Diana C. Reeves

863 total citations
19 papers, 613 citations indexed

About

Diana C. Reeves is a scholar working on Organic Chemistry, Inorganic Chemistry and Molecular Biology. According to data from OpenAlex, Diana C. Reeves has authored 19 papers receiving a total of 613 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Organic Chemistry, 11 papers in Inorganic Chemistry and 8 papers in Molecular Biology. Recurrent topics in Diana C. Reeves's work include Asymmetric Hydrogenation and Catalysis (11 papers), Chemical Synthesis and Analysis (8 papers) and Surface Chemistry and Catalysis (4 papers). Diana C. Reeves is often cited by papers focused on Asymmetric Hydrogenation and Catalysis (11 papers), Chemical Synthesis and Analysis (8 papers) and Surface Chemistry and Catalysis (4 papers). Diana C. Reeves collaborates with scholars based in United States, Germany and Japan. Diana C. Reeves's co-authors include Chris H. Senanayake, Nizar Haddad, Heewon Lee, Sonia Rodrı́guez, Dhileepkumar Krishnamurthy, Yibo Xu, Bruce Z. Lu, Jonathan T. Reeves, Zhulin Tan and Zhengxu S. Han and has published in prestigious journals such as Angewandte Chemie International Edition, Organic Letters and Tetrahedron Letters.

In The Last Decade

Diana C. Reeves

19 papers receiving 599 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Diana C. Reeves United States 13 553 272 170 42 24 19 613
Zongxuan Shen China 12 340 0.6× 176 0.6× 94 0.6× 56 1.3× 17 0.7× 32 404
Nolwenn J. A. Martin Germany 5 712 1.3× 379 1.4× 204 1.2× 76 1.8× 22 0.9× 5 778
Mireia Pastó Spain 13 373 0.7× 131 0.5× 183 1.1× 38 0.9× 11 0.5× 18 433
Hirofumi Matsunaga Japan 14 455 0.8× 143 0.5× 97 0.6× 28 0.7× 21 0.9× 41 515
Fuk Loi Lam Hong Kong 10 499 0.9× 317 1.2× 102 0.6× 79 1.9× 15 0.6× 11 566
Amélie Roy United States 9 474 0.9× 196 0.7× 98 0.6× 28 0.7× 11 0.5× 15 529
Philippe Dellis France 8 577 1.0× 523 1.9× 151 0.9× 142 3.4× 47 2.0× 11 709
Martin Kesselgruber Germany 9 459 0.8× 273 1.0× 102 0.6× 42 1.0× 11 0.5× 15 496
Sébastien Duprat de Paule France 8 566 1.0× 504 1.9× 138 0.8× 139 3.3× 50 2.1× 9 702
Yasunori Tsuchiya Japan 7 498 0.9× 335 1.2× 95 0.6× 61 1.5× 31 1.3× 10 558

Countries citing papers authored by Diana C. Reeves

Since Specialization
Citations

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

Fields of papers citing papers by Diana C. Reeves

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Diana C. Reeves. 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 Diana C. Reeves. The network helps show where Diana C. Reeves may publish in the future.

