The Hoye Group at the University of Minnesota

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  1. “Structure assignment through computation of (1H and 13C) NMR chemical shifts: a 'how to' guide for synthetic organic and natural products chemists,” Willoughby, P. H.; Jansma, M. J.; Hoye, T. R. Nature Protocols 2014, 9, 643–660.2014_NMR Nature Protocols Website Abstract.png
  2. “Silicate esters of paclitaxel and docetaxel: synthesis, hydrophobicity, hydrolytic stability, cytotoxicity, and prodrug potential,” Wohl, A. R.; Michel, A. R.; Kalscheuer, S.; Macosko, C. W.; Panyam, J.; Hoye, T. R. J. Med. Chem. 2014, just accepted, xxx–yyy.2014_PTX Silicates JMC Website Abstract.png
  3. “Analysis of seven-membered lactones by computational NMR methods: proton nmr chemical shift data are more discriminating than carbon,” Marell, D. J.; Emond, S. J.; Kulshrestha, A.; Hoye, T. R. J. Org. Chem. 2014, 79, 753–758.2014_Lactones NMR JOC Website Abstract.png
  4. “Cycloaddition reactions of azide, furan, and pyrrole units with benzynes generated by the hexadehydro-Diels-Alder (HDDA) reaction,” Chen, J.; Baire, B.; Hoye, T. R. Heterocycles 2014, 88, 1191–1200.2014_Heterocycles Snieckus Website Abstract.png
  5. “Dichlorination of (HDDA-generated) benzynes and a protocol for interrogating the kinetic order of bimolecular aryne trapping reactions,” Niu, D.; Wang, T.; Woods, B. P.; Hoye, T. R. Org. Lett. 2014, 16, 254–257.2014_Diclorination Website Abstract.png
  6. “Tactics for probing aryne reactivity: mechanistic studies of silicon-oxygen bond cleavage during the trapping of (HDDA-generated) benzynes by silyl ethers,” Baire, B.; Wang, T.; Hoye, T. R. Chem. Sci. 2014, 5, 545–550.2014_Retro-Brook Silicon migration Website Abstract.png
  7. “The aromatic ene reaction,” Niu, D.; Hoye, T. R. Nature Chem. 2014, 6, 34–40.2014_Aromatic ene Website Abstract.png
  1. “Flash nanoprecipitation: particle structure and stability,” Pustulka, K. M.; Wohl, A. R.; Lee, H. S.; Michel, A. R.; Han, J.; Hoye, T. R.; McCormick, A. V.; Macosko, C. W. Pharmaceutics 2013, 10, 4367–4377.2013_FNP Pustulka Website Abstract from Journal.gif
  2. “Alkane desaturation by concerted double hydrogen atom transfer to benzyne,” Niu, D.; Willoughby, P. H.; Baire, B.; Woods, B. P.; Hoye, T. R. Nature 2013, 501, 531–534.2013_H2-Transfer Nautre Eileen Website Abstract.png
  3. “Total synthesis of (±)-leuconolam: intramolecular allylic silane addition to a maleimide carbonyl group,” Izgu, E. C.; Hoye, T. R. Chem. Sci. 2013, 4, 2262–2266.2013_Leuconolam Website Abstract.png
  4. “Polycationic calixarene PTX013, a potent cytotoxic agent against tumors and drug resistant cancer,” Dings, R. P. M.; Levine, J. I.; Astorgues-Xerri, L.; MacDonald, J. R.; Hoye, T. R.; Raymond, E.; Mayo, K. H. Invest. New Drugs 2013, 31, 1142–1150.2013_Calixarene PTX013 Website Abstract.png
  5. “Synthesis of complex benzenoids via the intermediate generation of o-benzynes through the hexadehydro-Diels-Alder reaction,” Baire, B.; Niu, D.; Willoughby, P. H.; Woods, B. P.; Hoye, T. R. Nature Protocols 2013, 8, 501–508.2013_HDDA Nature Protocols Website Abstract.png
  6. “Anti-tumor Agent Calixarene 0118 Targets Human Galectin-1 as an Allosteric Inhibitor of Carbohydrate Binding,” Dings, R. P. M.; Kumar, N.; Miller, M. C.; Loren, M. L.; Rangwala, H.; Hoye, T. R.; Mayo, K. H. J. Pharm. Exp. Ther. 2013, 344, 589–599.2013_6DBF7 Website Abstract.png
