Steven J. Wittenberger

1.9k total citations
32 papers, 1.5k citations indexed

About

Steven J. Wittenberger is a scholar working on Organic Chemistry, Molecular Biology and Pharmaceutical Science. According to data from OpenAlex, Steven J. Wittenberger has authored 32 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Organic Chemistry, 8 papers in Molecular Biology and 4 papers in Pharmaceutical Science. Recurrent topics in Steven J. Wittenberger's work include Chemical Synthesis and Analysis (5 papers), Synthetic Organic Chemistry Methods (5 papers) and Asymmetric Synthesis and Catalysis (5 papers). Steven J. Wittenberger is often cited by papers focused on Chemical Synthesis and Analysis (5 papers), Synthetic Organic Chemistry Methods (5 papers) and Asymmetric Synthesis and Catalysis (5 papers). Steven J. Wittenberger collaborates with scholars based in United States and United Kingdom. Steven J. Wittenberger's co-authors include Eric G. Moschetta, David M. Barnes, Steven A. King, Shailendra Bordawekar, Kaid C. Harper, Howard E. Morton, Jianguo Ji, Edwin Vedējs, David R. Hill and Maureen A. McLaughlin and has published in prestigious journals such as Journal of the American Chemical Society, The Journal of Organic Chemistry and Tetrahedron.

In The Last Decade

Steven J. Wittenberger

32 papers receiving 1.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Steven J. Wittenberger United States 17 1.3k 324 189 148 75 32 1.5k
Alba Díaz‐Rodríguez United Kingdom 18 621 0.5× 581 1.8× 198 1.0× 200 1.4× 109 1.5× 32 1.2k
Joseph D. Armstrong United States 23 1.3k 1.0× 595 1.8× 389 2.1× 176 1.2× 63 0.8× 40 1.7k
Lee T. Boulton United Kingdom 15 709 0.6× 512 1.6× 211 1.1× 78 0.5× 36 0.5× 22 889
Gerald A. Weisenburger United States 12 1.1k 0.8× 545 1.7× 271 1.4× 93 0.6× 53 0.7× 24 1.2k
Hideki Kurihara Japan 15 1.3k 1.0× 432 1.3× 235 1.2× 51 0.3× 171 2.3× 41 1.6k
Joseph P. A. Harrity United Kingdom 16 1.7k 1.4× 745 2.3× 206 1.1× 41 0.3× 52 0.7× 24 1.8k
Herbert F. Schuster United States 13 905 0.7× 452 1.4× 148 0.8× 58 0.4× 56 0.7× 23 1.4k
Valérie Bénéteau France 16 808 0.6× 254 0.8× 72 0.4× 58 0.4× 89 1.2× 40 967
Daniel Beaupère France 17 663 0.5× 407 1.3× 139 0.7× 48 0.3× 79 1.1× 77 853
Sushobhan Chowdhury India 19 1.7k 1.3× 314 1.0× 99 0.5× 39 0.3× 122 1.6× 56 1.8k

