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Eduardo Torres, Ph.D. - Publications

Affiliations: 
2004 Purdue University, West Lafayette, IN, United States 
Area:
organic synthesis
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7 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2016 Ayala M, Segovia L, Torres E. Halogenases: A Biotechnological Alternative For The Synthesis Of Halogenated Pharmaceuticals. Mini Reviews in Medicinal Chemistry. PMID 27337971  0.351
2013 Pulis AP, Blair DJ, Torres E, Aggarwal VK. Synthesis of enantioenriched tertiary boronic esters by the lithiation/borylation of secondary alkyl benzoates. Journal of the American Chemical Society. 135: 16054-7. PMID 24138162 DOI: 10.1021/Ja409100Y  0.369
2007 Noshi MN, El-awa A, Torres E, Fuchs PL. Conversion of cyclic vinyl sulfones to transposed vinyl phosphonates. Journal of the American Chemical Society. 129: 11242-7. PMID 17696536 DOI: 10.1021/Ja072890P  0.507
2004 Park T, Torres E, Fuchs PL. Improved and environmentally friendly large-scale preparation of cyclohexadienyl-, cycloheptadienyl sulfone and enantiopure epoxy cycloheptyl sulfones Synthesis. 1895-1900. DOI: 10.1055/S-2004-822318  0.64
2003 Torres E, Chen Y, Kim IC, Fuchs PL. Functionality propagation by alkylative oxidation of cross-conjugated cycloheptadienyl sulfones. Angewandte Chemie (International Ed. in English). 42: 3124-31. PMID 12866097 DOI: 10.1002/Anie.200350955  0.678
2002 Chen Y, Evarts JB, Torres E, Fuchs PL. 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. PMID 12375890 DOI: 10.1021/Ol026377M  0.664
2002 Evarts J, Torres E, Fuchs PL. Syntheses of highly substituted enantiopure C6 and C7 enones(1). Journal of the American Chemical Society. 124: 11093-101. PMID 12224957 DOI: 10.1021/Ja026760M  0.675
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