Mark R. Biscoe

3.2k total citations
35 papers, 2.7k citations indexed

About

Mark R. Biscoe is a scholar working on Organic Chemistry, Inorganic Chemistry and Molecular Biology. According to data from OpenAlex, Mark R. Biscoe has authored 35 papers receiving a total of 2.7k indexed citations (citations by other indexed papers that have themselves been cited), including 33 papers in Organic Chemistry, 11 papers in Inorganic Chemistry and 5 papers in Molecular Biology. Recurrent topics in Mark R. Biscoe's work include Catalytic Cross-Coupling Reactions (26 papers), Catalytic C–H Functionalization Methods (22 papers) and Asymmetric Hydrogenation and Catalysis (10 papers). Mark R. Biscoe is often cited by papers focused on Catalytic Cross-Coupling Reactions (26 papers), Catalytic C–H Functionalization Methods (22 papers) and Asymmetric Hydrogenation and Catalysis (10 papers). Mark R. Biscoe collaborates with scholars based in United States. Mark R. Biscoe's co-authors include Stephen L. Buchwald, Brett P. Fors, Timothy E. Barder, Amruta Joshi‐Pangu, Chaoyuan Wang, Donald A. Watson, Ling Li, Shibin Zhao, Takashi Ikawa and Joseph Derosa and has published in prestigious journals such as Science, Journal of the American Chemical Society and Angewandte Chemie International Edition.

In The Last Decade

Mark R. Biscoe

34 papers receiving 2.6k 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 R. Biscoe United States 20 2.5k 596 291 166 144 35 2.7k
Shashank Shekhar United States 19 1.8k 0.7× 630 1.1× 284 1.0× 104 0.6× 97 0.7× 34 1.9k
Elena Buñuel Spain 26 3.3k 1.4× 693 1.2× 297 1.0× 172 1.0× 162 1.1× 78 3.7k
Brett P. Fors United States 15 2.0k 0.8× 469 0.8× 328 1.1× 104 0.6× 131 0.9× 17 2.2k
James P. Stambuli United States 25 3.6k 1.5× 747 1.3× 391 1.3× 125 0.8× 156 1.1× 39 3.8k
Paula Ruiz‐Castillo United States 4 2.3k 1.0× 594 1.0× 291 1.0× 91 0.5× 227 1.6× 5 2.6k
Matthew R. Netherton United States 16 2.2k 0.9× 533 0.9× 195 0.7× 133 0.8× 177 1.2× 27 2.4k
Yudao Ma China 29 2.2k 0.9× 433 0.7× 353 1.2× 158 1.0× 263 1.8× 73 2.4k
Hun Young Kim South Korea 27 2.0k 0.8× 386 0.6× 221 0.8× 116 0.7× 76 0.5× 80 2.1k
Haohua Huo China 21 2.2k 0.9× 638 1.1× 144 0.5× 186 1.1× 154 1.1× 37 2.4k
Tom G. Driver United States 38 4.5k 1.8× 1.0k 1.7× 457 1.6× 150 0.9× 126 0.9× 76 4.7k

