Troy Ryba
Affiliations: | Scripps Research Institute Florida |
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"Troy Ryba"Mean distance: 7.84 | S | N | B | C | P |
Parents
Sign in to add mentor| Thomas Robert Hoye | grad student | 2005 | UMN | |
| (Efforts towards a total synthesis of (+)-peloruside A.) | ||||
| William R. Roush | post-doc | Scripps Research Institute Florida | ||
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Publications
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| Pandya BA, Dandapani S, Duvall JR, et al. (2011) Practical asymmetric synthesis of β-hydroxy γ-amino acids via complimentary aldol reactions. Tetrahedron. 67: 6131-6137 |
| Marcaurelle LA, Comer E, Dandapani S, et al. (2010) An aldol-based build/couple/pair strategy for the synthesis of medium- and large-sized rings: discovery of macrocyclic histone deacetylase inhibitors. Journal of the American Chemical Society. 132: 16962-76 |
| Hoye TR, Jeon J, Kopel LC, et al. (2010) Total synthesis of peloruside A through kinetic lactonization and relay ring-closing metathesis cyclization reactions. Angewandte Chemie (International Ed. in English). 49: 6151-5 |
| Hoye T, Jeon J, Kopel L, et al. (2010) Synthesis of (+)-Peloruside A Synfacts. 2010: 1331-1331 |
| Ryba TD, Depew KM, Marcaurelle LA. (2009) Large scale preparation of silicon-functionalized SynPhase Polystyrene lanterns for solid-phase synthesis. Journal of Combinatorial Chemistry. 11: 110-6 |
| Hoye TR, Kopel LC, Ryba TD. (2006) In situ generation and nucleophilic capture of 1,n-dial equivalents from 1,n-dioates (α,ω-diesters) Synthesis. 1572-1574 |
| Hoye TR, Ryba TD. (2005) Divergent kinetic control of classical versus ozonolytic lactonization: mechanism-based diastereoselection. Journal of the American Chemical Society. 127: 8256-7 |
| Hoye TR, Aspaas AW, Eklov BM, et al. (2005) Reaction titration: a convenient method for titering reactive hydride agents (Red-Al, LiAlH4, DIBALH, L-Selectride, NaH, and KH) by No-D NMR spectroscopy. Organic Letters. 7: 2205-8 |
| Hoye TR, Eklov BM, Ryba TD, et al. (2004) No-D NMR (no-deuterium proton NMR) spectroscopy: a simple yet powerful method for analyzing reaction and reagent solutions. Organic Letters. 6: 953-6 |