Flavio Cardoso
Affiliations: | 2009-2014 | Department of Chemistry | University of Florida, Gainesville, Gainesville, FL, United States |
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| Lucas T, Dietz JP, Cardoso FSP, et al. (2023) Short and Efficient Synthesis of the Antituberculosis Agent Pretomanid from ()-Glycidol. Organic Process Research & Development. 27: 1641-1651 |
| Cardoso FSP, Kadam AL, Nelson RC, et al. (2023) Practical and Scalable Two-Step Process for 6-(2-Fluoro-4-nitrophenyl)-2-oxa-6-azaspiro[3.3]heptane: A Key Intermediate of the Potent Antibiotic Drug Candidate TBI-223. Organic Process Research & Development. 27: 1390-1399 |
| Vasudevan N, Ahlqvist GP, McGeough CP, et al. (2020) A concise route to MK-4482 (EIDD-2801) from cytidine. Chemical Communications (Cambridge, England) |
| Paymode DJ, Cardoso FSP, Agrawal T, et al. (2020) Expanding Access to Remdesivir via an Improved Pyrrolotriazine Synthesis: Supply Centered Synthesis. Organic Letters |
| Cardoso FSP, Mickle GE, Da Silva MA, et al. (2016) Application of in Situ FTIR for the Preparation of 17-α-Estradiol via Mitsunobu Reaction Organic Process Research and Development. 20: 306-311 |
| Pappoppula M, Cardoso FS, Garrett BO, et al. (2015) Enantioselective Copper-Catalyzed Quinoline Alkynylation. Angewandte Chemie (International Ed. in English) |
| Cardoso FS, Abboud KA, Aponick A. (2013) Design, preparation, and implementation of an imidazole-based chiral biaryl P,N-ligand for asymmetric catalysis. Journal of the American Chemical Society. 135: 14548-51 |
| Ketcham JM, Cardoso FSP, Biannic B, et al. (2013) Nitrogen nucleophiles in au-catalyzed dehydrative cyclization reactions Israel Journal of Chemistry. 53: 923-931 |
| Moro AV, Cardoso FS, Correia CR. (2009) Highly regio- and stereoselective Heck reaction of allylic esters with arenediazonium salts: application to the synthesis of kavalactones. Organic Letters. 11: 3642-5 |
| Moro AV, Cardoso FSP, Correia CRD. (2008) Heck arylation of styrenes with arenediazonium salts: short, efficient, and stereoselective synthesis of resveratrol, DMU-212, and analogues Tetrahedron Letters. 49: 5668-5671 |