Countries citing papers authored by Mark R. Biscoe

Since Specialization
Citations

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

Fields of papers citing papers by Mark R. Biscoe

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mark R. Biscoe

This figure shows the co-authorship network connecting the top 25 collaborators of Mark R. Biscoe. A scholar is included among the top collaborators of Mark R. Biscoe 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 R. Biscoe. Mark R. Biscoe 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.
Nafie, Jordan, et al.. (2025). Synthetic, Computational, and Experimental Studies of a Class 3 Atropisomeric α-Naphthyl Tropone. The Journal of Organic Chemistry. 90(32). 11501–11509.
2.
Ma, Xinghua, et al.. (2023). A general approach to stereospecific Pd-catalyzed cross-coupling reactions of benzylic stereocenters. Chemical Science. 14(48). 14124–14130. 1 indexed citations
3.
Ma, Xinghua, et al.. (2020). A General Approach to Stereospecific Cross-Coupling Reactions of Nitrogen-Containing Stereocenters. Chem. 6(3). 781–791. 16 indexed citations
4.
Ma, Xinghua, et al.. (2020). Stereoselectivity in Pd-catalysed cross-coupling reactions of enantioenriched nucleophiles. Nature Reviews Chemistry. 4(11). 584–599. 63 indexed citations
5.
6.
Zhao, Shibin, et al.. (2018). Enantiodivergent Pd-catalyzed C–C bond formation enabled through ligand parameterization. Science. 362(6415). 670–674. 154 indexed citations
7.
Derosa, Joseph, et al.. (2016). Stereospecific Palladium‐Catalyzed Acylation of Enantioenriched Alkylcarbastannatranes: A General Alternative to Asymmetric Enolate Reactions. Angewandte Chemie International Edition. 56(3). 856–860. 32 indexed citations
8.
9.
Li, Ling, Chaoyuan Wang, R. L. Huang, & Mark R. Biscoe. (2013). Stereoretentive Pd-catalysed Stille cross-coupling reactions of secondary alkyl azastannatranes and aryl halides. Nature Chemistry. 5(7). 607–612. 148 indexed citations
10.
Biscoe, Mark R. & Amruta Joshi‐Pangu. (2012). The Use of Tertiary Alkylmagnesium Nucleophiles in Ni-Catalyzed Cross-Coupling Reactions. Synlett. 23(8). 1103–1107. 16 indexed citations
11.
Joshi‐Pangu, Amruta, et al.. (2012). Palladium-Catalyzed Borylation of Primary Alkyl Bromides. The Journal of Organic Chemistry. 77(15). 6629–6633. 70 indexed citations
12.
Joshi‐Pangu, Amruta, Chaoyuan Wang, & Mark R. Biscoe. (2011). Nickel-Catalyzed Kumada Cross-Coupling Reactions of Tertiary Alkylmagnesium Halides and Aryl Bromides/Triflates. Journal of the American Chemical Society. 133(22). 8478–8481. 153 indexed citations
13.
Joshi‐Pangu, Amruta, Madhu Ganesh, & Mark R. Biscoe. (2011). Nickel-Catalyzed Negishi Cross-Coupling Reactions of Secondary Alkylzinc Halides and Aryl Iodides. Organic Letters. 13(5). 1218–1221. 83 indexed citations
14.
Biscoe, Mark R., et al.. (2009). Simple, efficient protocols for the Pd-catalyzed cross-coupling reaction of aryl chlorides and dimethylamine. Tetrahedron Letters. 50(26). 3672–3674. 34 indexed citations
15.
Biscoe, Mark R. & Stephen L. Buchwald. (2009). Selective Monoarylation of Acetate Esters and Aryl Methyl Ketones Using Aryl Chlorides. Organic Letters. 11(8). 1773–1775. 80 indexed citations
16.
Biscoe, Mark R., Brett P. Fors, & Stephen L. Buchwald. (2008). A New Class of Easily Activated Palladium Precatalysts for Facile C−N Cross-Coupling Reactions and the Low Temperature Oxidative Addition of Aryl Chlorides. Journal of the American Chemical Society. 130(21). 6686–6687. 359 indexed citations
17.
Fors, Brett P., Donald A. Watson, Mark R. Biscoe, & Stephen L. Buchwald. (2008). A Highly Active Catalyst for Pd-Catalyzed Amination Reactions: Cross-Coupling Reactions Using Aryl Mesylates and the Highly Selective Monoarylation of Primary Amines Using Aryl Chlorides. Journal of the American Chemical Society. 130(41). 13552–13554. 451 indexed citations
18.
Biscoe, Mark R., Timothy E. Barder, & Stephen L. Buchwald. (2007). Electronic Effects on the Selectivity of Pd‐Catalyzed CN Bond‐Forming Reactions Using Biarylphosphine Ligands: The Competitive Roles of Amine Binding and Acidity. Angewandte Chemie International Edition. 46(38). 7232–7235. 92 indexed citations
19.
Biscoe, Mark R., Christopher Uyeda, & Ronald Breslow. (2004). Requirements for Selective Hydrophobic Acceleration in the Reduction of Ketones. Organic Letters. 6(23). 4331–4334. 13 indexed citations
20.
Biscoe, Mark R. & Ronald Breslow. (2003). Hydrophobically Directed Selective Reduction of Ketones. Journal of the American Chemical Society. 125(42). 12718–12719. 31 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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