J.N. Marx

1.1k total citations
58 papers, 860 citations indexed

About

J.N. Marx is a scholar working on Organic Chemistry, Molecular Biology and Materials Chemistry. According to data from OpenAlex, J.N. Marx has authored 58 papers receiving a total of 860 indexed citations (citations by other indexed papers that have themselves been cited), including 33 papers in Organic Chemistry, 12 papers in Molecular Biology and 10 papers in Materials Chemistry. Recurrent topics in J.N. Marx's work include Radical Photochemical Reactions (10 papers), Oxidative Organic Chemistry Reactions (8 papers) and Synthetic Organic Chemistry Methods (8 papers). J.N. Marx is often cited by papers focused on Radical Photochemical Reactions (10 papers), Oxidative Organic Chemistry Reactions (8 papers) and Synthetic Organic Chemistry Methods (8 papers). J.N. Marx collaborates with scholars based in United States, Germany and Switzerland. J.N. Marx's co-authors include Lewis R. Norman, Purnendu Κ. Dasgupta, Vlastimil Kubáň, Emil H. White, Genfa Zhang, Albert W. Burgstahler, Darryl J. Bornhop, James H. Cox, Kenton H. Whitmire and Henry J. Shine and has published in prestigious journals such as Journal of the American Chemical Society, Journal of Applied Physics and Analytical Chemistry.

In The Last Decade

J.N. Marx

58 papers receiving 802 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
J.N. Marx United States 17 403 187 118 96 76 58 860
Christophe Morin France 17 509 1.3× 283 1.5× 67 0.6× 159 1.7× 89 1.2× 54 999
Yanyan Han China 15 381 0.9× 219 1.2× 124 1.1× 104 1.1× 67 0.9× 28 760
John Parrick United Kingdom 16 352 0.9× 212 1.1× 48 0.4× 137 1.4× 88 1.2× 49 743
Edwin G. E. Jahngen United States 16 535 1.3× 305 1.6× 81 0.7× 46 0.5× 66 0.9× 40 1.0k
Leonard S. Silbert United States 16 519 1.3× 158 0.8× 36 0.3× 78 0.8× 44 0.6× 42 779
A. D. Cross Poland 19 481 1.2× 331 1.8× 43 0.4× 123 1.3× 38 0.5× 62 1.2k
A. S. Lindsey United Kingdom 12 329 0.8× 142 0.8× 47 0.4× 127 1.3× 70 0.9× 36 794
Masato Tazaki Japan 20 126 0.3× 423 2.3× 115 1.0× 140 1.5× 135 1.8× 51 876
Antonio L. Zanocco Chile 18 416 1.0× 234 1.3× 64 0.5× 228 2.4× 124 1.6× 69 977
Y. Lion Belgium 12 257 0.6× 281 1.5× 86 0.7× 431 4.5× 235 3.1× 27 1.2k

Countries citing papers authored by J.N. Marx

Since Specialization
Citations

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

Fields of papers citing papers by J.N. Marx

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by J.N. Marx. 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 J.N. Marx. The network helps show where J.N. Marx may publish in the future.

Co-authorship network of co-authors of J.N. Marx

This figure shows the co-authorship network connecting the top 25 collaborators of J.N. Marx. A scholar is included among the top collaborators of J.N. Marx 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 J.N. Marx. J.N. Marx 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.
Marx, J.N. & Abdulaziz M. Ajlouni. (2010). Synthesis and Stereochemistry of Occidenol, a 4,5-Dihydro-Oxipin-Containing Sesquiterpene: A Pericyclic Approach. Natural Product Communications. 5(1). 5–8. 1 indexed citations
2.
Ochs, U., et al.. (2007). EBRA Migration Patterns of the Plasmacup with Ceramic or Polyethylene Inserts: A Randomised Study. Zeitschrift für Orthopädie und ihre Grenzgebiete. 145(S 1). S20–S24. 10 indexed citations
3.
Shine, Henry J., J.N. Marx, Anna T. Kelly, et al.. (2006). Addition of thianthrene cation radical to non-conjugated dienes—Part II: Addition to two double bonds. Journal of Sulfur Chemistry. 27(2). 139–147. 1 indexed citations
4.
5.
6.
Skwierawska, Anna, et al.. (2003). Rapid Removal of Benzyloxycarbonyl Groups from 1,4,7,10-Tetraazacyclododecane Derivatives by Catalytic Transfer Hydrogenation. Synthetic Communications. 33(3). 457–461. 2 indexed citations
7.
Skwierawska, Anna, et al.. (2001). Simple, high yielding synthesis of trifunctional fluorescent lanthanide chelates. Tetrahedron Letters. 42(23). 3823–3825. 15 indexed citations
8.
Marx, J.N., et al.. (1997). A stereoselective total synthesis of (−)-rishitin. Tetrahedron Letters. 38(11). 1889–1892. 12 indexed citations
9.
Dasgupta, Purnendu Κ., et al.. (1993). Spectrophotometric determination of H2O2 with 1-anilinonaphthalene-8-sulfonic acid and 4-aminoantipyrine with hematin as catalyst. Talanta. 40(7). 981–988. 7 indexed citations
10.
Kubáň, Vlastimil, Purnendu Κ. Dasgupta, & J.N. Marx. (1992). Nitroprusside and methylene blue methods for silicone membrane differentiated flow injection determination of sulfide in water and wastewater. Analytical Chemistry. 64(1). 36–43. 110 indexed citations
11.
Marx, J.N., et al.. (1987). Spirocyclic sesquiterpene synthesis via quinone methide coupling reactions. Anhydro-.beta.-rotunol. The Journal of Organic Chemistry. 52(3). 336–338. 8 indexed citations
12.
Marx, J.N.. (1983). A simple and convenient synthesis of β-haloketones. Tetrahedron. 39(9). 1529–1531. 14 indexed citations
13.
Marx, J.N.. (1975). A new synthesis of theaspirone, an odiferous principle of tea. Tetrahedron. 31(10). 1251–1253. 13 indexed citations
14.
Marx, J.N., et al.. (1975). Synthesis of some benzodipyrones, potential photochemical DNA crosslinking agents. Journal of Heterocyclic Chemistry. 12(2). 417–419. 16 indexed citations
15.
Marx, J.N., et al.. (1974). Migration of electronegative substituents. I. Relative migratory aptitude and migration tendency of the carbethoxy group in the dienone-phenol rearrangement. Journal of the American Chemical Society. 96(7). 2121–2129. 47 indexed citations
16.
Marx, J.N., James H. Cox, & Lewis R. Norman. (1972). 2-Carbomethoxycyclopent-2-enone. The Journal of Organic Chemistry. 37(26). 4489–4491. 31 indexed citations
17.
Marx, J.N.. (1970). An unusually stable salt from isophorone and hydrogen bromide. Tetrahedron Letters. 11(40). 3517–3520. 2 indexed citations
18.
Marx, J.N. & Emil H. White. (1969). The stereochemistry and synthesis of Achillin. Tetrahedron. 25(10). 2117–2120. 17 indexed citations
19.
Burgstahler, Albert W., J.N. Marx, & Duane F. Zinkel. (1969). Structure and stereochemistry of reduction products of abietictype resin acids. The Journal of Organic Chemistry. 34(6). 1550–1561. 19 indexed citations
20.
White, Emil H., Shoji Eguchi, & J.N. Marx. (1969). The synthesis and stereochemistry of desacetoxymatricarin and the stereochemistry of matricarin. Tetrahedron. 25(10). 2099–2115. 22 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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