Timothy D. Owens, Ph.D.
Affiliations: | 2002 | University of California, Berkeley, Berkeley, CA, United States |
Area:
chemical synthesisGoogle:
"Timothy Owens"Mean distance: 8.2 | S | N | B | C | P |
Parents
Sign in to add mentor| Jonathan A. Ellman | grad student | 2002 | UC Berkeley | |
| (The design, synthesis, and utility of sulfinyl imine -based ligands for asymmetric catalysis.) | ||||
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Publications
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| Owens TD, Souers AJ, Ellman JA. (2003) The preparation and utility of bis(sulfinyl)imidoamidine ligands for the copper-catalyzed Diels-Alder reaction. The Journal of Organic Chemistry. 68: 3-10 |
| Ellman JA, Owens TD, Tang TP. (2002) N-tert-butanesulfinyl imines: versatile intermediates for the asymmetric synthesis of amines. Accounts of Chemical Research. 35: 984-95 |
| Owens TD, Semple JE. (2001) 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 |
| Souers AJ, Owens TD, Oliver AG, et al. (2001) 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 |
| Owens TD, Hollander FJ, Oliver AG, et al. (2001) 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 |
| Owens TD, Araldi GL, Nutt RF, et al. (2001) Concise total synthesis of the prolyl endopeptidase inhibitor eurystatin A via a novel Passerini reaction-deprotection-acyl migration strategy Tetrahedron Letters. 42: 6271-6274 |
| Semple JE, Owens TD, Nguyen K, et al. (2000) New synthetic technology for efficient construction of alpha-hydroxy-beta-amino amides via the Passerini reaction. Organic Letters. 2: 2769-72 |
| Liu G, Cogan DA, Owens TD, et al. (1999) 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 |
| Owens TD, Semple JE. (1998) 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 |