Roger E. Beyler

970 total citations · 1 hit paper
22 papers, 698 citations indexed

About

Roger E. Beyler is a scholar working on Molecular Biology, Genetics and Organic Chemistry. According to data from OpenAlex, Roger E. Beyler has authored 22 papers receiving a total of 698 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 8 papers in Genetics and 7 papers in Organic Chemistry. Recurrent topics in Roger E. Beyler's work include Steroid Chemistry and Biochemistry (16 papers), Estrogen and related hormone effects (8 papers) and Marine Sponges and Natural Products (4 papers). Roger E. Beyler is often cited by papers focused on Steroid Chemistry and Biochemistry (16 papers), Estrogen and related hormone effects (8 papers) and Marine Sponges and Natural Products (4 papers). Roger E. Beyler collaborates with scholars based in India and United States. Roger E. Beyler's co-authors include Lewis H. Sarett, George I. Poos, Glen E. Arth, William F. Johns, Max Tishler, Robert M. Moriarty, Ralph Hirschmann, Guy Ourisson, F Schneider and Randall R. Miller and has published in prestigious journals such as Journal of the American Chemical Society, The Journal of Organic Chemistry and Tetrahedron Letters.

In The Last Decade

Roger E. Beyler

21 papers receiving 580 citations

Hit Papers

Approaches to the Total Synthesis of Adrenal Steroids.1 V... 1953 2026 1977 2001 1953 100 200 300 400

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Roger E. Beyler India 12 348 334 89 89 63 22 698
Glen E. Arth United States 14 388 1.1× 412 1.2× 197 2.2× 142 1.6× 74 1.2× 25 922
E. B. Hershberg United States 17 230 0.7× 580 1.7× 153 1.7× 158 1.8× 83 1.3× 64 874
John J. Partridge United States 17 402 1.2× 325 1.0× 71 0.8× 86 1.0× 112 1.8× 26 871
Eugene P. Oliveto United States 20 535 1.5× 566 1.7× 114 1.3× 175 2.0× 106 1.7× 89 1.1k
G. Anner Switzerland 23 419 1.2× 683 2.0× 150 1.7× 302 3.4× 86 1.4× 44 1.0k
Ch. Meystre Switzerland 16 194 0.6× 463 1.4× 113 1.3× 172 1.9× 56 0.9× 22 641
Henry Laurent Australia 15 452 1.3× 294 0.9× 126 1.4× 160 1.8× 55 0.9× 76 804
N. L. Wendler United States 18 603 1.7× 561 1.7× 51 0.6× 124 1.4× 94 1.5× 103 1.1k
William F. Johns 13 202 0.6× 208 0.6× 38 0.4× 76 0.9× 47 0.7× 32 402
G. Forrest Woods United States 10 197 0.6× 225 0.7× 65 0.7× 58 0.7× 33 0.5× 40 527

Countries citing papers authored by Roger E. Beyler

Since Specialization
Citations

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

Fields of papers citing papers by Roger E. Beyler

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Roger E. Beyler. 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 Roger E. Beyler. The network helps show where Roger E. Beyler may publish in the future.

