Stacey E. Brenner‐Moyer

497 total citations
18 papers, 405 citations indexed

About

Stacey E. Brenner‐Moyer is a scholar working on Organic Chemistry, Molecular Biology and Pharmaceutical Science. According to data from OpenAlex, Stacey E. Brenner‐Moyer has authored 18 papers receiving a total of 405 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Organic Chemistry, 6 papers in Molecular Biology and 5 papers in Pharmaceutical Science. Recurrent topics in Stacey E. Brenner‐Moyer's work include Asymmetric Synthesis and Catalysis (11 papers), Chemical Synthesis and Analysis (6 papers) and Synthetic Organic Chemistry Methods (6 papers). Stacey E. Brenner‐Moyer is often cited by papers focused on Asymmetric Synthesis and Catalysis (11 papers), Chemical Synthesis and Analysis (6 papers) and Synthetic Organic Chemistry Methods (6 papers). Stacey E. Brenner‐Moyer collaborates with scholars based in United States, Netherlands and Germany. Stacey E. Brenner‐Moyer's co-authors include Chandrakumar Appayee, Frank Jordan, Michal Szostak, Pradeep Nareddy, Joshua H. Jones, Qunsheng Guo, Paul Ha‐Yeon Cheong, Ryne C. Johnston, Ryan P. Murelli and Guang Hu and has published in prestigious journals such as ACS Catalysis, The Journal of Organic Chemistry and Chemistry - A European Journal.

In The Last Decade

Stacey E. Brenner‐Moyer

18 papers receiving 398 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Stacey E. Brenner‐Moyer United States 11 379 104 90 59 8 18 405
Xiao‐Ping Yin China 6 371 1.0× 72 0.7× 54 0.6× 58 1.0× 6 0.8× 6 385
Cui‐Tian Wang China 16 519 1.4× 62 0.6× 106 1.2× 53 0.9× 7 0.9× 23 547
Ana Pascual‐Escudero Spain 10 382 1.0× 65 0.6× 75 0.8× 42 0.7× 3 0.4× 10 399
Farid W. van der Mei United States 8 388 1.0× 109 1.0× 97 1.1× 80 1.4× 5 0.6× 9 414
Kui Liao China 11 493 1.3× 154 1.5× 160 1.8× 92 1.6× 8 1.0× 11 528
Jason J. Beiger United States 4 346 0.9× 163 1.6× 54 0.6× 51 0.9× 5 0.6× 4 367
Dhande Sudhakar Reddy Japan 9 420 1.1× 128 1.2× 259 2.9× 78 1.3× 5 0.6× 12 459
Yijing Dai United States 7 477 1.3× 105 1.0× 47 0.5× 35 0.6× 8 1.0× 8 509
Tamas Benkovics United States 10 356 0.9× 73 0.7× 28 0.3× 75 1.3× 11 1.4× 14 404
Wei‐Yu Shi China 15 552 1.5× 64 0.6× 93 1.0× 80 1.4× 15 1.9× 28 564

Countries citing papers authored by Stacey E. Brenner‐Moyer

Since Specialization
Citations

This map shows the geographic impact of Stacey E. Brenner‐Moyer'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 Stacey E. Brenner‐Moyer with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Stacey E. Brenner‐Moyer more than expected).

Fields of papers citing papers by Stacey E. Brenner‐Moyer

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Stacey E. Brenner‐Moyer. 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 Stacey E. Brenner‐Moyer. The network helps show where Stacey E. Brenner‐Moyer may publish in the future.

