Jeremy A. May

2.2k total citations
68 papers, 1.9k citations indexed

About

Jeremy A. May is a scholar working on Organic Chemistry, Molecular Biology and Pharmacology. According to data from OpenAlex, Jeremy A. May has authored 68 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 43 papers in Organic Chemistry, 11 papers in Molecular Biology and 9 papers in Pharmacology. Recurrent topics in Jeremy A. May's work include Cyclopropane Reaction Mechanisms (19 papers), Catalytic C–H Functionalization Methods (17 papers) and Asymmetric Synthesis and Catalysis (15 papers). Jeremy A. May is often cited by papers focused on Cyclopropane Reaction Mechanisms (19 papers), Catalytic C–H Functionalization Methods (17 papers) and Asymmetric Synthesis and Catalysis (15 papers). Jeremy A. May collaborates with scholars based in United States, South Korea and Taiwan. Jeremy A. May's co-authors include Brian M. Stoltz, Santa Jansone‐Popova, Truong N. Nguyen, Thien S. Nguyen, Ryan K. Zeidan, Amanda C. Jones, Richmond Sarpong, Ryan R. Julian, Po‐An Chen and J. L. Beauchamp and has published in prestigious journals such as Journal of the American Chemical Society, Angewandte Chemie International Edition and Nature Communications.

In The Last Decade

Jeremy A. May

66 papers receiving 1.9k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jeremy A. May United States 26 1.5k 256 217 146 122 68 1.9k
Kentaro Okano Japan 24 1.6k 1.0× 283 1.1× 180 0.8× 195 1.3× 98 0.8× 120 1.9k
Yungui Peng China 26 1.9k 1.2× 317 1.2× 511 2.4× 59 0.4× 66 0.5× 85 2.2k
Yoshiro Hirai Japan 23 1.2k 0.8× 279 1.1× 139 0.6× 82 0.6× 117 1.0× 99 1.4k
Santosh J. Gharpure India 27 1.7k 1.1× 257 1.0× 137 0.6× 29 0.2× 93 0.8× 116 2.0k
Brian L. Pagenkopf United States 33 3.0k 1.9× 373 1.5× 353 1.6× 78 0.5× 68 0.6× 78 3.4k
Saumen Hajra India 27 1.6k 1.0× 340 1.3× 293 1.4× 47 0.3× 56 0.5× 86 1.9k
Fu‐She Han China 29 2.9k 1.9× 279 1.1× 691 3.2× 125 0.9× 61 0.5× 82 3.1k
Andrew G. H. Wee Canada 22 872 0.6× 213 0.8× 174 0.8× 67 0.5× 64 0.5× 56 1.5k
Ryo Takita Japan 25 1.9k 1.2× 288 1.1× 496 2.3× 76 0.5× 86 0.7× 73 2.3k
Brandon R. Rosen United States 10 2.0k 1.3× 166 0.6× 243 1.1× 55 0.4× 42 0.3× 20 2.3k

Countries citing papers authored by Jeremy A. May

Since Specialization
Citations

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

Fields of papers citing papers by Jeremy A. May

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jeremy A. May. 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 Jeremy A. May. The network helps show where Jeremy A. May may publish in the future.

