Year |
Citation |
Score |
2018 |
Popkin ME, Borman PJ, Omer BA, Seibert KD, Srivastava S, Lepore JV, Hobson L, Donaubauer J, Curran T, Ide N, Tymonko S, Looker A, Kallemeyn JM. The Delivery of Flexibility from the Application of QbD to API Development Journal of Pharmaceutical Innovation. 13: 367-372. DOI: 10.1007/s12247-018-9339-8 |
0.57 |
|
2015 |
Tymonko SA, Smith RC, Ambrosi A, Ober MH, Wang H, Denmark SE. Mechanistic significance of the si-o-pd bond in the palladium-catalyzed cross-coupling reactions of arylsilanolates. Journal of the American Chemical Society. 137: 6200-18. PMID 25945516 DOI: 10.1021/Jacs.5B02518 |
0.613 |
|
2015 |
Tymonko SA, Smith RC, Ambrosi A, Denmark SE. Mechanistic significance of the si-o-pd bond in the palladium-catalyzed cross-coupling reactions of alkenylsilanolates. Journal of the American Chemical Society. 137: 6192-9. PMID 25945390 DOI: 10.1021/Jacs.5B02515 |
0.611 |
|
2007 |
Denmark SE, Smith RC, Tymonko SA. Phosphine Oxides as Stabilizing Ligands for the Palladium-Catalyzed Cross-Coupling of Potassium Aryldimethylsilanolates. Tetrahedron. 63: 5730-5738. PMID 23162169 DOI: 10.1016/J.Tet.2007.02.017 |
0.567 |
|
2006 |
Denmark SE, Neuville L, Christy ME, Tymonko SA. A qualitative examination of the effects of silicon substituents on the efficiency of cross-coupling reactions. The Journal of Organic Chemistry. 71: 8500-9. PMID 17064026 DOI: 10.1021/Jo061481T |
0.429 |
|
2005 |
Denmark SE, Tymonko SA. Sequential cross-coupling of 1,4-bissilylbutadienes: synthesis of unsymmetrical 1,4-disubstituted 1,3-butadienes. Journal of the American Chemical Society. 127: 8004-5. PMID 15926811 DOI: 10.1021/Ja0518373 |
0.442 |
|
2003 |
Denmark SE, Tymonko SA. Cross-coupling of alkynylsilanols with aryl halides promoted by potassium trimethylsilanolate. The Journal of Organic Chemistry. 68: 9151-4. PMID 14604401 DOI: 10.1021/Jo0351771 |
0.459 |
|
2002 |
Gonzalez J, Aurigemma C, Truesdale L, Denmark SE, Tymonko SA, Cottell JJ, Gomez L. Synthesis of (+)-(1S,2R)- and (-)-(! R,2S)-trans-2-phenylcyclohexanol via sharpless asymmetric dihydroxylation (AD) Organic Syntheses. 79: 93-102. |
0.52 |
|
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