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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)

Thomas R. Hoye

Department of Chemistry

207 Pleasant Street

SE, University of Minnesota




Name/email consistency: high



  • Department of Chemistry, 207 Pleasant Street, SE, University of Minnesota, Minneapolis, USA. 1999 - 2007


  1. Details of the structure determination of the sulfated steroids PSDS and PADS: new components of the sea lamprey (petromyzon marinus) migratory pheromone. Hoye, T.R., Dvornikovs, V., Fine, J.M., Anderson, K.R., Jeffrey, C.S., Muddiman, D.C., Shao, F., Sorensen, P.W., Wang, J. J. Org. Chem. (2007) [Pubmed]
  2. Mosher ester analysis for the determination of absolute configuration of stereogenic (chiral) carbinol carbons. Hoye, T.R., Jeffrey, C.S., Shao, F. Nat. Protoc (2007) [Pubmed]
  3. Silylative Dieckmann-like cyclizations of ester-imides (and diesters). Hoye, T.R., Dvornikovs, V., Sizova, E. Org. Lett. (2006) [Pubmed]
  4. Comparative Diels-Alder reactivities within a family of valence bond isomers: a biomimetic total synthesis of (+/-)-UCS1025A. Hoye, T.R., Dvornikovs, V. J. Am. Chem. Soc. (2006) [Pubmed]
  5. Sequencing of three-component olefin metatheses: total synthesis of either (+)-gigantecin or (+)-14-deoxy-9-oxygigantecin. Hoye, T.R., Eklov, B.M., Jeon, J., Khoroosi, M. Org. Lett. (2006) [Pubmed]
  6. No-D NMR study of the pathway for n-BuLi "oxidation" of 1,5-cyclooctadiene to dilithium cyclooctatetraene dianion [Li2COT2-]. Hoye, T.R., Kabrhel, J.E., Hoye, R.C. Org. Lett. (2005) [Pubmed]
  7. Alkyne haloallylation [with Pd(II)] as a core strategy for macrocycle synthesis: a total synthesis of (-)-haterumalide NA/(-)-oocydin A. Hoye, T.R., Wang, J. J. Am. Chem. Soc. (2005) [Pubmed]
  8. Reaction titration: a convenient method for titering reactive hydride agents (Red-Al, LiAlH4, DIBALH, L-Selectride, NaH, and KH) by No-D NMR spectroscopy. Hoye, T.R., Aspaas, A.W., Eklov, B.M., Ryba, T.D. Org. Lett. (2005) [Pubmed]
  9. Divergent kinetic control of classical versus ozonolytic lactonization: mechanism-based diastereoselection. Hoye, T.R., Ryba, T.D. J. Am. Chem. Soc. (2005) [Pubmed]
  10. No-D NMR (no-deuterium proton NMR) spectroscopy: a simple yet powerful method for analyzing reaction and reagent solutions. Hoye, T.R., Eklov, B.M., Ryba, T.D., Voloshin, M., Yao, L.J. Org. Lett. (2004) [Pubmed]
  11. No-D NMR spectroscopy as a convenient method for titering organolithium (RLi), RMgX, and LDA solutions. Hoye, T.R., Eklov, B.M., Voloshin, M. Org. Lett. (2004) [Pubmed]
  12. Relay ring-closing metathesis (RRCM): a strategy for directing metal movement throughout olefin metathesis sequences. Hoye, T.R., Jeffrey, C.S., Tennakoon, M.A., Wang, J., Zhao, H. J. Am. Chem. Soc. (2004) [Pubmed]
  13. Macrolactonization via Ti(IV)-mediated epoxy-acid coupling: a total synthesis of (-)-dactylolide [and zampanolide]. Hoye, T.R., Hu, M. J. Am. Chem. Soc. (2003) [Pubmed]
  14. A method for easily determining coupling constant values: an addendum to "A practical guide to first-order multiplet analysis in 1H NMR spectroscopy". Hoye, T.R., Zhao, H. J. Org. Chem. (2002) [Pubmed]
  15. Toward computing relative configurations: 16-epi-latrunculin B, a new stereoisomer of the actin polymerization inhibitor latrunculin B. Hoye, T.R., Ayyad, S.E., Eklov, B.M., Hashish, N.E., Shier, W.T., El-Sayed, K.A., Hamann, M.T. J. Am. Chem. Soc. (2002) [Pubmed]
  16. N-methylputrescine oxidation during cocaine biosynthesis: study of prochiral methylene hydrogen discrimination using the remote isotope method. Hoye, T.R., Bjorklund, J.A., Koltun, D.O., Renner, M.K. Org. Lett. (2000) [Pubmed]
  17. Synthesis of a C(1)-C(14)-containing fragment of callipeltoside A. Hoye, T.R., Zhao, H. Org. Lett. (1999) [Pubmed]
  18. An enyne metathesis/(4 + 2)-dimerization route to (+/-)-differolide. Hoye, T.R., Donaldson, S.M., Vos, T.J. Org. Lett. (1999) [Pubmed]
  19. Some allylic substituent effects in ring-closing metathesis reactions: allylic alcohol activation. Hoye, T.R., Zhao, H. Org. Lett. (1999) [Pubmed]
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