Eduardo Torres, Ph.D.
Affiliations: | 2004 | Purdue University, West Lafayette, IN, United States |
Area:
organic synthesisGoogle:
"Eduardo Torres"Mean distance: 8.48 | S | N | B | C | P |
Parents
Sign in to add mentor| Philip L. Fuchs | grad student | 2004 | Purdue | |
| (Functionality propagation of cross -conjugated dienyl sulfones.) | ||||
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Publications
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| Ayala M, Segovia L, Torres E. (2016) Halogenases: A Biotechnological Alternative For The Synthesis Of Halogenated Pharmaceuticals. Mini Reviews in Medicinal Chemistry |
| Pulis AP, Blair DJ, Torres E, et al. (2013) Synthesis of enantioenriched tertiary boronic esters by the lithiation/borylation of secondary alkyl benzoates. Journal of the American Chemical Society. 135: 16054-7 |
| Noshi MN, El-awa A, Torres E, et al. (2007) Conversion of cyclic vinyl sulfones to transposed vinyl phosphonates. Journal of the American Chemical Society. 129: 11242-7 |
| Park T, Torres E, Fuchs PL. (2004) Improved and environmentally friendly large-scale preparation of cyclohexadienyl-, cycloheptadienyl sulfone and enantiopure epoxy cycloheptyl sulfones Synthesis. 1895-1900 |
| Torres E, Chen Y, Kim IC, et al. (2003) Functionality propagation by alkylative oxidation of cross-conjugated cycloheptadienyl sulfones. Angewandte Chemie (International Ed. in English). 42: 3124-31 |
| Chen Y, Evarts JB, Torres E, et al. (2002) Synthesis of termini-differentiated 6-carbon stereotetrads: an alkylative oxidation strategy for preparation of the c21-c26 segment of apoptolidin(1). Organic Letters. 4: 3571-4 |
| Evarts J, Torres E, Fuchs PL. (2002) Syntheses of highly substituted enantiopure C6 and C7 enones(1). Journal of the American Chemical Society. 124: 11093-101 |