Christopher J. Borths

2.5k total citations · 1 hit paper
17 papers, 2.0k citations indexed

About

Christopher J. Borths is a scholar working on Organic Chemistry, Molecular Biology and Health, Toxicology and Mutagenesis. According to data from OpenAlex, Christopher J. Borths has authored 17 papers receiving a total of 2.0k indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Organic Chemistry, 5 papers in Molecular Biology and 2 papers in Health, Toxicology and Mutagenesis. Recurrent topics in Christopher J. Borths's work include Asymmetric Synthesis and Catalysis (3 papers), Catalytic C–H Functionalization Methods (2 papers) and Catalytic Cross-Coupling Reactions (2 papers). Christopher J. Borths is often cited by papers focused on Asymmetric Synthesis and Catalysis (3 papers), Catalytic C–H Functionalization Methods (2 papers) and Catalytic Cross-Coupling Reactions (2 papers). Christopher J. Borths collaborates with scholars based in United States, United Kingdom and France. Christopher J. Borths's co-authors include David W. C. MacMillan, Kateri A. Ahrendt, Margaret M. Faul, Johann Chan, Robert D. Larsen, Kyle D. Baucom, Jinkun Huang, Ying Chen, Shawn D. Walker and Jacqueline C. S. Woo and has published in prestigious journals such as Journal of the American Chemical Society, Analytical Chemistry and Cancer Research.

In The Last Decade

Christopher J. Borths

17 papers receiving 2.0k citations

Hit Papers

New Strategies for Organic Catalysis:  The First Highly E... 2000 2026 2008 2017 2000 400 800 1.2k

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Christopher J. Borths United States 11 1.7k 448 386 120 118 17 2.0k
Victor I. Maleev Russia 29 1.5k 0.9× 978 2.2× 608 1.6× 181 1.5× 99 0.8× 117 2.2k
András Kotschy Hungary 24 1.2k 0.7× 144 0.3× 413 1.1× 55 0.5× 74 0.6× 88 1.6k
M. G. Finn United States 22 1.1k 0.7× 463 1.0× 204 0.5× 90 0.8× 151 1.3× 37 1.4k
Kelvin L. Billingsley United States 18 1.9k 1.1× 197 0.4× 309 0.8× 147 1.2× 81 0.7× 36 2.3k
Davide Audisio France 32 2.0k 1.2× 373 0.8× 785 2.0× 89 0.7× 260 2.2× 93 2.7k
Birgit Wibbeling Germany 33 3.0k 1.8× 1.3k 2.8× 308 0.8× 172 1.4× 146 1.2× 131 3.3k
Takuya Kurahashi Japan 36 3.4k 2.0× 573 1.3× 420 1.1× 122 1.0× 42 0.4× 119 3.6k
Henrik Gulyás Spain 24 1.8k 1.1× 695 1.6× 501 1.3× 31 0.3× 198 1.7× 39 1.9k
Tommy Bui United States 14 2.3k 1.3× 677 1.5× 650 1.7× 145 1.2× 58 0.5× 22 2.5k
Laura Palombi Italy 22 1.2k 0.7× 172 0.4× 203 0.5× 62 0.5× 35 0.3× 90 1.4k

