Janice E. Sieser

736 total citations
16 papers, 574 citations indexed

About

Janice E. Sieser is a scholar working on Organic Chemistry, Molecular Biology and Oncology. According to data from OpenAlex, Janice E. Sieser has authored 16 papers receiving a total of 574 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Organic Chemistry, 8 papers in Molecular Biology and 2 papers in Oncology. Recurrent topics in Janice E. Sieser's work include Chemical Synthesis and Analysis (8 papers), Catalytic Cross-Coupling Reactions (5 papers) and Catalytic C–H Functionalization Methods (3 papers). Janice E. Sieser is often cited by papers focused on Chemical Synthesis and Analysis (8 papers), Catalytic Cross-Coupling Reactions (5 papers) and Catalytic C–H Functionalization Methods (3 papers). Janice E. Sieser collaborates with scholars based in United States and United Kingdom. Janice E. Sieser's co-authors include Robert A. Singer, Stéphane Caron, Nga M., Martin A. Berliner, Arun K. Ghosh, Enrique Vázquez, Weiling Cai, Gregory W. Sluggett, Rajappa Vaidyanathan and Mélina Girardin and has published in prestigious journals such as Chemical Communications, The Journal of Organic Chemistry and Organic Letters.

In The Last Decade

Janice E. Sieser

16 papers receiving 560 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Janice E. Sieser United States 12 520 102 100 80 26 16 574
Shengfei Jin United States 15 643 1.2× 82 0.8× 74 0.7× 63 0.8× 29 1.1× 23 709
Deidre L. Sandrock United States 10 785 1.5× 96 0.9× 114 1.1× 49 0.6× 21 0.8× 11 832
Anne‐Marie Dechert‐Schmitt United States 10 537 1.0× 128 1.3× 86 0.9× 42 0.5× 18 0.7× 13 584
Matthew M. Zhao United States 11 449 0.9× 71 0.7× 168 1.7× 77 1.0× 23 0.9× 15 554
Kathleen J. Berger United States 6 399 0.8× 93 0.9× 105 1.1× 52 0.7× 20 0.8× 6 482
Jacob A. Kautzky United States 4 290 0.6× 79 0.8× 69 0.7× 95 1.2× 31 1.2× 4 395
Andriy V. Tymtsunik Ukraine 12 360 0.7× 68 0.7× 92 0.9× 74 0.9× 18 0.7× 26 397
Nils Frank Germany 7 826 1.6× 95 0.9× 75 0.8× 131 1.6× 26 1.0× 13 909
Mark W. Bundesmann United States 12 567 1.1× 58 0.6× 116 1.2× 63 0.8× 23 0.9× 15 661
Hans‐Ulrich Reißig Germany 16 519 1.0× 43 0.4× 70 0.7× 70 0.9× 42 1.6× 23 574

Countries citing papers authored by Janice E. Sieser

Since Specialization
Citations

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

Fields of papers citing papers by Janice E. Sieser

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Janice E. Sieser. 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 Janice E. Sieser. The network helps show where Janice E. Sieser may publish in the future.

Co-authorship network of co-authors of Janice E. Sieser

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

All Works

16 of 16 papers shown
1.
Sieser, Janice E., Mark T. Maloney, Steven J. Brenek, et al.. (2018). Ir-Catalyzed Borylation as an Efficient Route to a Nicotine Hapten. Organic Process Research & Development. 22(4). 527–534. 14 indexed citations
2.
Damon, David B., Kyle R. Leeman, Janice E. Sieser, et al.. (2015). Development of the Commercial Route for the Manufacture of a 5-Lipoxygenase Inhibitor PF-04191834. Organic Process Research & Development. 19(12). 1944–1953. 12 indexed citations
3.
Peng, Zhihui, John A. Ragan, Eric M. Cordi, et al.. (2013). Synthesis of Filibuvir. Part II. Second-Generation Synthesis of a 6,6-Disubstituted 2H-Pyranone via Dieckmann Cyclization of a β-Acetoxy Ester. Organic Process Research & Development. 18(1). 36–44. 7 indexed citations
4.
Lillie, Brett M., Robert W. McLaughlin, Charles W. Palmer, et al.. (2013). Development of an Efficient Pd-Catalyzed Coupling Process for Axitinib. Organic Process Research & Development. 18(1). 266–274. 48 indexed citations
5.
Singer, Robert A., John A. Ragan, Paul Bowles, et al.. (2013). Synthesis of Filibuvir. Part I. Diastereoselective Preparation of a β-Hydroxy Alkynyl Oxazolidinone and Conversion to a 6,6-Disubstituted 2H-Pyranone. Organic Process Research & Development. 18(1). 26–35. 19 indexed citations
6.
Sieser, Janice E., et al.. (2011). Synthesis of a Bicyclic Piperazine froml-Aspartic Acid and Application of a Fluoride-Promoted SNAr Coupling. Organic Process Research & Development. 15(6). 1328–1335. 5 indexed citations
7.
Caron, Stéphane, et al.. (2009). Preparation of a Corticotropin-Releasing Factor Antagonist by Nucleophilic Aromatic Substitution and Copper-Mediated Ether Formation. Organic Process Research & Development. 13(2). 324–330. 15 indexed citations
8.
Singer, Robert A., et al.. (2008). Streamlined Synthesis of the Bippyphos Family of Ligands and Cross-Coupling Applications. Organic Process Research & Development. 12(3). 480–489. 90 indexed citations
9.
Caron, Stéphane, et al.. (2007). Process Research and Development of an NK-1 Receptor Antagonist. Enantioselective Trifluoromethyl Addition to a Ketone in the Preparation of a Chiral Isochroman. Organic Process Research & Development. 11(6). 1015–1024. 72 indexed citations
10.
Singer, Robert A., et al.. (2006). Development of nonproprietary phosphine ligands for the Pd-catalyzed amination reaction. Tetrahedron Letters. 47(22). 3727–3731. 123 indexed citations
11.
Andresen, Brian M., John L. Tucker, Janice E. Sieser, et al.. (2006). Process Research and Scale-up of the κ-Opioid Receptor Agonist CJ-15,161 Drug Candidate. CHIMIA International Journal for Chemistry. 60(9). 554–554. 4 indexed citations
12.
Ghosh, Arun K., et al.. (2005). Cu-Catalyzed N-Arylation of Oxazolidinones:  An Efficient Synthesis of the κ-Opioid Receptor Agonist CJ-15161. The Journal of Organic Chemistry. 71(3). 1258–1261. 28 indexed citations
13.
Ghosh, Arun K., et al.. (2003). Palladium-Catalyzed Synthesis of N-Aryloxazolidinones from Aryl Chlorides. Organic Letters. 5(13). 2207–2210. 50 indexed citations
14.
Ghosh, Arun K., Janice E. Sieser, Stéphane Caron, & Timothy Watson. (2002). Synthesis of the kappa-agonist CJ-15,161 via a palladium-catalyzed cross-coupling reaction. Chemical Communications. 1644–1645. 13 indexed citations
15.
Caron, Stéphane, Nga M., & Janice E. Sieser. (2000). A practical, efficient, and rapid method for the oxidation of electron deficient pyridines using trifluoroacetic anhydride and hydrogen peroxide–urea complex. Tetrahedron Letters. 41(14). 2299–2302. 70 indexed citations
16.
BRAISH, T. F., Joel M. Hawkins, Timothy Norris, et al.. (2000). Construction of the (1α,5α,6α)-6-Amino-3-azabicyclo[3.1.0]hexane Ring System. Synlett. 1996(11). 1100–1102. 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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