Mark A. Huffman

3.8k total citations
47 papers, 2.2k citations indexed

About

Mark A. Huffman is a scholar working on Organic Chemistry, Molecular Biology and Inorganic Chemistry. According to data from OpenAlex, Mark A. Huffman has authored 47 papers receiving a total of 2.2k indexed citations (citations by other indexed papers that have themselves been cited), including 40 papers in Organic Chemistry, 18 papers in Molecular Biology and 11 papers in Inorganic Chemistry. Recurrent topics in Mark A. Huffman's work include Chemical Synthesis and Analysis (12 papers), Cyclopropane Reaction Mechanisms (11 papers) and Asymmetric Synthesis and Catalysis (10 papers). Mark A. Huffman is often cited by papers focused on Chemical Synthesis and Analysis (12 papers), Cyclopropane Reaction Mechanisms (11 papers) and Asymmetric Synthesis and Catalysis (10 papers). Mark A. Huffman collaborates with scholars based in United States, Japan and United Kingdom. Mark A. Huffman's co-authors include Lanny S. Liebeskind, Matthew M. Zhao, James M. McNamara, Jingjun Yin, Michael Shevlin, Nobuyoshi Yasuda, Rebecca T. Ruck, Ian W. Davies, Ian Mangion and Edward J. J. Grabowski and has published in prestigious journals such as Journal of the American Chemical Society, Angewandte Chemie International Edition and The Journal of Organic Chemistry.

In The Last Decade

Mark A. Huffman

47 papers receiving 2.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Mark A. Huffman United States 22 1.9k 406 387 147 75 47 2.2k
Zhijian Liu United States 27 2.2k 1.1× 519 1.3× 289 0.7× 103 0.7× 79 1.1× 51 2.7k
Nobuyoshi Yasuda United States 26 1.9k 1.0× 606 1.5× 458 1.2× 108 0.7× 97 1.3× 106 2.3k
Kyungsoo Oh South Korea 31 2.2k 1.1× 432 1.1× 403 1.0× 167 1.1× 114 1.5× 108 2.6k
Shigeki Sano Japan 22 1.3k 0.7× 510 1.3× 236 0.6× 193 1.3× 48 0.6× 122 1.6k
Yong Xia China 30 2.7k 1.4× 266 0.7× 322 0.8× 209 1.4× 31 0.4× 76 2.9k
Renhua Fan China 30 2.9k 1.5× 410 1.0× 314 0.8× 105 0.7× 42 0.6× 101 3.1k
Yasuo Kikugawa Japan 21 1.6k 0.8× 469 1.2× 267 0.7× 205 1.4× 41 0.5× 101 1.8k
Arianna Quintavalla Italy 23 997 0.5× 398 1.0× 142 0.4× 59 0.4× 160 2.1× 69 1.4k
Mahavir Prashad Switzerland 23 1.2k 0.6× 466 1.1× 333 0.9× 76 0.5× 98 1.3× 88 1.6k
J. Craig Ruble United States 21 1.9k 1.0× 617 1.5× 804 2.1× 79 0.5× 87 1.2× 35 2.1k

Countries citing papers authored by Mark A. Huffman

Since Specialization
Citations

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

Fields of papers citing papers by Mark A. Huffman

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Mark A. Huffman. 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 Mark A. Huffman. The network helps show where Mark A. Huffman may publish in the future.

