Jay C. Conrad

1.8k total citations
32 papers, 1.5k citations indexed

About

Jay C. Conrad is a scholar working on Organic Chemistry, Molecular Biology and Software. According to data from OpenAlex, Jay C. Conrad has authored 32 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Organic Chemistry, 14 papers in Molecular Biology and 3 papers in Software. Recurrent topics in Jay C. Conrad's work include Synthetic Organic Chemistry Methods (15 papers), Chemical Synthesis and Analysis (11 papers) and Organometallic Complex Synthesis and Catalysis (11 papers). Jay C. Conrad is often cited by papers focused on Synthetic Organic Chemistry Methods (15 papers), Chemical Synthesis and Analysis (11 papers) and Organometallic Complex Synthesis and Catalysis (11 papers). Jay C. Conrad collaborates with scholars based in United States, Canada and Norway. Jay C. Conrad's co-authors include Deryn E. Fogg, David W. C. MacMillan, J.L. Snelgrove, Brian N. Laforteza, Jongrock Kong, Glenn P. A. Yap, T. D. Beeson, Piotr Kwiatkowski, Eric R. Welin and Dino Amoroso and has published in prestigious journals such as Journal of the American Chemical Society, Angewandte Chemie International Edition and Journal of Medicinal Chemistry.

In The Last Decade

Jay C. Conrad

32 papers receiving 1.5k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jay C. Conrad United States 19 1.4k 381 249 185 74 32 1.5k
Holly J. Davis United Kingdom 11 1.4k 1.1× 233 0.6× 387 1.6× 93 0.5× 96 1.3× 14 1.6k
Brett P. Fors United States 15 2.0k 1.5× 328 0.9× 469 1.9× 104 0.6× 131 1.8× 17 2.2k
Chenguang Yu China 19 1.1k 0.8× 201 0.5× 181 0.7× 98 0.5× 224 3.0× 36 1.4k
Shashank Shekhar United States 19 1.8k 1.3× 284 0.7× 630 2.5× 104 0.6× 97 1.3× 34 1.9k
Xing‐Wen Sun China 21 1.4k 1.0× 270 0.7× 314 1.3× 58 0.3× 97 1.3× 62 1.5k
Steven F. Pedersen United States 24 1.5k 1.1× 345 0.9× 492 2.0× 69 0.4× 191 2.6× 38 1.7k
Blanka Klepetářová Czechia 23 1.3k 1.0× 452 1.2× 161 0.6× 365 2.0× 101 1.4× 111 1.7k
Zhihai Ke Hong Kong 20 985 0.7× 155 0.4× 406 1.6× 73 0.4× 220 3.0× 48 1.4k
Jillian E. Spangler United States 14 2.3k 1.7× 228 0.6× 331 1.3× 194 1.0× 44 0.6× 16 2.4k
Arianna Quintavalla Italy 23 997 0.7× 398 1.0× 142 0.6× 59 0.3× 85 1.1× 69 1.4k

