| All-carbon quaternary centers in natural products and medicinal chemistry: recent advances T Ling, F Rivas Tetrahedron 72 (43), 6729-6777, 2016 | 242 | 2016 |
| Chemical synthesis of the GHIJKLMNO ring system of maitotoxin KC Nicolaou, MO Frederick, ACB Burtoloso, RM Denton, F Rivas, KP Cole, ... Journal of the American Chemical Society 130 (23), 7466-7476, 2008 | 91 | 2008 |
| Identification of Biologically Active Ganoderma lucidum Compounds and Synthesis of Improved Derivatives That Confer Anti-cancer Activities in vitro MM Martínez-Montemayor, T Ling, IJ Suárez-Arroyo, G Ortiz-Soto, ... Frontiers in pharmacology 10, 115, 2019 | 87 | 2019 |
| Synthesis of the ABCDEFG ring system of maitotoxin KC Nicolaou, RJ Aversa, J Jin, F Rivas Journal of the American Chemical Society 132 (19), 6855-6861, 2010 | 77 | 2010 |
| 3-Farnesyl-2-hydroxybenzoic acid is a new anti-Helicobacter pylori compound from Piper multiplinervium T Rüegg, AI Calderón, EF Queiroz, PN Solis, A Marston, F Rivas, ... Journal of Ethnopharmacology 103 (3), 461-467, 2006 | 64 | 2006 |
| Antimalarial activity of abietane ferruginol analogues possessing a phthalimide group MA González, J Clark, M Connelly, F Rivas Bioorganic & medicinal chemistry letters 24 (22), 5234-5237, 2014 | 63 | 2014 |
| The natural compound Jatrophone interferes with Wnt/β-catenin signaling and inhibits proliferation and EMT in human triple-negative breast cancer I Fatima, I El-Ayachi, L Taotao, MA Lillo, R Krutilina, TN Seagroves, ... PloS one 12 (12), e0189864, 2017 | 59 | 2017 |
| Advances toward the Synthesis of Functionalized γ-Lactams F Rivas, T Ling Organic Preparations and Procedures International 48 (3), 254-295, 2016 | 57 | 2016 |
| Intermolecular stereoselective iridium-catalyzed allylic alkylation: an evolutionary account SE Shockley, JC Hethcox, BM Stoltz Synlett 29 (19), 2481-2492, 2018 | 54 | 2018 |
| Antimalarial Evaluation of the Chemical Constituents of Hairy Root Culture of Bixa orellana L. B Zhai, J Clark, T Ling, M Connelly, F Medina-Bolivar, F Rivas Molecules 19 (1), 756-766, 2014 | 48 | 2014 |
| Stereoselective synthesis of the ABC ring system of norzoanthamine S Ghosh, F Rivas, D Fischer, MA González, EA Theodorakis Organic Letters 6 (6), 941-944, 2004 | 44 | 2004 |
| (+)-Dehydroabietylamine derivatives target triple-negative breast cancer T Ling, M Tran, MA Gonzalez, LN Gautam, M Connelly, RK Wood, I Fatima, ... European Journal of Medicinal Chemistry 102, 9-13, 2015 | 39 | 2015 |
| Canvass: A crowd-sourced, natural-product screening library for exploring biological space SE Kearney, G Zahoránszky-Kőhalmi, KR Brimacombe, MJ Henderson, ... ACS central science 4 (12), 1727-1741, 2018 | 38 | 2018 |
| Synthesis of (+)-and (−)-isocarvone MA González, S Ghosh, F Rivas, D Fischer, EA Theodorakis Tetrahedron letters 45 (26), 5039-5041, 2004 | 37 | 2004 |
| Evaluation of Jatropha isabelli natural products and their synthetic analogs as potential antimalarial therapeutic agents V Hadi, M Hotard, T Ling, YG Salinas, G Palacios, M Connelly, F Rivas European Journal of Medicinal Chemistry 65, 376-380, 2013 | 36* | 2013 |
| Cytostatic and cytotoxic natural products against cancer cell models T Ling, WH Lang, J Maier, M Quintana Centurion, F Rivas Molecules 24 (10), 2012, 2019 | 28 | 2019 |
| Synthesis and biological evaluation of 2′, 4′-and 3′, 4′-bridged nucleoside analogues KC Nicolaou, SP Ellery, F Rivas, K Saye, E Rogers, TJ Workinger, ... Bioorganic & medicinal chemistry 19 (18), 5648-5669, 2011 | 25 | 2011 |
| Synthetic studies toward the zoanthamine alkaloids: synthesis of the fully functionalized BC ring motif F Rivas, S Ghosh, EA Theodorakis Tetrahedron letters 46 (32), 5281-5284, 2005 | 25 | 2005 |
| Synthesis and biological studies of (+)-liquiditerpenoic acid A (abietopinoic acid) and representative analogues: SAR studies D Hamulic, M Stadler, S Hering, JM Padrón, R Bassett, F Rivas, ... Journal of natural products 82 (4), 823-831, 2019 | 24 | 2019 |
| Scalable and divergent total synthesis of (+)-colletoic acid, a selective 11β-hydroxysteroid dehydrogenase type 1 inhibitor T Ling, E Griffith, K Mitachi, F Rivas Organic letters 15 (22), 5790-5793, 2013 | 23 | 2013 |
