Year |
Citation |
Score |
2003 |
Owens TD, Souers AJ, Ellman JA. The preparation and utility of bis(sulfinyl)imidoamidine ligands for the copper-catalyzed Diels-Alder reaction. The Journal of Organic Chemistry. 68: 3-10. PMID 12515453 DOI: 10.1021/Jo020524C |
0.647 |
|
2002 |
Ellman JA, Owens TD, Tang TP. N-tert-butanesulfinyl imines: versatile intermediates for the asymmetric synthesis of amines. Accounts of Chemical Research. 35: 984-95. PMID 12437323 DOI: 10.1021/Ar020066U |
0.636 |
|
2001 |
Owens TD, Semple JE. Atom-economical synthesis of the N(10)-C(17) fragment of cyclotheonamides via a novel Passerini reaction-deprotection-acyl migration strategy. Organic Letters. 3: 3301-4. PMID 11594819 DOI: 10.1021/ol0165239 |
0.404 |
|
2001 |
Souers AJ, Owens TD, Oliver AG, Hollander FJ, Ellman JA. Synthesis and crystal structure of a unique and homochiral N,S-bonded N,N'-bis(tert-butanesulfinyl)amidinate rhodium(I) complex. Inorganic Chemistry. 40: 5299-301. PMID 11559098 DOI: 10.1021/Ic0104205 |
0.64 |
|
2001 |
Owens TD, Hollander FJ, Oliver AG, Ellman JA. Synthesis, utility, and structure of novel bis(sulfinyl)imidoamidine ligands for asymmetric Lewis acid catalysis [21] Journal of the American Chemical Society. 123: 1539-1540. DOI: 10.1021/Ja005635C |
0.635 |
|
2001 |
Owens TD, Araldi GL, Nutt RF, Semple JE. Concise total synthesis of the prolyl endopeptidase inhibitor eurystatin A via a novel Passerini reaction-deprotection-acyl migration strategy Tetrahedron Letters. 42: 6271-6274. DOI: 10.1016/S0040-4039(01)01287-4 |
0.435 |
|
2000 |
Semple JE, Owens TD, Nguyen K, Levy OE. New synthetic technology for efficient construction of alpha-hydroxy-beta-amino amides via the Passerini reaction. Organic Letters. 2: 2769-72. PMID 10964361 DOI: 10.1021/Ol0061485 |
0.484 |
|
1999 |
Liu G, Cogan DA, Owens TD, Tang TP, Ellman JA. Synthesis of enantiomerically pure N-tert-butanesulfinyl imines (tert- butanesulfinimines) by the direct condensation of tert-butanesulfinamide with aldehydes and ketones Journal of Organic Chemistry. 64: 1278-1284. DOI: 10.1021/Jo982059I |
0.637 |
|
1998 |
Owens TD, Semple JE. Alkoxide-catalyzed ring-opening of a novel homosaccharin derivative: synthesis of potent, selective P3-lactam thrombin inhibitors containing P4-o-alkoxycarbonylbenzylsulfonamide residues. Bioorganic & Medicinal Chemistry Letters. 8: 3683-8. PMID 9934495 DOI: 10.1016/S0960-894X(98)00667-2 |
0.368 |
|
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