Countries citing papers authored by Jay C. Conrad

Since Specialization
Citations

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

Fields of papers citing papers by Jay C. Conrad

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jay C. Conrad

This figure shows the co-authorship network connecting the top 25 collaborators of Jay C. Conrad. A scholar is included among the top collaborators of Jay C. Conrad 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 Jay C. Conrad. Jay C. Conrad 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.
Conrad, Jay C., et al.. (2024). Validating the Use of Rational Modification of Compounds to Reduce P-gp Efflux. 6(1). 34–39. 1 indexed citations
2.
Conrad, Jay C., et al.. (2024). Model of P-Glycoprotein Ligand Binding and Validation with Efflux Substrate Matched Pairs. Journal of Medicinal Chemistry. 67(7). 5854–5865. 3 indexed citations
3.
Wong, Daniel R., Jay C. Conrad, Noah R. Johnson, et al.. (2022). Trans-channel fluorescence learning improves high-content screening for Alzheimer’s disease therapeutics. Nature Machine Intelligence. 4(6). 583–595. 6 indexed citations
4.
O’Brien, Connor, Steven H. Olson, Nicholas S. Settineri, et al.. (2021). Water-Soluble Iridium Photoredox Catalyst for the Trifluoromethylation of Biomolecule Substrates in Phosphate Buffered Saline Solvent. Organic Letters. 23(10). 3823–3827. 14 indexed citations
5.
Wong, Daniel R., Jay C. Conrad, Noah R. Johnson, et al.. (2021). Trans-Channel Fluorescence Learning Improves High-Content Screening for Alzheimer's Disease Therapeutics. SSRN Electronic Journal. 1 indexed citations
6.
Aoyagi, Atsushi, Masakazu Hirouchi, Ryo Murakami, et al.. (2020). Discovery of 4-Piperazine Isoquinoline Derivatives as Potent and Brain-Permeable Tau Prion Inhibitors with CDK8 Activity. ACS Medicinal Chemistry Letters. 11(2). 127–132. 10 indexed citations
7.
O’Brien, Connor, et al.. (2018). Photoredox Cyanomethylation of Indoles: Catalyst Modification and Mechanism. The Journal of Organic Chemistry. 83(16). 8926–8935. 43 indexed citations
8.
Welin, Eric R., et al.. (2015). Enantioselective α‐Alkylation of Aldehydes by Photoredox Organocatalysis: Rapid Access to Pharmacophore Fragments from β‐Cyanoaldehydes. Angewandte Chemie International Edition. 54(33). 9668–9672. 139 indexed citations
9.
Welin, Eric R., et al.. (2015). Enantioselective α‐Alkylation of Aldehydes by Photoredox Organocatalysis: Rapid Access to Pharmacophore Fragments from β‐Cyanoaldehydes. Angewandte Chemie. 127(33). 9804–9808. 26 indexed citations
10.
Monfette, Sébastien, et al.. (2012). A Ru-isocyanate initiator for fast, living, precisely controlled ring-opening metathesis polymerization at ambient temperatures. Dalton Transactions. 41(48). 14476–14476. 5 indexed citations
11.
Devery, James J., Jay C. Conrad, David W. C. MacMillan, & Robert A. Flowers. (2010). Mechanistic Complexity in Organo–SOMO Activation. Angewandte Chemie International Edition. 49(35). 6106–6110. 66 indexed citations
12.
Gorelsky, Serge I., et al.. (2009). Geometric and Electronic Structure of aC1-Symmetric Ruthenium-Aryloxide Metathesis Catalyst: An Experimental and Computational Study. Organometallics. 28(18). 5424–5431. 18 indexed citations
13.
Conrad, Jay C., et al.. (2007). Oligomers as Intermediates in Ring-Closing Metathesis. Journal of the American Chemical Society. 129(5). 1024–1025. 92 indexed citations
14.
Delgado‐Jaime, Mario Ulises, Jay C. Conrad, Deryn E. Fogg, & Pierre Kennepohl. (2006). X-ray absorption methods for the determination of Ru–Cl bond covalency in olefin metathesis catalysts: On the normalization of chlorine K-edges in ruthenium complexes. Inorganica Chimica Acta. 359(9). 3042–3047. 17 indexed citations
15.
Conrad, Jay C., et al.. (2006). Ruthenium aryloxide catalysts: Synthesis and applications in ring-closing metathesis. Journal of Molecular Catalysis A Chemical. 254(1-2). 105–110. 14 indexed citations
16.
Conrad, Jay C., et al.. (2005). Highly Efficient Ru−Pseudohalide Catalysts for Olefin Metathesis. Journal of the American Chemical Society. 127(34). 11882–11883. 137 indexed citations
17.
Snelgrove, J.L., Jay C. Conrad, Glenn P. A. Yap, & Deryn E. Fogg. (2003). The kinetic instability of σ-bound aryloxide in coordinatively unsaturated or labile complexes of ruthenium. Inorganica Chimica Acta. 345. 268–278. 34 indexed citations
18.
Conrad, Jay C., Glenn P. A. Yap, & Deryn E. Fogg. (2003). Concise Route to Highly Reactive Ruthenium Metathesis Catalysts Containing a Labile Donor and an N-Heterocyclic Carbene (NHC) Ligand. Organometallics. 22(10). 1986–1988. 35 indexed citations
19.
Fogg, Deryn E., et al.. (2002). Ligand manipulation and design for ruthenium metathesis and tandem metathesis-hydrogenation catalysis. Journal of Molecular Catalysis A Chemical. 190(1-2). 177–184. 32 indexed citations
20.
Amoroso, Dino, J.L. Snelgrove, Jay C. Conrad, et al.. (2002). An Attractive Route to Olefin Metathesis Catalysts: Facile Synthesis of a Ruthenium Alkylidene Complex Containing Labile Phosphane Donors. Advanced Synthesis & Catalysis. 344(6-7). 757–757. 48 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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