Mary P. Watson

4.0k total citations
50 papers, 3.3k citations indexed

About

Mary P. Watson is a scholar working on Organic Chemistry, Inorganic Chemistry and Molecular Biology. According to data from OpenAlex, Mary P. Watson has authored 50 papers receiving a total of 3.3k indexed citations (citations by other indexed papers that have themselves been cited), including 46 papers in Organic Chemistry, 10 papers in Inorganic Chemistry and 6 papers in Molecular Biology. Recurrent topics in Mary P. Watson's work include Catalytic C–H Functionalization Methods (37 papers), Catalytic Cross-Coupling Reactions (26 papers) and Asymmetric Synthesis and Catalysis (17 papers). Mary P. Watson is often cited by papers focused on Catalytic C–H Functionalization Methods (37 papers), Catalytic Cross-Coupling Reactions (26 papers) and Asymmetric Synthesis and Catalysis (17 papers). Mary P. Watson collaborates with scholars based in United States and United Kingdom. Mary P. Watson's co-authors include Corey H. Basch, Harathi D. Srinivas, Qi Zhou, Srimoyee Dasgupta, Jennie Liao, Prantik Maity, Eric N. Jacobsen, Jianyu Xu, Danielle M. Shacklady‐McAtee and Glenn P. A. Yap and has published in prestigious journals such as Journal of the American Chemical Society, Angewandte Chemie International Edition and Chemical Communications.

In The Last Decade

Mary P. Watson

47 papers receiving 3.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Mary P. Watson United States 30 3.2k 731 271 201 71 50 3.3k
Takashi Nishikata Japan 34 3.4k 1.1× 781 1.1× 382 1.4× 246 1.2× 125 1.8× 102 3.7k
Alexander M. Haydl Germany 18 1.5k 0.5× 465 0.6× 172 0.6× 61 0.3× 61 0.9× 21 1.7k
Xing‐Zhong Shu China 43 4.5k 1.4× 856 1.2× 205 0.8× 244 1.2× 93 1.3× 99 4.8k
Yanzhao Wang United States 19 2.1k 0.7× 434 0.6× 143 0.5× 101 0.5× 43 0.6× 30 2.2k
Wanxiang Zhao China 25 2.1k 0.7× 419 0.6× 265 1.0× 89 0.4× 62 0.9× 83 2.4k
Michael C. Haibach United States 15 1.3k 0.4× 522 0.7× 116 0.4× 58 0.3× 97 1.4× 24 1.5k

Countries citing papers authored by Mary P. Watson

Since Specialization
Citations

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

Fields of papers citing papers by Mary P. Watson

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Mary P. Watson. 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 Mary P. Watson. The network helps show where Mary P. Watson may publish in the future.

