Since Specialization
Citations

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

Fields of papers citing papers by Phyllis A. Leber

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Phyllis A. Leber. 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 Phyllis A. Leber. The network helps show where Phyllis A. Leber may publish in the future.

Co-authorship network of co-authors of Phyllis A. Leber

This figure shows the co-authorship network connecting the top 25 collaborators of Phyllis A. Leber. A scholar is included among the top collaborators of Phyllis A. Leber 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 Phyllis A. Leber. Phyllis A. Leber 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.
Leber, Phyllis A., et al.. (2018). Stereoselectivity in a series of 7‐alkylbicyclo[3.2.0]hept‐2‐enes: Experimental and computational perspectives. Journal of Physical Organic Chemistry. 31(12). 5 indexed citations
2.
Leber, Phyllis A., et al.. (2013). A vinylcyclobutane substrate designed as a cyclopropylcarbinyl radical probe. Organic & Biomolecular Chemistry. 11(13). 2080–2080. 3 indexed citations
3.
Leber, Phyllis A., et al.. (2013). Experimental evidence of a cyclopropylcarbinyl conjugative electronic effect. Organic & Biomolecular Chemistry. 11(36). 5994–5994. 2 indexed citations
4.
Leber, Phyllis A., et al.. (2012). Thermal Isomerizations of cis,anti,cis-Tricyclo[7.4.0.02,8]tridec-10-ene. The Journal of Organic Chemistry. 77(7). 3468–3474. 3 indexed citations
5.
Yoder, Claude H., et al.. (2010). The Bridge to Organic Chemistry. 3 indexed citations
6.
Schilling, Amber, Phyllis A. Leber, & Claude H. Yoder. (2009). Exploration of SO2 Scrubbers: An Environmental Chemistry Project. Journal of Chemical Education. 86(2). 225–225. 2 indexed citations
7.
Leber, Phyllis A., Benjamin R. Williams, & Claude H. Yoder. (2009). The Change in Publication Rates at Undergraduate Institutions during the Last Three Decades. Journal of Chemical Education. 86(7). 876–876. 4 indexed citations
8.
Leber, Phyllis A., et al.. (2007). Effect of a Methoxy Substituent on the Vinylcyclobutane Carbon Migration. The Journal of Organic Chemistry. 72(3). 912–919. 10 indexed citations
9.
Baldwin, John E. & Phyllis A. Leber. (2007). Molecular rearrangements through thermal [1,3] carbon shifts. Organic & Biomolecular Chemistry. 6(1). 36–47. 53 indexed citations
10.
Bogle, Xavier, et al.. (2005). Thermal Reactions of 8-Methylbicyclo[4.2.0]oct-2-enes:  Competitive Diradical-Mediated [1,3] Sigmatropic, Stereomutation, and Fragmentation Processes. The Journal of Organic Chemistry. 70(22). 8913–8918. 15 indexed citations
11.
Baldwin, John E., Andrew R. Bogdan, Phyllis A. Leber, & David C. Powers. (2005). Thermal Isomerization of cis,anti,cis-Tricyclo[6.3.0.02,7]undec-3-ene to endo-Tricyclo[5.2.2.02,6]undec-8-ene. Organic Letters. 7(23). 5195–5197. 5 indexed citations
12.
Leber, Phyllis A., et al.. (2003). A Simple Method for Determination of Solubility in the First-Year Laboratory. Journal of Chemical Education. 80(5). 560–560. 7 indexed citations
13.
Baldwin, John E., et al.. (2001). Kinetics and Activation Parameters for the Thermal 1,5-Hydrogen Shifts Interconverting the Four Monodeuterio-cis,cis-1,3-cyclooctadienes. The Journal of Organic Chemistry. 66(15). 5269–5271. 8 indexed citations
14.
Baldwin, John E., et al.. (2001). Kinetic Derivations for Thermal Isomerizations of Monodeuterio Cyclic 1,3-Dienes through 1,5-Hydrogen Shifts. Journal of Chemical Education. 78(10). 1394–1394. 6 indexed citations
15.
Fluck, Richard A., et al.. (2000). Choline conjugates of auxins. I. Direct evidence for the hydrolysis of choline-auxin conjugates by pea cholinesterase. Plant Physiology and Biochemistry. 38(4). 301–308. 7 indexed citations
16.
Fluck, Richard A., et al.. (1995). A versatile and efficient methodology for the preparation of choline ester auxin conjugates. Phytochemistry. 40(4). 1027–1031. 2 indexed citations
17.
Glass, Timothy E., et al.. (1994). The thermal rearrangement of 7,7-dimethylbicyclo[3.2.0]hept-2-ene. Tetrahedron Letters. 35(17). 2675–2678. 2 indexed citations
18.
Leber, Phyllis A., et al.. (1986). The thermal rearrangement of endo-7-methyl-exo-7-vinylbicyclo[3.2.0]Hept-2-ene. Tetrahedron Letters. 27(35). 4107–4110. 5 indexed citations
19.
Leber, Phyllis A., et al.. (1982). Thermal rearrangements of encumbered methylenecyclobutanes. 1. 6-Methylenebicyclo[3.2.0]heptane. Journal of the American Chemical Society. 104(10). 2926–2927. 1 indexed citations
20.
Freudenthal, R. I., et al.. (1976). Characterization of the hepatic microsomal mixed-function oxidase enzyme system in miniature pigs.. Drug Metabolism and Disposition. 4(1). 25–27. 13 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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