Todd G. Cochran

632 total citations
19 papers, 497 citations indexed

About

Todd G. Cochran is a scholar working on Molecular Biology, Organic Chemistry and Biomedical Engineering. According to data from OpenAlex, Todd G. Cochran has authored 19 papers receiving a total of 497 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 7 papers in Organic Chemistry and 5 papers in Biomedical Engineering. Recurrent topics in Todd G. Cochran's work include Biofuel production and bioconversion (4 papers), Analytical Chemistry and Chromatography (3 papers) and Cancer therapeutics and mechanisms (3 papers). Todd G. Cochran is often cited by papers focused on Biofuel production and bioconversion (4 papers), Analytical Chemistry and Chromatography (3 papers) and Cancer therapeutics and mechanisms (3 papers). Todd G. Cochran collaborates with scholars based in United States. Todd G. Cochran's co-authors include Fred Shafizadeh, Richard H. Furneaux, Yoshio Sakai, Jackson P. Scholl, Thomas T. Stevenson, Donald J. Abraham, Alain C. Huitric, R. D. Rosenstein, John V. St. Peter and Eli Shefter and has published in prestigious journals such as Journal of the American Chemical Society, Journal of Medicinal Chemistry and The Journal of Organic Chemistry.

In The Last Decade

Todd G. Cochran

19 papers receiving 481 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Todd G. Cochran United States 9 291 78 71 68 41 19 497
Herbert L. Hergert 13 157 0.5× 70 0.9× 107 1.5× 51 0.8× 27 0.7× 17 454
Eeva‐Liisa Tolppa Italy 11 197 0.7× 72 0.9× 45 0.6× 84 1.2× 29 0.7× 14 422
G. Tegge Germany 9 72 0.2× 20 0.3× 44 0.6× 25 0.4× 18 0.4× 96 360
Vincent G. Murphy United States 12 166 0.6× 59 0.8× 168 2.4× 23 0.3× 12 0.3× 29 475
С. А. Медведева Russia 10 71 0.2× 44 0.6× 91 1.3× 36 0.5× 22 0.5× 59 377
C. B. Purves Canada 12 132 0.5× 107 1.4× 109 1.5× 30 0.4× 16 0.4× 44 399
Mehmet Hakkı Alma Türkiye 10 128 0.4× 41 0.5× 85 1.2× 28 0.4× 47 1.1× 28 470
Barbara J. W. Cole United States 11 167 0.6× 17 0.2× 162 2.3× 91 1.3× 26 0.6× 22 438
Jiang Jian China 13 156 0.5× 19 0.2× 118 1.7× 19 0.3× 15 0.4× 40 445
M. Saska United States 10 110 0.4× 54 0.7× 56 0.8× 84 1.2× 68 1.7× 30 353

Countries citing papers authored by Todd G. Cochran

Since Specialization
Citations

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

Fields of papers citing papers by Todd G. Cochran

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Todd G. Cochran

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

All Works

19 of 19 papers shown
1.
Shafizadeh, Fred, et al.. (1984). The crystal structure of a septanose derived from levoglucosenone. Carbohydrate Research. 129. 55–61. 1 indexed citations
2.
Peter, John V. St. & Todd G. Cochran. (1982). Nitroglycerin loss from intravenous solutions administered with a volumetric infusion pump. American Journal of Health-System Pharmacy. 39(8). 1328–1330. 6 indexed citations
3.
Stevenson, Thomas T., Ronald E. Stenkamp, Lyle H. Jensen, et al.. (1981). The crystal structure of 1,5-anhydro-4-deoxy-d-glycero-hex-1-en-3-ulose. Carbohydrate Research. 90(2). 319–325. 9 indexed citations
4.
Cochran, Todd G., et al.. (1979). Application of pyrolytic methods for the saccharification of cellulose. 5 indexed citations
5.
Shafizadeh, Fred, Richard H. Furneaux, Todd G. Cochran, Jackson P. Scholl, & Yoshio Sakai. (1979). Production of levoglucosan and glucose from pyrolysis of cellulosic materials. Journal of Applied Polymer Science. 23(12). 3525–3539. 262 indexed citations
6.
Shafizadeh, Fred, Richard H. Furneaux, Thomas T. Stevenson, & Todd G. Cochran. (1978). Acid-catalyzed pyrolytic synthesis and decomposition of 1,4:3,6-dianhydro-α-d-glucopyranose. Carbohydrate Research. 61(1). 519–528. 53 indexed citations
7.
Shafizadeh, Fred, Richard H. Furneaux, Thomas T. Stevenson, & Todd G. Cochran. (1978). 1,5-Anhydro-4-deoxy-d-glycero-hex-1-en-3-ulose and other pyrolysis products of cellulose. Carbohydrate Research. 67(2). 433–447. 68 indexed citations
8.
Lo, Albert Y., Eli Shefter, & Todd G. Cochran. (1975). Analysis of N-Glycosyl Bond Length in Crystal Structures of Nucleosides and Nucleotides. Journal of Pharmaceutical Sciences. 64(10). 1707–1710. 9 indexed citations
9.
10.
Cochran, Todd G., et al.. (1975). 2,9β-Dimethyl-6,7-benzomorphan hydrochloride. Acta Crystallographica Section B. 31(3). 919–921. 2 indexed citations
11.
Parker, James M., et al.. (1974). Decomposition of Cannabidiol in Chloroform Solution. Journal of Pharmaceutical Sciences. 63(6). 970–971. 13 indexed citations
12.
Cochran, Todd G.. (1974). Stereochemistry and absolute configuration of the analgesic agonist-antagonist (-)-5-m-hydroxyphenyl-2-methylmorphan. Journal of Medicinal Chemistry. 17(9). 987–989. 9 indexed citations
13.
Cochran, Todd G., et al.. (1972). Stereochemistry and absolute configuration of the antibiotic spectinomycin: an X-ray diffraction study. Journal of the Chemical Society Chemical Communications. 494–494. 23 indexed citations
14.
Abraham, Donald J., Todd G. Cochran, & R. D. Rosenstein. (1971). Single-crystal x-ray structure of chemotherapeutic agents. V. Structures of 5-diazo-6-methoxy-6-hydrouracil and 2'-deoxy-5-diazo-6-hydro-065'-cyclouridine hemihydrate. Journal of the American Chemical Society. 93(23). 6279–6281. 11 indexed citations
15.
Abraham, Donald J., R. D. Rosenstein, Todd G. Cochran, Eldon E. Leutzinger, & L. B. TOWNSEND. (1971). Single crystal x-ray structure of chemotherapeutic agents IV, the structure of 6-chloro-9-(3,4-di--acetyl-2-deoxy-β-d-ribopyranosyl)purine. Tetrahedron Letters. 12(25). 2353–2356. 2 indexed citations
16.
Huitric, Alain C. & Todd G. Cochran. (1971). Nuclear magnetic resonance as a monitor in optical resolutions. II. Synthesis and resolution of cis- and trans-2-(o-bromophenyl)cyclohexylamines. The Journal of Organic Chemistry. 36(20). 3046–3048. 6 indexed citations
17.
Cochran, Todd G., et al.. (1970). Mechanism of the conversion of 2-nitrobenzyl systems into 2,1-benzisoxazoles. Journal of the Chemical Society C Organic. 2660–2660. 7 indexed citations
18.
19.
Cochran, Todd G., et al.. (1966). Application of the Haloalkoxy Reaction to 6-Nitroanthroxanic Acid1a. The Journal of Organic Chemistry. 31(4). 1303–1303. 4 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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