| Year |
Citation |
Score |
| 2011 |
Pandya BA, Dandapani S, Duvall JR, Rowley A, Mulrooney CA, Ryba T, Dombrowski M, Harton M, Young DW, Marcaurelle LA. Practical asymmetric synthesis of β-hydroxy γ-amino acids via complimentary aldol reactions. Tetrahedron. 67: 6131-6137. PMID 21822337 DOI: 10.1016/J.Tet.2011.06.043 |
0.436 |
|
| 2010 |
Marcaurelle LA, Comer E, Dandapani S, Duvall JR, Gerard B, Kesavan S, Lee MD, Liu H, Lowe JT, Marie JC, Mulrooney CA, Pandya BA, Rowley A, Ryba TD, Suh BC, et al. 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. PMID 21067169 DOI: 10.1021/Ja105119R |
0.389 |
|
| 2010 |
Hoye TR, Jeon J, Kopel LC, Ryba TD, Tennakoon MA, Wang Y. Total synthesis of peloruside A through kinetic lactonization and relay ring-closing metathesis cyclization reactions. Angewandte Chemie (International Ed. in English). 49: 6151-5. PMID 20645374 DOI: 10.1002/Anie.201002293 |
0.602 |
|
| 2010 |
Hoye T, Jeon J, Kopel L, Ryba T, Tennakoon M, Wang Y. Synthesis of (+)-Peloruside A Synfacts. 2010: 1331-1331. DOI: 10.1055/S-0030-1258876 |
0.585 |
|
| 2009 |
Ryba TD, Depew KM, Marcaurelle LA. Large scale preparation of silicon-functionalized SynPhase Polystyrene lanterns for solid-phase synthesis. Journal of Combinatorial Chemistry. 11: 110-6. PMID 19049425 DOI: 10.1021/Cc8000986 |
0.334 |
|
| 2006 |
Hoye TR, Kopel LC, Ryba TD. In situ generation and nucleophilic capture of 1,n-dial equivalents from 1,n-dioates (α,ω-diesters) Synthesis. 1572-1574. DOI: 10.1055/S-2006-926465 |
0.7 |
|
| 2005 |
Hoye TR, Ryba TD. Divergent kinetic control of classical versus ozonolytic lactonization: mechanism-based diastereoselection. Journal of the American Chemical Society. 127: 8256-7. PMID 15941238 DOI: 10.1021/Ja051604B |
0.58 |
|
| 2005 |
Hoye TR, Aspaas AW, Eklov BM, Ryba TD. 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. PMID 15901170 DOI: 10.1021/Ol0506011 |
0.691 |
|
| 2004 |
Hoye TR, Eklov BM, Ryba TD, Voloshin M, Yao LJ. No-D NMR (no-deuterium proton NMR) spectroscopy: a simple yet powerful method for analyzing reaction and reagent solutions. Organic Letters. 6: 953-6. PMID 15012073 DOI: 10.1021/Ol049979+ |
0.705 |
|
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