Countries citing papers authored by Christopher J. Borths

Since Specialization
Citations

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

Fields of papers citing papers by Christopher J. Borths

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Christopher J. Borths

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

All Works

17 of 17 papers shown
1.
Borths, Christopher J., et al.. (2022). Nitrosamine Risk Assessments in Oligonucleotides. Organic Process Research & Development. 27(10). 1693–1702. 7 indexed citations
2.
Borths, Christopher J., Eric L. Elliott, Heewon Lee, et al.. (2021). Control of Mutagenic Impurities: Survey of Pharmaceutical Company Practices and a Proposed Framework for Industry Alignment. Organic Process Research & Development. 25(4). 831–837. 15 indexed citations
3.
Borths, Christopher J., Michael J. Burns, Timothy T. Curran, & Nathan D. Ide. (2021). Nitrosamine Reactivity: A Survey of Reactions and Purge Processes. Organic Process Research & Development. 25(8). 1788–1801. 21 indexed citations
4.
Borths, Christopher J. & Shawn D. Walker. (2020). Accelerating Pharmaceutical Development via Metal‐Mediated Bond Formation. Israel Journal of Chemistry. 60(3-4). 340–350. 5 indexed citations
5.
Achmatowicz, Michał, John G. Allen, Matthew M. Bio, et al.. (2016). Telescoped Process to Manufacture 6,6,6-Trifluorofucose via Diastereoselective Transfer Hydrogenation: Scalable Access to an Inhibitor of Fucosylation Utilized in Monoclonal Antibody Production. The Journal of Organic Chemistry. 81(11). 4736–4743. 8 indexed citations
6.
Hamblett, Kevin J., Allison P. Jacob, Jesse L. Gurgel, et al.. (2015). SLC46A3 Is Required to Transport Catabolites of Noncleavable Antibody Maytansine Conjugates from the Lysosome to the Cytoplasm. Cancer Research. 75(24). 5329–5340. 90 indexed citations
7.
Luo, Quanzhou, et al.. (2015). Structural Characterization of a Monoclonal Antibody–Maytansinoid Immunoconjugate. Analytical Chemistry. 88(1). 695–702. 50 indexed citations
8.
Kiang, Y.-H., Eric A. Bercot, Qiong Wu, et al.. (2015). Selection of a Suitable Physical Form and Development of a Crystallization Process for a PDE10A Inhibitor Exhibiting Enantiotropic Polymorphism. Organic Process Research & Development. 19(12). 1849–1858. 5 indexed citations
9.
Borths, Christopher J., Kyle D. Baucom, & Anil S. Guram. (2014). Effective Conversion of Heteroaromatic Ketones into Primary Amines via Hydrogenation of Intermediate Ketoximes. Synlett. 26(2). 201–204. 5 indexed citations
10.
Walker, Shawn D., Christopher J. Borths, Liang Huang, et al.. (2011). Development of a Scalable Synthesis of a GPR40 Receptor Agonist. Organic Process Research & Development. 15(3). 570–580. 41 indexed citations
11.
Huang, Jinkun, Johann Chan, Ying Chen, et al.. (2010). A Highly Efficient Palladium/Copper Cocatalytic System for Direct Arylation of Heteroarenes: An Unexpected Effect of Cu(Xantphos)I. Journal of the American Chemical Society. 132(11). 3674–3675. 294 indexed citations
12.
Borths, Christopher J., Johann Chan, Brenda J. Burke, & Robert D. Larsen. (2010). ChemInform Abstract: Synthesis of O‐Ethyl Thioformate: A Useful Reagent for the Thioformylation of Amines.. ChemInform. 41(15). 1 indexed citations
13.
Borths, Christopher J., Johann Chan, Brenda J. Burke, & Robert D. Larsen. (2009). Synthesis of O-Ethyl Thioformate: A Useful Reagent for the Thioformylation of Amines. Synlett. 2009(19). 3139–3142. 13 indexed citations
14.
Borths, Christopher J., Diane E. Carrera, & David W. C. MacMillan. (2009). Development of a general, enantioselective organocatalytic Mukaiyama–Michael reaction with α,β-unsaturated aldehydes. Tetrahedron. 65(33). 6746–6753. 31 indexed citations
15.
Cui, Sheng, Shawn D. Walker, Jacqueline C. S. Woo, et al.. (2009). Practical Asymmetric Conjugate Alkynylation of Meldrum’s Acid-Derived Acceptors: Access to Chiral β-Alkynyl Acids. Journal of the American Chemical Society. 132(2). 436–437. 41 indexed citations
16.
Woo, Jacqueline C. S., Shawn D. Walker, Jason S. Tedrow, et al.. (2007). Highly Selective Rhodium-Catalyzed Conjugate Addition Reactions of 4-Oxobutenamides. The Journal of Organic Chemistry. 72(23). 8870–8876. 40 indexed citations
17.
Ahrendt, Kateri A., Christopher J. Borths, & David W. C. MacMillan. (2000). New Strategies for Organic Catalysis:  The First Highly Enantioselective Organocatalytic Diels−Alder Reaction. Journal of the American Chemical Society. 122(17). 4243–4244. 1333 indexed citations breakdown →

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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