James D. White
Affiliations: | Oregon State University, Corvallis, OR |
Area:
total synthesis of natural productsWebsite:
http://www.chem.orst.edu/white.htmlGoogle:
"James White"Mean distance: 7.52
Parents
Sign in to add mentorGeorge H. Büchi | grad student | 1965 | MIT | |
(A total synthesis of thujopsene: Part I; Metabolites of Penicillium rubrum: Part II.) |
Children
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Publications
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Shaw S, White JD. (2019) Asymmetric Catalysis Using Chiral Salen-Metal Complexes: Recent Advances. Chemical Reviews |
Chen G, Wang R, Vue B, et al. (2018) Optimized synthesis and antiproliferative activity of desTHPdactylolides. Bioorganic & Medicinal Chemistry |
Shaw S, White JD. (2016) cis-2,5-Diaminobicyclo[2.2.2]octane, a New Chiral Scaffold for Asymmetric Catalysis. Accounts of Chemical Research |
Shaw S, White JD. (2016) Asymmetric Catalysis with Iron–Salen Complexes Synthesis (Germany) |
Shaw S, White JD. (2015) Regioselective and Enantioselective Addition of Sulfur Nucleophiles to Acyclic α,β,γ,δ-Unsaturated Dienones Catalyzed by an Iron(III)-Salen Complex. Organic Letters. 17: 4564-7 |
White JD, Li Y, Kim J, et al. (2015) Cyclobutane Synthesis and Fragmentation. A Cascade Route to the Lycopodium Alkaloid (-)-Huperzine A. The Journal of Organic Chemistry |
Suttisintong K, White JD. (2015) Synthesis of two subunits of the macrolide domain of the immunosuppressive agent sanglifehrin a and assembly of a macrolactone precursor. Application of masamune anti-aldol condensation Journal of Organic Chemistry. 80: 2249-2262 |
Shaw S, White JD. (2014) A new iron(III)-salen catalyst for enantioselective Conia-ene carbocyclization. Journal of the American Chemical Society. 136: 13578-81 |
Avery MA, Choudhry SC, Dhingra OP, et al. (2014) Total synthesis of macrodiolide ionophores aplasmomycin A and boromycin via double ring contraction. Organic & Biomolecular Chemistry. 12: 9116-32 |
White JD, Shaw S. (2014) A new cobalt-salen catalyst for asymmetric cyclopropanation. Synthesis of the serotonin-norepinephrine repuptake inhibitor (+)-synosutine Organic Letters. 16: 3880-3883 |