Countries citing papers authored by Steven J. Wittenberger

Since Specialization
Citations

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

Fields of papers citing papers by Steven J. Wittenberger

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Steven J. Wittenberger

This figure shows the co-authorship network connecting the top 25 collaborators of Steven J. Wittenberger. A scholar is included among the top collaborators of Steven J. Wittenberger 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 Steven J. Wittenberger. Steven J. Wittenberger 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.
Harper, Kaid C., Eric G. Moschetta, Shailendra Bordawekar, & Steven J. Wittenberger. (2019). A Laser Driven Flow Chemistry Platform for Scaling Photochemical Reactions with Visible Light. ACS Central Science. 5(1). 109–115. 156 indexed citations
2.
Moschetta, Eric G., et al.. (2017). Heuristics, Protocol, and Considerations for Flow Chemistry in Photoredox Catalysis. ChemPhotoChem. 1(12). 539–543. 15 indexed citations
3.
Li, Wenke, et al.. (2006). An Improved Synthesis of Pyran-3,5-dione:  Application to the Synthesis of ABT-598, a Potassium Channel Opener, via Hantzsch Reaction. The Journal of Organic Chemistry. 71(4). 1725–1727. 6 indexed citations
4.
Wittenberger, Steven J., et al.. (2005). A general synthesis of N-aryl- and N-alkyl-2-aminobenzoxazoles. Tetrahedron Letters. 46(48). 8341–8343. 32 indexed citations
5.
Leanna, M. Robert, Maureen A. McLaughlin, Francis A. J. Kerdesky, et al.. (2004). The synthesis of ketolide antibiotic ABT-773 (cethromycin). Tetrahedron. 60(45). 10171–10180. 35 indexed citations
6.
Barnes, David M., John A. DeMattei, David R. Hill, et al.. (2003). A highly diastereoselective vinylogous Mannich condensation and 1,4-conjugate addition of (Z)-propenyl cuprate in the synthesis of an influenza neuraminidase inhibitor. Tetrahedron Asymmetry. 14(22). 3541–3551. 30 indexed citations
7.
Barnes, David M., et al.. (2002). Synthesis of an Influenza Neuraminidase Inhibitor Intermediate via a Highly Diastereoselective Coupling Reaction. Organic Letters. 4(9). 1427–1430. 20 indexed citations
8.
Fernando, Dilinie P., Michael G. Fickes, Ashok K. Gupta, et al.. (2002). The Development of a Large-Scale Synthesis of Matrix Metalloproteinase Inhibitor, ABT-518. Organic Process Research & Development. 6(3). 329–335. 10 indexed citations
9.
Wittenberger, Steven J., et al.. (2002). An Efficient Scalable Process for the Synthesis of N-Boc-2-tert-butyldimethylsiloxypyrrole. Organic Process Research & Development. 6(4). 416–418. 5 indexed citations
10.
Hill, David R., et al.. (2001). 2,2,2-Trifluoroethyl Formate:  A Versatile and Selective Reagent for the Formylation of Alcohols, Amines, andN-Hydroxylamines. Organic Letters. 4(1). 111–113. 90 indexed citations
11.
Wittenberger, Steven J. & Maureen A. McLaughlin. (1999). Preparation of endothelin antagonist ABT-627. Tetrahedron Letters. 40(40). 7175–7178. 13 indexed citations
12.
Wittenberger, Steven J.. (1996). An Efficient Synthesis of the Cholinergic Channel Activator ABT-418. The Journal of Organic Chemistry. 61(1). 356–358. 27 indexed citations
13.
Wittenberger, Steven J., Steven A. Boyd, & William R. Baker. (1993). Diastereoselective Alkylations oft-Butyl Glycolate Ether Enolates. Synlett. 1993(10). 795–797. 4 indexed citations
14.
Kerdesky, Francis A. J., Anthony R. Haight, B. A. Narayanan, et al.. (1993). An Efficient Synthesis of an Angiotensin II Antagonist (A-81988). Synthetic Communications. 23(14). 2027–2039. 8 indexed citations
15.
Wittenberger, Steven J., et al.. (1993). 2-Butyl-4-iodoimidazole-5-carboxaldehyde: A Versatile Intermediate for the Synthesis of Highly Functionalized Imidazoles. Synthetic Communications. 23(22). 3231–3248. 6 indexed citations
17.
Falck, John R., et al.. (1990). Total synthesis of the 5-methylenephosphonate analogue of D-myo-inositol 1,4,5-trisphosphate. Journal of the Chemical Society Chemical Communications. 953–953. 32 indexed citations
18.
Falck, John R., et al.. (1990). Perkin communications. Heterocyclic [4++ 2] cycloadditions: the reactivity of pyridinium salts with electron-rich olefins. Journal of the Chemical Society Perkin Transactions 1. 413–413. 3 indexed citations
19.
Vedējs, Edwin, James D. Rodgers, & Steven J. Wittenberger. (1988). A sulfur-mediated total synthesis of Zygosporin E. Journal of the American Chemical Society. 110(14). 4822–4823. 25 indexed citations
20.
Vedējs, Edwin, James D. Rodgers, & Steven J. Wittenberger. (1988). A mild procedure for synthesis of the cytochalasin isoindolone; Allyl selenides from allyl silanes and PhSeSe+(CH3)Ph BF4−. Tetrahedron Letters. 29(19). 2287–2290. 2 indexed citations

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