Leo S. Geraci

1.1k total citations · 1 hit paper
9 papers, 938 citations indexed

About

Leo S. Geraci is a scholar working on Organic Chemistry, Pharmacology and Pharmacology. According to data from OpenAlex, Leo S. Geraci has authored 9 papers receiving a total of 938 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Organic Chemistry, 2 papers in Pharmacology and 2 papers in Pharmacology. Recurrent topics in Leo S. Geraci's work include Asymmetric Synthesis and Catalysis (4 papers), Synthetic Organic Chemistry Methods (4 papers) and Carbohydrate Chemistry and Synthesis (3 papers). Leo S. Geraci is often cited by papers focused on Asymmetric Synthesis and Catalysis (4 papers), Synthetic Organic Chemistry Methods (4 papers) and Carbohydrate Chemistry and Synthesis (3 papers). Leo S. Geraci collaborates with scholars based in United States and France. Leo S. Geraci's co-authors include Gary E. Keck, Stephen F. Martin, J. Howard Jones, Michael L. Jones, A. Thomas DiCioccio, Janet Sredy, J. L. Jacot, A. Podjarny, Diane R. Sawicki and David Gunn and has published in prestigious journals such as Journal of the American Chemical Society, Journal of Medicinal Chemistry and Tetrahedron.

In The Last Decade

Leo S. Geraci

9 papers receiving 896 citations

Hit Papers

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What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Catalytic asymmetric allylation of aldehydes

1993 425 citations Gary E. Keck, Leo S. Geraci et al. Journal of the American Chemical Society profile →

Peers

Countries citing papers authored by Leo S. Geraci

Since Specialization

Citations

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

Fields of papers citing papers by Leo S. Geraci

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Leo S. Geraci. 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 Leo S. Geraci. The network helps show where Leo S. Geraci may publish in the future.

Co-authorship network of co-authors of Leo S. Geraci

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

All Works

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9 of 9 papers shown

#	Work	Indexed citations
1	Discovery of 3-[(4,5,7-Trifluorobenzothiazol-2-yl)methyl]indole-N-acetic Acid (Lidorestat) and Congeners as Highly Potent and Selective Inhibitors of Aldose Reductase for Treatment of Chronic Diabetic Complications 2005 ·Journal of Medicinal Chemistry ·M.C. Van Zandt, Michael L. Jones, David Gunn, Leo S. Geraci, J. Howard Jones, Diane R. Sawicki, Janet Sredy, J. L. Jacot, A. Thomas DiCioccio, T. Petrova, A. Mitschler, A. Podjarny	205
2	Total Synthesis of (+)‐Ambruticin S. 2003 ·ChemInform ·(unknown), Robert J. Cherney, John Colucci, Christine Courillon, Leo S. Geraci, Thomas A. Kirkland, Matthew A. Marx, Matthias Schneider, Stephen F. Martin	1
3	Total synthesis of (+)-ambruticin S 2003 ·Tetrahedron ·(unknown), Robert J. Cherney, John Colucci, Christine Courillon, Leo S. Geraci, Thomas A. Kirkland, Matthew A. Marx, Matthias Schneider, Stephen F. Martin	44
4	Total Synthesis of (+)-Ambruticin S 2001 ·Journal of the American Chemical Society ·Thomas A. Kirkland, John Colucci, Leo S. Geraci, Matthew A. Marx, Matthias Schneider, David E. Kaelin, Stephen F. Martin	58
5	Catalytic asymmetric allylation (CAA) reactions. II. A new enantioselective allylation procedure 1993 ·Tetrahedron Letters ·Gary E. Keck, Leo S. Geraci	109
6	Catalytic asymmetric allylation of aldehydes breakdown → 1993 ·Journal of the American Chemical Society ·Gary E. Keck, (unknown), Leo S. Geraci	425
7	Unified strategy for synthesis of indole and 2-oxindole alkaloids 1991 ·Journal of the American Chemical Society ·Stephen F. Martin, J. E. Hunter, (unknown), Leo S. Geraci, Michael Mortimore	69
8	Radical-cation-initiated Diels-Alder di- and trimerization of 3,4-dimethoxypropenylbenzene: stereochemical correlation with the lignans galbulin and isogalbulin 1989 ·Journal of the American Chemical Society ·R. Marshall Wilson, (unknown), Timothy A. Shepherd, Douglas M. Ho, Karlyn A. Schnapp, R. C. Elder, J.W. Watkins, Leo S. Geraci, Charles F. Campana	21
9	Concise approach to the aromatic yohimboid and protoberberine alkaloids via intramolecular Diels-Alder reactions 1988 ·Tetrahedron Letters ·Stephen F. Martin, Leo S. Geraci	6

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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