Mitchell P. Croatt

1.3k total citations
39 papers, 963 citations indexed

About

Mitchell P. Croatt is a scholar working on Organic Chemistry, Molecular Biology and Pharmacology. According to data from OpenAlex, Mitchell P. Croatt has authored 39 papers receiving a total of 963 indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Organic Chemistry, 13 papers in Molecular Biology and 6 papers in Pharmacology. Recurrent topics in Mitchell P. Croatt's work include Catalytic C–H Functionalization Methods (16 papers), Catalytic Alkyne Reactions (9 papers) and Oxidative Organic Chemistry Reactions (6 papers). Mitchell P. Croatt is often cited by papers focused on Catalytic C–H Functionalization Methods (16 papers), Catalytic Alkyne Reactions (9 papers) and Oxidative Organic Chemistry Reactions (6 papers). Mitchell P. Croatt collaborates with scholars based in United States, Mexico and Jordan. Mitchell P. Croatt's co-authors include Paul A. Wender, B. Witulski, Nicole M. Deschamps, I. F. Dempsey Hyatt, Nicholas H. Oberlies, Erick M. Carreira, Thomas J. Dietz, Cedric J. Pearce, Patricia H. Reggio and Dow P. Hurst and has published in prestigious journals such as Journal of the American Chemical Society, Angewandte Chemie International Edition and Biochemistry.

In The Last Decade

Mitchell P. Croatt

38 papers receiving 946 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Mitchell P. Croatt United States 17 683 275 161 111 57 39 963
Lilian Alcaraz United Kingdom 23 1.0k 1.5× 471 1.7× 214 1.3× 116 1.0× 45 0.8× 44 1.4k
Takahiko Taniguchi Japan 22 1.1k 1.6× 649 2.4× 181 1.1× 115 1.0× 44 0.8× 78 1.5k
S. L. Manju India 14 889 1.3× 242 0.9× 235 1.5× 84 0.8× 15 0.3× 35 1.2k
Pilar López‐Alvarado Spain 18 732 1.1× 247 0.9× 105 0.7× 74 0.7× 10 0.2× 53 976
Susumu Mitsumori Japan 11 600 0.9× 255 0.9× 128 0.8× 140 1.3× 13 0.2× 15 785
Suckchang Hong South Korea 21 692 1.0× 370 1.3× 130 0.8× 221 2.0× 16 0.3× 61 1.1k
Raghuram Rao Akkinepally India 15 480 0.7× 238 0.9× 117 0.7× 28 0.3× 15 0.3× 49 800
Mohd. Javed Naim India 18 844 1.2× 361 1.3× 156 1.0× 35 0.3× 13 0.2× 40 1.2k
Erika M. Milczek United States 11 536 0.8× 242 0.9× 85 0.5× 169 1.5× 7 0.1× 12 812
Ronald C. Bernotas United States 19 951 1.4× 549 2.0× 130 0.8× 66 0.6× 9 0.2× 43 1.2k