Co-authorship network of co-authors of Mary P. Watson

This figure shows the co-authorship network connecting the top 25 collaborators of Mary P. Watson. A scholar is included among the top collaborators of Mary P. Watson 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 Mary P. Watson. Mary P. Watson 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.
Fu, Jiantao, Rajdip Chowdhury, Yu‐hong Lam, et al.. (2023). Nickel-Catalyzed Electroreductive Coupling of Alkylpyridinium Salts and Aryl Halides. ACS Catalysis. 13(14). 9336–9345. 21 indexed citations
2.
Dimitrakellis, Panagiotis, Michael R. Talley, Robert M. O’Dea, et al.. (2022). Oxidative Functionalization of Long-Chain Liquid Alkanes by Pulsed Plasma Discharges at Atmospheric Pressure. ACS Sustainable Chemistry & Engineering. 10(48). 15749–15759. 15 indexed citations
3.
Hinton, Zachary R., Michael R. Talley, Pavel A. Kots, et al.. (2022). Innovations Toward the Valorization of Plastics Waste. Annual Review of Materials Research. 52(1). 249–280. 42 indexed citations
4.
Xu, Jianyu, et al.. (2021). Nickel-Catalyzed, Stereospecific C–C and C–B Cross-Couplings via C–N and C–O Bond Activation. ACS Catalysis. 11(3). 1604–1612. 65 indexed citations
5.
Plunkett, Shane, et al.. (2019). Engaging Alkenes and Alkynes in Deaminative Alkyl–Alkyl and Alkyl–Vinyl Cross-Couplings of Alkylpyridinium Salts. Organic Letters. 21(23). 9738–9741. 41 indexed citations
6.
Plunkett, Shane, et al.. (2019). Harnessing Alkylpyridinium Salts as Electrophiles in Deaminative Alkyl–Alkyl Cross-Couplings. Journal of the American Chemical Society. 141(6). 2257–2262. 154 indexed citations
7.
Watson, Mary P., et al.. (2018). Asymmetric synthesisviastereospecific C–N and C–O bond activation of alkyl amine and alcohol derivatives. Chemical Communications. 54(87). 12286–12301. 60 indexed citations
8.
Watson, Mary P., et al.. (2018). Vinylation of Benzylic Amines via C–N Bond Functionalization of Benzylic Pyridinium Salts. Synthesis. 50(16). 3231–3237. 53 indexed citations
9.
Basch, Corey H., et al.. (2017). Harnessing Alkyl Amines as Electrophiles for Nickel-Catalyzed Cross Couplings via C–N Bond Activation. Journal of the American Chemical Society. 139(15). 5313–5316. 288 indexed citations
10.
Cobb, K. M., et al.. (2017). Stereospecific, Nickel-Catalyzed Suzuki–Miyaura Cross-Coupling of Allylic Pivalates To Deliver Quaternary Stereocenters. Organic Letters. 19(16). 4355–4358. 28 indexed citations
11.
Liu, Jixin, Srimoyee Dasgupta, & Mary P. Watson. (2015). Enantioselective additions of copper acetylides to cyclic iminium and oxocarbenium ions. Beilstein Journal of Organic Chemistry. 11. 2696–2706. 28 indexed citations
12.
Watson, Mary P., et al.. (2015). Stereoselective Synthesis of Trisubstituted Vinyl Bromides by Addition of Alkynes to Oxocarbenium Ions. Synlett. 26(19). 2702–2706. 3 indexed citations
13.
Dasgupta, Srimoyee, et al.. (2015). Enantioselective Copper(I)‐Catalyzed Alkynylation of Oxocarbenium Ions to Set Diaryl Tetrasubstituted Stereocenters. Angewandte Chemie International Edition. 54(47). 14154–14158. 70 indexed citations
14.
Shacklady‐McAtee, Danielle M., et al.. (2014). A general, simple catalyst for enantiospecific cross couplings of benzylic ammonium triflates and boronic acids: no phosphine ligand required. Tetrahedron. 70(27-28). 4257–4263. 60 indexed citations
15.
Maity, Prantik, Danielle M. Shacklady‐McAtee, Glenn P. A. Yap, Eric R. Sirianni, & Mary P. Watson. (2012). Nickel-Catalyzed Cross Couplings of Benzylic Ammonium Salts and Boronic Acids: Stereospecific Formation of Diarylethanes via C–N Bond Activation. Journal of the American Chemical Society. 135(1). 280–285. 256 indexed citations
16.
Zhou, Qi, et al.. (2012). Nickel(0)-Catalyzed Heck Cross-Coupling via Activation of Aryl C–OPiv Bonds. Organic Letters. 14(5). 1202–1205. 132 indexed citations
17.
Watson, Mary P. & Prantik Maity. (2012). Controlling Enantioselectivity in Additions to Cyclic Oxocarbenium Ions via Transition-Metal Catalysis. Synlett. 23(12). 1705–1708. 13 indexed citations
18.
Watson, Mary P., et al.. (2008). Nickel-Catalyzed C-CN Bond Activation and AsymmetricArylcyanation. Synfacts. 2008(12). 1287–1287.
19.
Kirsch, Stefan F., Larry E. Overman, & Mary P. Watson. (2005). Monomeric Cobalt Oxazoline Palladacycles (COP). Useful Catalysts for Catalytic Asymmetric Rearrangement of Allylic Trichloroacetimidates.. ChemInform. 36(12). 1 indexed citations
20.
Kirsch, Stefan F., Larry E. Overman, & Mary P. Watson. (2004). Monomeric Cobalt Oxazoline Palladacycles (COP). Useful Catalysts for Catalytic Asymmetric Rearrangement of Allylic Trichloroacetimidates. The Journal of Organic Chemistry. 69(23). 8101–8104. 94 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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