Co-authorship network of co-authors of Mark A. Huffman

This figure shows the co-authorship network connecting the top 25 collaborators of Mark A. Huffman. A scholar is included among the top collaborators of Mark A. Huffman 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 Mark A. Huffman. Mark A. Huffman 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.
Johnson, Heather C., Shaoguang Zhang, Anna Fryszkowska, et al.. (2021). Biocatalytic oxidation of alcohols using galactose oxidase and a manganese(iii) activator for the synthesis of islatravir. Organic & Biomolecular Chemistry. 19(7). 1620–1625. 18 indexed citations
2.
Kim, Taejin, Chen Zhang, David Rozzell, et al.. (2019). Hemoprotein‐Catalyzed Cyclopropanation En Route to the Chiral Cyclopropanol Fragment of Grazoprevir. ChemBioChem. 20(9). 1129–1132. 13 indexed citations
3.
Chobanian, Harry R., Barbara Pio, Yan Guo, et al.. (2015). Improved Stability of Proline-Derived Direct Thrombin Inhibitors through Hydroxyl to Heterocycle Replacement. ACS Medicinal Chemistry Letters. 6(5). 553–557. 6 indexed citations
4.
Ruck, Rebecca T., Mark A. Huffman, Gavin W. Stewart, et al.. (2012). Route Development and Multikilogram GMP Delivery of a Somatostatin Receptor Antagonist. Organic Process Research & Development. 16(8). 1329–1337. 8 indexed citations
5.
Mangion, Ian, Rebecca T. Ruck, Nelo R. Rivera, Mark A. Huffman, & Michael Shevlin. (2011). A Concise Synthesis of a β-Lactamase Inhibitor. Organic Letters. 13(20). 5480–5483. 102 indexed citations
6.
Mangion, Ian, et al.. (2009). Iridium-Catalyzed X−H Insertions of Sulfoxonium Ylides. Organic Letters. 11(16). 3566–3569. 156 indexed citations
7.
Ruck, Rebecca T., Mark A. Huffman, Mary M. Kim, et al.. (2008). Palladium‐Catalyzed Tandem Heck Reaction/CH Functionalization—Preparation of Spiro‐Indane‐Oxindoles. Angewandte Chemie International Edition. 47(25). 4711–4714. 164 indexed citations
8.
Kim, Mary M., Rebecca T. Ruck, Dalian Zhao, & Mark A. Huffman. (2008). Green iodination of pyrazoles with iodine/hydrogen peroxide in water. Tetrahedron Letters. 49(25). 4026–4028. 42 indexed citations
9.
Huffman, Mark A., Jonathan D. Rosen, Roger N. Farr, & Joseph E. Lynch. (2007). Synthesis of a selective estrogen receptor β-modulator via asymmetric phase-transfer catalysis. Tetrahedron. 63(21). 4459–4463. 8 indexed citations
10.
Nelson, Todd D., Christopher J. Welch, Jonathan D. Rosen, et al.. (2004). Effective use of preparative chiral HPLC in a preclinical drug synthesis. Chirality. 16(9). 609–613. 20 indexed citations
11.
Nelson, Todd D., Jonathan D. Rosen, Jacqueline H. Smitrovich, et al.. (2004). Synthesis of a Potent hNK-1 Receptor Antagonist via an SN2 Reaction of an Enantiomerically Pure α-Alkoxy Sulfonate. Organic Letters. 7(1). 55–58. 17 indexed citations
12.
Nelson, Todd D., et al.. (2004). Syntheses of morpholine-2,3-diones and 2-hydroxymorpholin-3-ones: intermediates in the synthesis of aprepitant. Tetrahedron Letters. 45(48). 8917–8920. 13 indexed citations
13.
Yin, Jingjun, Devin S. Zarkowsky, David W. Thomas, Matthew M. Zhao, & Mark A. Huffman. (2004). Direct and Convenient Conversion of Alcohols to Fluorides. Organic Letters. 6(9). 1465–1468. 81 indexed citations
14.
Payack, Joseph F., Mark A. Huffman, Dongwei Cai, et al.. (2004). Dimethyltitanocene:  From Millimole to Kilomole. Organic Process Research & Development. 8(2). 256–259. 19 indexed citations
15.
Yin, Jingjun, Matthew M. Zhao, Mark A. Huffman, & James M. McNamara. (2003). Pd‐Catalyzed N‐Arylation of Heteroarylamines.. ChemInform. 34(11). 151 indexed citations
16.
Smitrovich, Jacqueline H., Chuanxing Qu, Lisa DiMichele, et al.. (2002). Pseudoephedrine as a Chiral Auxiliary for Asymmetric Michael Reactions:  Synthesis of 3-Aryl-δ-lactones. Organic Letters. 4(11). 1963–1966. 29 indexed citations
17.
Vailaya, Anant, et al.. (2001). Quantitative analysis of dimethyl titanocene by iodometric titration, gas chromatography and NMR. Journal of Pharmaceutical and Biomedical Analysis. 25(3-4). 577–588. 4 indexed citations
18.
Yasuda, Nobuyoshi, Mark A. Huffman, Lyndon C. Xavier, et al.. (1998). Practical Synthesis of Anti-Methicillin-Resistant Staphylococcus Aureus (MRSA) Carbapenem L-742,728. The Journal of Organic Chemistry. 63(16). 5438–5446. 24 indexed citations
19.
Huffman, Mark A., Lanny S. Liebeskind, & William T. Pennington. (1992). Reaction of cyclobutenones with low-valent metal reagents to form .eta.4- and .eta.2-vinylketene complexes. Reaction of .eta.4-vinylketene complexes with alkynes to form phenols. Organometallics. 11(1). 255–266. 97 indexed citations
20.
Boese, Roland, Mark A. Huffman, & K. Peter C. Vollhardt. (1991). Unique Reactivity of Heterodinuclear Pentacarbonyl(fulvalene)molybdenumruthenium with Alkynes: Fluxionality, Rearrangements, Structures, and First Reversible Conversion of a “Side‐on”‐ to a Semi‐Bridging Alkenylidene Ligand. Angewandte Chemie International Edition in English. 30(11). 1463–1465. 19 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Zhijian Liu Breakdown of academic impact, for papers by Nobuyoshi Yasuda Breakdown of academic impact, for papers by Kyungsoo Oh Breakdown of academic impact, for papers by Shigeki Sano Breakdown of academic impact, for papers by Yong Xia Breakdown of academic impact, for papers by Renhua Fan Breakdown of academic impact, for papers by Yasuo Kikugawa Breakdown of academic impact, for papers by Arianna Quintavalla Breakdown of academic impact, for papers by Mahavir Prashad Breakdown of academic impact, for papers by J. Craig Ruble
Rankless by CCL
2026