Countries citing papers authored by Mitchell P. Croatt

Since Specialization
Citations

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

Fields of papers citing papers by Mitchell P. Croatt

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mitchell P. Croatt

This figure shows the co-authorship network connecting the top 25 collaborators of Mitchell P. Croatt. A scholar is included among the top collaborators of Mitchell P. Croatt 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 Mitchell P. Croatt. Mitchell P. Croatt 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
2.
Croatt, Mitchell P., et al.. (2022). Prostacyclin (PGI2) scaffolds in medicinal chemistry: current and emerging drugs. Medicinal Chemistry Research. 31(8). 1241–1251. 1 indexed citations
3.
Raja, Huzefa A., et al.. (2021). Media and strain studies for the scaled production of cis-enone resorcylic acid lactones as feedstocks for semisynthesis. The Journal of Antibiotics. 74(8). 496–507. 8 indexed citations
4.
Croatt, Mitchell P., et al.. (2018). Synthetic approaches to isocarbacyclin and analogues as potential neuroprotective agents against ischemic stroke. Bioorganic & Medicinal Chemistry. 27(2). 338–342. 1 indexed citations
5.
Cook, Christopher David, Linda Console‐Bram, Dow P. Hurst, et al.. (2017). Design, synthesis and biological evaluation of GPR55 agonists. Bioorganic & Medicinal Chemistry. 25(16). 4355–4367. 14 indexed citations
6.
Hyatt, I. F. Dempsey, et al.. (2017). Hypervalent Iodonium Alkynyl Triflate Generated Phenylcyanocarbene and Its Reactivity with Aromatic Systems. The Journal of Organic Chemistry. 82(22). 11772–11780. 19 indexed citations
7.
Paguigan, Noemi D., Huzefa A. Raja, Joanna E. Burdette, et al.. (2017). Chemoselective fluorination and chemoinformatic analysis of griseofulvin: Natural vs fluorinated fungal metabolites. Bioorganic & Medicinal Chemistry. 25(20). 5238–5246. 12 indexed citations
8.
Hyatt, I. F. Dempsey, et al.. (2017). Decarboxylative and dehydrative coupling of dienoic acids and pentadienyl alcohols to form 1,3,6,8-tetraenes. Beilstein Journal of Organic Chemistry. 13. 384–392. 10 indexed citations
9.
Console‐Bram, Linda, Thomas F. Gamage, Haleli Sharir, et al.. (2016). Design, synthesis, and analysis of antagonists of GPR55: Piperidine-substituted 1,3,4-oxadiazol-2-ones. Bioorganic & Medicinal Chemistry Letters. 26(7). 1827–1830. 5 indexed citations
10.
Zhao, Pingwei, et al.. (2016). Structure-activity relationships of benzothiazole GPR35 antagonists. Bioorganic & Medicinal Chemistry Letters. 27(3). 612–615. 6 indexed citations
11.
Sy‐Cordero, Arlene A., Mario Figueroa, Huzefa A. Raja, et al.. (2015). Spiroscytalin, a new tetramic acid and other metabolites of mixed biogenesis from Scytalidium cuboideum. Tetrahedron. 71(47). 8899–8904. 15 indexed citations
12.
El‐Elimat, Tamam, Dow P. Hurst, Patricia H. Reggio, et al.. (2015). Isolation, semisynthesis, covalent docking and transforming growth factor beta-activated kinase 1 (TAK1)-inhibitory activities of (5Z)-7-oxozeaenol analogues. Bioorganic & Medicinal Chemistry. 23(21). 6993–6999. 20 indexed citations
13.
Hyatt, I. F. Dempsey, et al.. (2013). Synthesis of Hypervalent Iodonium Alkynyl Triflates for the Application of Generating Cyanocarbenes. Journal of Visualized Experiments. 1 indexed citations
14.
Graf, Tyler N., Arlene A. Sy‐Cordero, Brandon T. Gufford, et al.. (2013). Semisynthesis, cytotoxicity, antiviral activity, and drug interaction liability of 7-O-methylated analogues of flavonolignans from milk thistle. Bioorganic & Medicinal Chemistry. 21(13). 3919–3926. 23 indexed citations
15.
Kotsikorou, Evangelia, Haleli Sharir, Derek M. Shore, et al.. (2013). Identification of the GPR55 Antagonist Binding Site Using a Novel Set of High-Potency GPR55 Selective Ligands. Biochemistry. 52(52). 9456–9469. 69 indexed citations
16.
Oberlies, Nicholas H., et al.. (2013). Mechanistic Study of the Biomimetic Synthesis of Flavonolignan Diastereoisomers in Milk Thistle. The Journal of Organic Chemistry. 78(15). 7594–7600. 63 indexed citations
17.
Hyatt, I. F. Dempsey & Mitchell P. Croatt. (2012). Reactions of Hypervalent Iodonium Alkynyl Triflates with Azides: Generation of Cyanocarbenes. Angewandte Chemie International Edition. 51(30). 7511–7514. 36 indexed citations
18.
Dietz, Thomas J., et al.. (2011). Selective Formation of 1,5-Substituted Sulfonyl Triazoles Using Acetylides and Sulfonyl Azides. Organic Letters. 13(12). 2984–2987. 68 indexed citations
19.
Wender, Paul A., et al.. (2009). Rhodium(I)-Catalyzed [2+2], [2+2+2], and [2+2+2+2] Cycloadditions of Dienes or Alkynes with a Bis-ene. Organometallics. 28(20). 5841–5844. 16 indexed citations
20.
Wender, Paul A., Mitchell P. Croatt, & Nicole M. Deschamps. (2006). Metal‐Catalyzed [2+2+1] Cycloadditions of 1,3‐Dienes, Allenes, and CO. Angewandte Chemie International Edition. 45(15). 2459–2462. 52 indexed citations

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