  1. “The hexadehydro-Diels–Alder reaction,” Hoye, T. R.; Baire, B.; Niu, D.; Willoughby, P. H.; Woods, B. P. Nature 2012, 490, 208–212.2012_HDDA Nature Website Abstract.png
  2. “Oxyanionic Sigmatropic Rearrangements Relevant to Cyclooctadienone Formation in Penostatins I and F,” Jansma, M. J.; Hoye, T. R. Org. Lett. 2012, 14, 4738–4741.2012_Jansma_Penostatin_Abstract_Resized.png
  3. “Polyurethanes based on renewable polyols from bioderived lactones,” Gurusamy-Thangavelu, S. A.; Emond, S. J.; Kulshrestha, A.; Hillmyer, M. A.; Macosko, C. W.; Tolman, W. B.; Hoye, T. R. Polym. Chem. 2012, 3, 2941–2948.2012_Polymer Chem PU Menthides Website Abstract.png
  4. “Effects of block copolymer properties on nanocarrier protection from in vivo clearance,” D'Addio, S. M.; Saad, W.; Ansell, S. M.; Squiers, J. J.; Adamson, D. H.; Herrera-Alonso, M.; Wohl, A. R.; Hoye, T. R.; Macosko, C. W.; Mayer, L. D.; Vauthier, C.; Prud'homme, R. K. J. Control. Release 2012, 162, 208–217.2012_JCR Controlled Release Prud'homme Website Abstract.png
  5. “o-(Trialkylstannyl)anilines and their utility in Migita-Kosugi-Stille cross-coupling: direct introduction of the 2-aminophenyl substituent,” Izgu, E. C.; Hoye, T. R. Tetrahedron Lett. 2012, 53, 4938–4941.2012_Anilino Stannanes Tet Lett Website Graphic.png
  6. “A simple confined impingement jets mixer for flash nanoprecipitation,” Han, J.; Zhu, Z.; Qian, H.; Wohl, A. R.; Beaman, C. J.; Hoye, T. R.; Macosko, C. W. J. Pharm. Sci. 2012, 101, 4018–4023.2012_CIJ Mixer Website Graphic.png
  7. “A Case Study of Empirical and Computational Chemical Shift Analyses: Reassignment of the Relative Configuration of Phomopsichalasin to that of Diaporthichalasin,” Brown, S. G.; Jansma, M. J.; Hoye, T. R. J. Nat. Prod. 2012, 75, 1326–1331.2012_Diaporthichalasin JNP Website Graphic.png
  8. “Anti-tumor Agent Calixarene 0118 Targets Human Galectin-1 as an Allosteric Inhibitor of Carbohydrate Binding,” Dings, R. P. M.; Nesmelova, I. V.; Astorgues-Xerri, L.; Kumar, N.; Serova, M.; Chen, X.; Raymond, E.; Hoye, T. R.; Mayo, K. H. J. Med. Chem. 2012, 55, 5121–5129.2012_Calixarene 0118 JMC Website Abstract.png
  9. “A Concise Total Synthesis of (±)- and (–)-Okilactomycin D,” Niu, D.; Hoye, T. R. Org. Lett. 2012, 14, 828–831.2012_Okilactomycin Website Abstract.png
  1. “A Strategy for Control of Random Copolymerization of Lactide and Glycolide: Application to Synthesis of PEG-b-PLGA Block Polymers Having Narrow Dispersity,” Qian, H.; Wohl, A. R.; Crow, J. T.; Macosko, C. W.; Hoye, T. R. Macromolecules 2011, 44, 7132–7140.2011_PEG-PLGA Qian Website Abstract.png
  2. “Allylmalonate as an Activator Subunit for the Initiation of Relay Ring-Closing Metathesis Reactions,” Hoye, T. R.; Jeon, J.; Tennakoon, M. A. Angew. Chem. Int. Ed. 2011, 50, 2141–2143.2011_Allyl Malonate RRCM Website Abstract.png
  3. “Access to Functionalized Steroid Side Chains via Modified Julia Olefination,” Izgu, E. C.; Burns, A. C.; Hoye, T. R. Org. Lett. 2011, 13, 703–705.2011_Modified Julla Website Abstract.png
  4. “Synthesis and olfactory activity of unnatural, sulfated 5β-bile acid derivatives in the sea lamprey (Petromyzon marinus),” Burns, A. C.; Sorensen, P. W.; Hoye, T. R. Steroids 2011, 76, 291–300.2011_Steroids Bile Lamptey Website Abstract.png