Co-authorship network of co-authors of Jeremy A. May

This figure shows the co-authorship network connecting the top 25 collaborators of Jeremy A. May. A scholar is included among the top collaborators of Jeremy A. May 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 Jeremy A. May. Jeremy A. May 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.
May, Jeremy A., et al.. (2024). Can Twisted Double Bonds Facilitate Stepwise [2 + 2] Cycloadditions?. Organic Letters. 26(18). 3778–3783. 5 indexed citations
2.
May, Jeremy A., et al.. (2024). Photoactivation of Hydrazones for the Synthesis of Diarylalkanes and Trialkylmethylboronates: The Key Role Played by Soluble Base. Organic Letters. 26(16). 3397–3400. 5 indexed citations
3.
May, Jeremy A., et al.. (2024). Regio- and enantioselective synthesis of acyclic quaternary carbons via organocatalytic addition of organoborates to (Z)-Enediketones. Nature Communications. 15(1). 504–504. 5 indexed citations
4.
5.
May, Jeremy A., et al.. (2021). Reaction rate differences between organotrifluoroborates and boronic acids in BINOL-catalyzed conjugate addition to enones. Tetrahedron Letters. 83. 153412–153412. 7 indexed citations
6.
May, Jeremy A., Haoyu Zhu, Md. Humayun Kabir, et al.. (2021). Highly Stable, Low-Cost Metal-Free Oxygen Reduction Reaction Electrocatalyst Based on Nitrogen-Doped Pseudo-Graphite. Energy & Fuels. 35(12). 10146–10155. 6 indexed citations
7.
Nguyen, Nam T., et al.. (2021). Engineering Escherichia coli for anaerobic alkane activation: Biosynthesis of (1‐methylalkyl)succinates. Biotechnology and Bioengineering. 119(1). 315–320. 5 indexed citations
8.
May, Jeremy A., et al.. (2020). Formation of β-Oxo-N-vinylimidates via Intermolecular Ester Incorporation in Huisgen Cyclization/Carbene Cascade Reactions. Organic Letters. 22(24). 9579–9584. 7 indexed citations
9.
Nguyen, Truong N., et al.. (2018). Chiral Diol-Based Organocatalysts in Enantioselective Reactions. Molecules. 23(9). 2317–2317. 40 indexed citations
10.
11.
12.
Nguyen, Truong N. & Jeremy A. May. (2017). Enantioselective organocatalytic conjugate addition of organoboron nucleophiles. Tetrahedron Letters. 58(16). 1535–1544. 37 indexed citations
13.
Chen, Po‐An & Jeremy A. May. (2016). Hydrazone‐Initiated Reaction Cascades. Asian Journal of Organic Chemistry. 5(11). 1296–1303. 14 indexed citations
14.
Nguyen, Thien S., et al.. (2015). Organocatalyzed Asymmetric Conjugate Addition of Heteroaryl and Aryl Trifluoroborates: a Synthetic Strategy for Discoipyrrole D. Angewandte Chemie International Edition. 54(34). 9931–9935. 70 indexed citations
15.
Smuts, Jonathan, et al.. (2013). Enantioseparation of flinderoles and borreverines by HPLC on Chirobiotic V and V2 stationary phases and by CE using cyclodextrin selectors. Analytical and Bioanalytical Chemistry. 405(28). 9169–9177. 7 indexed citations
16.
May, Jeremy A., et al.. (2012). Biomimetic Synthesis of the Antimalarial Flindersial Alkaloids. Journal of the American Chemical Society. 134(16). 6936–6939. 69 indexed citations
17.
Jansone‐Popova, Santa & Jeremy A. May. (2012). Synthesis of Bridged Polycyclic Ring Systems via Carbene Cascades Terminating in C–H Bond Insertion. Journal of the American Chemical Society. 134(43). 17877–17880. 73 indexed citations
18.
May, Jeremy A., Ryan K. Zeidan, & Brian M. Stoltz. (2003). Biomimetic Approach to Communesin B (a.k.a. Nomofungin).. ChemInform. 34(18). 87 indexed citations
19.
Julian, Ryan R., Jeremy A. May, Brian M. Stoltz, & J. L. Beauchamp. (2003). Gas-Phase Synthesis of Charged Copper and Silver Fischer Carbenes from Diazomalonates:  Mechanistic and Conformational Considerations in Metal-Mediated Wolff Rearrangements. Journal of the American Chemical Society. 125(15). 4478–4486. 56 indexed citations
20.
Julian, Ryan R., Jeremy A. May, Brian M. Stoltz, & J. L. Beauchamp. (2003). Molecular Mousetraps: Gas‐Phase Studies of the Covalent Coupling of Noncovalent Complexes Initiated by Reactive Carbenes Formed by Controlled Activation of Diazo Precursors. Angewandte Chemie International Edition. 42(9). 1012–1015. 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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