Herbert C. Murray

1.5k total citations
42 papers, 1.0k citations indexed

About

Herbert C. Murray is a scholar working on Molecular Biology, Organic Chemistry and Spectroscopy. According to data from OpenAlex, Herbert C. Murray has authored 42 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Molecular Biology, 12 papers in Organic Chemistry and 9 papers in Spectroscopy. Recurrent topics in Herbert C. Murray's work include Steroid Chemistry and Biochemistry (20 papers), Analytical Chemistry and Chromatography (9 papers) and Oxidative Organic Chemistry Reactions (7 papers). Herbert C. Murray is often cited by papers focused on Steroid Chemistry and Biochemistry (20 papers), Analytical Chemistry and Chromatography (9 papers) and Oxidative Organic Chemistry Reactions (7 papers). Herbert C. Murray collaborates with scholars based in United States. Herbert C. Murray's co-authors include D. H. Peterson, L. M. Reineke, P. Meister, S. H. Eppstein, Gunther S. Fonken, Adi Y. Weintraub, Roy A. Johnson, H. Marian Leigh, Milton E. Herr and Barney J. Magerlein 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

Herbert C. Murray

42 papers receiving 807 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Herbert C. Murray United States	18	747	219	209	130	119	42	1.0k
Ewart R. H. Jones United States	14	312 0.4×	122 0.6×	176 0.8×	54 0.4×	50 0.4×	79	588
John J. Partridge United States	17	325 0.4×	66 0.3×	402 1.9×	112 0.9×	71 0.6×	26	871
S. H. Eppstein United States	12	396 0.5×	96 0.4×	39 0.2×	58 0.4×	85 0.7×	18	491
Roger E. Beyler India	12	334 0.4×	34 0.2×	348 1.7×	63 0.5×	89 0.7×	22	698
Ronald L. Hanson United States	21	888 1.2×	174 0.8×	285 1.4×	93 0.7×	42 0.4×	52	1.2k
Robin B. Boar United Kingdom	14	403 0.5×	102 0.5×	255 1.2×	54 0.4×	23 0.2×	47	687
Philip W. Le Quesne United States	21	392 0.5×	329 1.5×	657 3.1×	38 0.3×	25 0.2×	65	1.2k
Robert R. Engle United States	6	287 0.4×	36 0.2×	270 1.3×	66 0.5×	41 0.3×	13	609
V. VanRheenen United States	4	358 0.5×	91 0.4×	780 3.7×	49 0.4×	23 0.2×	5	1000
J. F. McGhie United Kingdom	14	317 0.4×	84 0.4×	298 1.4×	72 0.6×	15 0.1×	50	636

Countries citing papers authored by Herbert C. Murray

Since Specialization

Citations

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

Fields of papers citing papers by Herbert C. Murray

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Herbert C. Murray. 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 Herbert C. Murray. The network helps show where Herbert C. Murray may publish in the future.

Co-authorship network of co-authors of Herbert C. Murray

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

All Works

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20 of 20 papers shown

Schneider, William P. & Herbert C. Murray. (1973). Microbiological reduction and resolution of prostaglandins. Synthesis of natural PGF2.alpha. and ENT-PGF2.beta. methyl esters. The Journal of Organic Chemistry. 38(2). 397–398. 14 indexed citations

Johnson, Roy A., Milton E. Herr, Herbert C. Murray, & L. M. Reineke. (1971). Stereochemistry of microbiological hydroxylation. VII. Influence of a methyl substitutent on the microbiological oxygenation of cyclic compounds. Journal of the American Chemical Society. 93(19). 4880–4883. 6 indexed citations

Johnson, Roy A. & Herbert C. Murray. (1971). Microbial hydroxylation of 1,2-(α-oxotetramethylene)ferrocene. Journal of the Chemical Society D Chemical Communications. 0(16). 989–990. 4 indexed citations

Johnson, Roy A., Herbert C. Murray, & L. M. Reineke. (1971). Stereochemistry of microbiological hydroxylation. VI. Microbiological oxygenation of acyclic N-alkylbenzamides. Journal of the American Chemical Society. 93(19). 4872–4880. 11 indexed citations

Herr, Milton E., et al.. (1970). Stereochemistry of microbiological hydroxylation. V. Optically active adamantanes via microbiological hydroxylation. Absolute configuration and the "anti-octant" effect of the axial 3-methyl group of cyclohexanone. The Journal of Organic Chemistry. 35(11). 3607–3611. 8 indexed citations

Johnson, Roy A., Milton E. Herr, Herbert C. Murray, & Gunther S. Fonken. (1970). Stereochemistry of microbiological hydroxylation. IV. Stereochemistry of the microbiological oxygenation of N-acylcyclohexylamines. The Journal of Organic Chemistry. 35(3). 622–626. 12 indexed citations