Co-authorship network of co-authors of Stacey E. Brenner‐Moyer

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

All Works

18 of 18 papers shown
1.
Brenner‐Moyer, Stacey E.. (2025). Building bridged bicyclic scaffolds. Nature Synthesis. 4(10). 1178–1180. 1 indexed citations
2.
Lalancette, Roger A., et al.. (2024). Organocatalytic Enantioselective [1,2]-Stevens Rearrangement of Azetidinium Salts. The Journal of Organic Chemistry. 89(12). 9063–9067. 2 indexed citations
3.
Lalancette, Roger A., et al.. (2022). DyKAT by DiCat: Stereoconvergent Dienamine-Catalyzed Claisen Rearrangements. The Journal of Organic Chemistry. 87(15). 10105–10113. 1 indexed citations
4.
Hu, Guang & Stacey E. Brenner‐Moyer. (2021). Combining Palladium and Chiral Organocatalysis for the Enantioselective Deconjugative Allylation of Enals via Dienamine Intermediates. The Journal of Organic Chemistry. 87(1). 866–873. 5 indexed citations
5.
Russo, Riccardo, et al.. (2020). Design, organocatalytic synthesis, and bioactivity evaluation of enantiopure fluorinated LpxC inhibitors. Organic & Biomolecular Chemistry. 18(30). 5867–5878. 5 indexed citations
6.
Murelli, Ryan P., et al.. (2017). Catalytic Enantioselective Intermolecular [5 + 2] Dipolar Cycloadditions of a 3-Hydroxy-4-pyrone-Derived Oxidopyrylium Ylide. Organic Letters. 19(23). 6356–6359. 19 indexed citations
7.
Hu, Guang, Kinthada Ramakumar, & Stacey E. Brenner‐Moyer. (2017). Metal- and O2-Free Oxidative C–C Bond Cleavage of Aromatic Aldehydes. The Journal of Organic Chemistry. 82(13). 6972–6977. 5 indexed citations
8.
Nareddy, Pradeep, Frank Jordan, Stacey E. Brenner‐Moyer, & Michal Szostak. (2016). Ruthenium(II)-Catalyzed Regioselective C–H Arylation of Cyclic and N,N-Dialkyl Benzamides with Boronic Acids by Weak Coordination. ACS Catalysis. 6(7). 4755–4759. 91 indexed citations
9.
Brenner‐Moyer, Stacey E., et al.. (2016). Dienamine-Catalyzed Nitrone Formation via Redox Reaction. Organic Letters. 18(9). 2146–2149. 18 indexed citations
10.
Guo, Qunsheng, et al.. (2016). Direct Diastereo- and Enantioselective Vinylogous Michael Additions of Linear Enones. Organic Letters. 18(11). 2628–2631. 29 indexed citations
11.
Brenner‐Moyer, Stacey E., et al.. (2015). An organocascade approach to α,α-chlorofluoroalcohols. Tetrahedron Letters. 56(32). 4718–4720. 11 indexed citations
12.
Jones, Joshua H., Chandrakumar Appayee, & Stacey E. Brenner‐Moyer. (2014). One‐Pot Preparation of Enantiopure Fluorinated β‐Amino Acid Precursors. European Journal of Organic Chemistry. 2014(24). 5273–5280. 12 indexed citations
13.
Johnston, Ryne C., et al.. (2012). Organocatalytic Kinetic Resolution Cascade Reactions: New Mechanistic and Stereochemical Manifold in Diphenyl Prolinol Silyl Ether Catalysis. Chemistry - A European Journal. 18(34). 10742–10752. 29 indexed citations
14.
Appayee, Chandrakumar, et al.. (2012). γ-Amino Alcohols via Organocascade Reactions Involving Dienamine Catalysis. The Journal of Organic Chemistry. 77(19). 8828–8834. 21 indexed citations
15.
Brenner‐Moyer, Stacey E., et al.. (2011). An Organocascade Kinetic Resolution. Organic Letters. 13(24). 6460–6463. 37 indexed citations
16.
Jones, Joshua H., et al.. (2011). A General Organocatalyzed Michael–Michael Cascade Reaction Generates Functionalized Cyclohexenes. The Journal of Organic Chemistry. 76(15). 6309–6319. 22 indexed citations
17.
Brenner‐Moyer, Stacey E. & Chandrakumar Appayee. (2010). Catalytic Asymmetric One-Pot Aminofluorination of Enals. Synfacts. 2010(9). 1070–1070. 1 indexed citations
18.
Appayee, Chandrakumar & Stacey E. Brenner‐Moyer. (2010). Organocatalytic Enantioselective Olefin Aminofluorination. Organic Letters. 12(15). 3356–3359. 96 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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