Co-authorship network of co-authors of Diana C. Reeves

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

All Works

19 of 19 papers shown
1.
Eriksson, Magnus, Xingzhong Zeng, Jinghua Xu, et al.. (2018). The Guareschi–Thorpe Cyclization Revisited – An Efficient Synthesis of Substituted 2,6-Dihydroxypyridines and 2,6-Dichloropyridines. Synlett. 29(11). 1455–1460. 3 indexed citations
2.
Reeves, Jonathan T., Zhulin Tan, Diana C. Reeves, et al.. (2014). Development of an Enantioselective Hydrogenation Route to (S)-1-(2-(Methylsulfonyl)pyridin-4-yl)propan-1-amine. Organic Process Research & Development. 18(7). 904–911. 18 indexed citations
3.
Frutos, Rogelio P., et al.. (2014). A General and Practical Synthesis of N‐Aryl‐3‐[4‐(imidazol‐4‐yl)‐1,2,3‐triazol‐1‐yl]benzamide Anti‐Inflammatory Cytokine Inhibitors. Asian Journal of Organic Chemistry. 3(7). 769–772. 4 indexed citations
4.
Busacca, Carl A., Bo Qu, Keith R. Fandrick, et al.. (2013). Tuning the Peri Effect for Enantioselectivity: Asymmetric Hydrogenation of Unfunctionalized Olefins with the BIPI Ligands. Advanced Synthesis & Catalysis. 355(8). 1455–1463. 30 indexed citations
5.
Reeves, Jonathan T., Zhulin Tan, Maurice A. Marsini, et al.. (2013). A Practical Procedure for Reduction of Primary, Secondary and Tertiary Amides to Amines. Advanced Synthesis & Catalysis. 355(1). 47–52. 91 indexed citations
6.
Zhang, Yongda, Ning Li, Bo Qu, et al.. (2013). Asymmetric Methallylation of Ketones Catalyzed by a Highly Active Organocatalyst 3,3′-F2-BINOL. Organic Letters. 15(7). 1710–1713. 48 indexed citations
7.
Busacca, Carl A., Jon C. Lorenz, Anjan K. Saha, et al.. (2012). Development of the BIPI ligands for asymmetric hydrogenation. Catalysis Science & Technology. 2(10). 2083–2083. 12 indexed citations
8.
Reeves, Jonathan T., Zhulin Tan, Zhengxu S. Han, et al.. (2012). Direct Titanium‐Mediated Conversion of Ketones into Enamides with Ammonia and Acetic Anhydride. Angewandte Chemie International Edition. 51(6). 1400–1404. 52 indexed citations
9.
Qu, Bo, Nizar Haddad, Sonia Rodrı́guez, et al.. (2012). Chelation controlled reductive amination of cyclic ketones to trans-4-methoxycyclohexylamines: 9-BBN reduction mediated with FeCl3. Tetrahedron Letters. 53(15). 1982–1986. 3 indexed citations
10.
Reeves, Jonathan T., Zhulin Tan, Zhengxu S. Han, et al.. (2012). Direct Titanium‐Mediated Conversion of Ketones into Enamides with Ammonia and Acetic Anhydride. Angewandte Chemie. 124(6). 1429–1433. 12 indexed citations
11.
Frutos, Rogelio P., Jason A. Mulder, Yibo Xu, et al.. (2011). A new and practical boronic acid catalyzed intramolecular cyclodehydration of ureas for the synthesis of LFA-1 antagonists. Tetrahedron Letters. 52(19). 2465–2467. 6 indexed citations
12.
Haddad, Nizar, Bo Qu, Sonia Rodrı́guez, et al.. (2011). Catalytic asymmetric hydrogenation of heterocyclic ketone-derived hydrazones, pronounced solvent effect on the inversion of configuration. Tetrahedron Letters. 52(29). 3718–3722. 24 indexed citations
13.
Rodrı́guez, Sonia, Bo Qu, Nizar Haddad, et al.. (2011). Oxaphosphole‐Based Monophosphorus Ligands for Palladium‐Catalyzed Amination Reactions. Advanced Synthesis & Catalysis. 353(4). 533–537. 51 indexed citations
14.
Reeves, Diana C., Sonia Rodrı́guez, Heewon Lee, et al.. (2011). Palladium Catalyzed Alkoxy- and Aminocarbonylation of Vinyl Tosylates. Organic Letters. 13(9). 2495–2497. 34 indexed citations
15.
Reeves, Diana C., Sonia Rodrı́guez, Heewon Lee, et al.. (2009). Palladium-catalyzed coupling of vinyl tosylates with arylsulfinate salts. Tetrahedron Letters. 50(24). 2870–2873. 74 indexed citations
16.
Wang, Xiao‐jun, Kanwar Sidhu, Li Zhang, et al.. (2009). Bromo-Directed N-2 Alkylation of NH-1,2,3-Triazoles: Efficient Synthesis of Poly-Substituted 1,2,3-Triazoles. Organic Letters. 11(23). 5490–5493. 55 indexed citations
17.
Busacca, Carl A., Scot Campbell, Nina C. Gonnella, et al.. (2009). Ambient Temperature Hydrophosphination of Internal, Unactivated Alkynes and Allenyl Phosphineoxides with Phosphine Borane Complexes. Organic Letters. 11(24). 5594–5597. 37 indexed citations
18.
Busacca, Carl A., Jon C. Lorenz, Nelu Grinberg, et al.. (2007). Asymmetric Hydrogenation of Unsaturated Ureas with the BIPI Ligands. Organic Letters. 10(2). 341–344. 39 indexed citations
19.
Frutos, Rogelio P., Isabelle Gallou, Diana C. Reeves, et al.. (2005). Expedient synthesis of substituted imidazoles from nitriles. Tetrahedron Letters. 46(48). 8369–8372. 20 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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