Johnson, Roy A., Herbert C. Murray, & L. M. Reineke. (1969). Stereochemistry of microbiological hydroxylation. III. Hydroxylation of 3-benzoyl-3-azabicyclo[3.3.1]nonane with Rhizopus arrhizus. Novel chromic acid oxidations of substrate and product. The Journal of Organic Chemistry. 34(12). 3834–3837. 4 indexed citations

Fonken, Gunther S., Milton E. Herr, Herbert C. Murray, & L. M. Reineke. (1967). Microbiological Hydroxylation of Monocyclic Alcohols. Journal of the American Chemical Society. 89(3). 672–675. 35 indexed citations

Fonken, Gunther S. & Herbert C. Murray. (1962). Microbiological Transformations of Steroids. XVII.¹ Dehydrogenation of 5β-Pregnane-3,-11,20-trione 20-Ethylene Ketal by Septomyxa affinis. The Journal of Organic Chemistry. 27(3). 1102–1104. 3 indexed citations

10.

Fonken, Gunther S., Herbert C. Murray, & L. M. Reineke. (1960). PATHWAY OF PROGESTERONE OXIDATION BY CLADOSPORIUM RESINAE. Journal of the American Chemical Society. 82(20). 5507–5508. 52 indexed citations

11.

Hanze, A. R., Oldrich K. Sebek, & Herbert C. Murray. (1960). Microbiological Transformations of Steroids. XVI. Multiple Oxidation of the Steroid Nucleus¹. The Journal of Organic Chemistry. 25(11). 1968–1971. 6 indexed citations

12.

Peterson, D. H., P. Meister, Adi Y. Weintraub, et al.. (1955). Microbiological Transformation of Steroids. XIII. Oxygenation of 16α, 17α-Oxidoprogesterone to 11α-Hydroxy-16α, 17α-oxidoprogesterone by Rhizopus Nigricans Ehrb. (A.T.C.C. 6227b)¹. Journal of the American Chemical Society. 77(16). 4428–4429. 17 indexed citations

13.

Eppstein, S. H., P. Meister, H. Marian Leigh, et al.. (1954). Microbiological Transformations of Steroids.¹ X. The Oxygenation of Androgens by Rhizopus². Journal of the American Chemical Society. 76(12). 3174–3179. 33 indexed citations

14.

Meister, P., D. H. Peterson, Herbert C. Murray, et al.. (1953). Microbiological Transformations of Steroids. V. The Oxygenation of 17α-Hydroxyprogesterone to 6β,17α-Dihydroxyprogesterone and 11α,17α-Dihydroxyprogesterone¹. Journal of the American Chemical Society. 75(2). 416–418. 15 indexed citations

15.

Peterson, D. H., P. Meister, S. H. Eppstein, et al.. (1953). Microbiological Transformations of Steroids. VI. Preparation of 11α-Hydroxy-6-dehydroprogesterone. Journal of the American Chemical Society. 75(2). 419–421. 11 indexed citations

16.

Peterson, D. H., S. H. Eppstein, P. Meister, et al.. (1953). MICROBIOLOGICAL TRANSFORMATIONS OF STEROIDS. IX. DEGRADATION OF C₂₁ STEROIDS TO C₁₉ KETONES AND TO TESTOLOLACTONE. Journal of the American Chemical Society. 75(22). 5768–5769. 59 indexed citations

17.

Meister, P., D. H. Peterson, Herbert C. Murray, et al.. (1953). Microbiological Transformations of Steroids. II. The Preparation of 11 α-Hydroxy- 17 α-progesterone. Journal of the American Chemical Society. 75(1). 55–57. 25 indexed citations

18.

Peterson, D. H., S. H. Eppstein, P. Meister, et al.. (1953). Microbiological Transformations of Steroids. IV. The 11-Epimer of Compound F and Other New Oxygenated Derivatives of Reichstein's Compound S. A New Route to Cortisone¹. Journal of the American Chemical Society. 75(2). 412–415. 35 indexed citations

19.

Peterson, D. H., Herbert C. Murray, S. H. Eppstein, et al.. (1952). Microbiological Transformations of Steroids.¹ I. Introduction of Oxygen at Carbon-11 of Progesterone. Journal of the American Chemical Society. 74(23). 5933–5936. 131 indexed citations

20.

Peterson, D. H. & Herbert C. Murray. (1952). MICROBIOLOGICAL OXYGENATION OF STEROIDS AT CARBON 11. Journal of the American Chemical Society. 74(7). 1871–1872. 129 indexed citations

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