Co-authorship network of co-authors of Roger E. Beyler

This figure shows the co-authorship network connecting the top 25 collaborators of Roger E. Beyler. A scholar is included among the top collaborators of Roger E. Beyler 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 Roger E. Beyler. Roger E. Beyler 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.
Schneider, F, et al.. (1966). Steroidal alkylating agents I. Some 16-substituted androstanes and pregnanes. Steroids. 8(4). 553–563. 12 indexed citations
2.
Beyler, Roger E., et al.. (1965). The structure, stereochemistry and conformation of acacic acid. Tetrahedron Letters. 6(17). 1187–1197. 3 indexed citations
3.
Beyler, Roger E. & Guy Ourisson. (1965). ι-Acetyllongifolene1. The Journal of Organic Chemistry. 30(8). 2838–2839. 7 indexed citations
4.
Beyler, Roger E., et al.. (1961). 17,20;20,21-Bismethylenedioxy Steroids. V. A General Method for Protecting the Dihydroxyacetone Side Chain1. The Journal of Organic Chemistry. 26(7). 2421–2425. 15 indexed citations
5.
Beyler, Roger E., et al.. (1961). Bismethylenedioxy Steroids. VI. Synthesis of 9α-Methylhydrocortisone and 9α-Methylprednisolone1,2. The Journal of Organic Chemistry. 26(7). 2426–2431. 3 indexed citations
6.
Beyler, Roger E., et al.. (1960). Bismethylenedioxy Steroids. IV.1 11α-Methylhydrocortisone Acetate and 9α-Chloro-11α-Methylhydrocortisone Acetate. Journal of the American Chemical Society. 82(1). 178–182. 7 indexed citations
7.
Beyler, Roger E., et al.. (1960). Bismethylenedioxy Steroids. III. The Synthesis of 7α- and 7β-Methylhydrocortisones1. Journal of the American Chemical Society. 82(1). 170–178. 11 indexed citations
8.
Beyler, Roger E.. (1960). Some recent advances in the field of steroids. Journal of Chemical Education. 37(9). 491–491. 1 indexed citations
9.
Beyler, Roger E., et al.. (1959). Notes: Synthesis of 1,4-Pregnadiene-17α,20α,21-triol-3,11-dione. The Journal of Organic Chemistry. 24(9). 1386–1387. 5 indexed citations
10.
Beyler, Roger E., et al.. (1958). BISMETHYLENEDIOXY STEROIDS. II. SYNTHESIS OF 9α-METHYLHYDROCORTISONE AND 9α-METHYLPREDNISOLONE1. Journal of the American Chemical Society. 80(19). 5322–5323. 12 indexed citations
11.
Beyler, Roger E., et al.. (1958). 17,20;20,21-BISMETHYLENEDIOXY STEROIDS. Journal of the American Chemical Society. 80(6). 1517–1518. 15 indexed citations
12.
Beyler, Roger E., et al.. (1957). Identification and Synthesis of 4,17-Pregnadien-20-ol-21-al-3,11-dione Acetate1. Journal of the American Chemical Society. 79(19). 5297–5300. 14 indexed citations
13.
Beyler, Roger E., et al.. (1956). Synthesis of 16β-Chlorocortisone Acetate and Related 16-Substituted Steroids. The Journal of Organic Chemistry. 21(5). 572–574. 5 indexed citations
14.
Hirschmann, Ralph, Randall R. Miller, Roger E. Beyler, Lewis H. Sarett, & Max Tishler. (1955). A NEW BIOLOGICALLY POTENT STEROID: 1-DEHYDRO-9α-FLUOROHYDROCORTISONE ACETATE. Journal of the American Chemical Society. 77(11). 3166–3167. 20 indexed citations
15.
16.
Johns, William F., et al.. (1953). Approaches to the Total Synthesis of Adrenal Steroids. VII. A New Method for the Attachment of Ring D. Part A. Journal of the American Chemical Society. 75(9). 2112–2118. 50 indexed citations
17.
Poos, George I., Glen E. Arth, Roger E. Beyler, & Lewis H. Sarett. (1953). Approaches to the Total Synthesis of Adrenal Steroids.1 V. 4b-Methyl-7- ethylenedioxy-1,2,3,4,4aα,4b,5,6,7,8,10,10a β-dodecahydrophenanthrene-4 β-ol-1-one and Related Tricyclic Derivatives. Journal of the American Chemical Society. 75(2). 422–429. 412 indexed citations breakdown →
18.
Sarett, Lewis H., et al.. (1952). Approaches to Total Synthesis of Adrenal Steroids. I. 3-Ethoxy-1,3-pentadiene. Journal of the American Chemical Society. 74(6). 1393–1397. 19 indexed citations
19.
Beyler, Roger E. & Lewis H. Sarett. (1952). Approaches to Total Synthesis of Adrenal Steroids. II. 2,5- and 3,5-Dicarbomethoxy-5-methylcyclohexene-1,4-dione as Dienophiles. Journal of the American Chemical Society. 74(6). 1397–1401. 9 indexed citations
20.
Sarett, Lewis H., et al.. (1952). STEREOSPECIFIC TOTAL SYNTHESIS OF CORTISONE. Journal of the American Chemical Society. 74(19). 4974–4976. 41 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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