  1. “Total Synthesis of (–)-Callipeltoside A,” Hoye, T. R.; Danielson, M. E.; May, A. E.; Zhou, H. J. Org. Chem. 2010, 75, 7052–7060 (as a Featured Article).2010_Callipeltoside JOC Website Abstract.png
  2. “Total Synthesis of Peloruside A through Kinetic Lactonization and Relay Ring-Closing Metathesis Cyclization Reactions,” Hoye, T. R.; Jeon, J.; Kopel, L. C.; Ryba, T. D.; Tennakoon, M. A.; Wang, Y. Angew. Chem. Int. Ed. 2010, 49, 6151–6155.2010_Peloruside A ACIE Website Abstract.png
  3. “A useful modification of the Evans magnesium halide catalyzed anti-aldol reaction: application to enolizable aldehydes,” May, A. E.; Connell, N. T.; Dahlmann, H. A.; Hoye, T. R. Synlett 2010, 13, 1984–1986.2010_anti-Aldol Synlett Website Abstract.png
  4. “Room Temperature Acylketene Formation: 1,3-Dioxin-4-ones via Silver(I) Activation of Phenylthioacetoacetate in the Presence of Ketones,” May, A. E.; Hoye, T. R. J. Org. Chem. 2010, 75, 6054–6056.2010_Acylketene Thiolester JOC Website Abstract.png
  5. “Metathesis Involving a Relay and Applications in Natural Product Synthesis,” Hoye, T. R.; Jeon, J. in Metathesis in Natural Product Synthesis: Strategies, Substrates and Catalysts; Cossy, J., Arseniyadis, S., Meyer, C. Ed.; Wiley-VCH: Berlin, 2010, pp 261–285.
  6. “Long-Range Shielding Effects in the 1H NMR Spectra of Mosher-like Ester Derivatives,” Hoye, T. R.; Erickson, S. E.; Erickson-Birkedahl, S. L.; Hale, C. R. H.; Izgu, E. C.; Mayer, M. J.; Notz, P. K.; Renner, M. K. Org. Lett. 2010, 12, 1768–1771.2010_Long-range Mosher Kit Hale Website Abstract.png
  7. “Synthesis of Stable Block-Copolymer-Protected NaYF4:Yb3+, Er3+ Up-Converting Phosphor Nanoparticles,” Budijono, S. J.; Shan, J. N.; Yao, N.; Miura, Y.; Hoye, T. R.; Austin, R. H.; Ju, Y. G.; Prud'homme, R. K. Chem. Materials 2010, 22, 311–318.2010_BlockCopolymerPhosphorNPs.png
  8. “Dynamic Kinetic Resolution During a Vinylogous Payne Rearrangement: A Concise Synthesis of the Polar Pharmacophoric Subunit of (+)-Scyphostatin,” Hoye, T. R.; Jeffrey, C. S.; Nelson, D. P. Org. Lett. 2010, 12, 52–55.2010_DKR OL Website Abstract.png
  1. “Controlled Polymerization of a Cyclic Diene Prepared from the Ring-Closing Metathesis of a Naturally Occurring Monoterpene,” Kobayashi, S.; Lu, C.; Hoye, T. R.; Hillmyer, M. A. J. Am. Chem. Soc. 2009, 131, 7960–7961.2009_Shingo Hllmyer Website Abstract.png
  2. “The evolution of chemistry through synthesis (and of synthesis in chemistry),” Hoye, T. R.; Sizova, E. in Chemical Evolution II; ACS Symposium Series; Friedrich, J., Seidel, R., Zaikowski, L. Ed.; American Chemical Society: Washington, DC, 2009, 1025, pp 181–203
  3. “Maleimide Functionalized Poly(ε-caprolactone)-block-poly(ethylene glycol) (PCL-PEG-MAL): Synthesis, Nanoparticle Formation, and Thiol Conjugation,” Ji, S.; Zhu, Z.; Hoye, T. R.; Macosko, C. W. Macromol. Chem. Phys. 2009, 210, 823–831.2009_MaleimideFuncNPs.jpg
  4. “Okundoperoxide, a bicyclic cyclofarnesylsesquiterpene endoperoxide from Scleria striatinux with antiplasmodial activity,” Efange, A. M. N.; Brun, R.; Wittlin, S.; Connolly, J. D.; Hoye, T. R.; McAkam, T.; Makolo, F. L.; Mbah, J. A.; Nelson, D. P.; Nyongbela, K. D.; Wirmum, C. K. J. Nat. Prod. 2009, 72, 280–283.2009_OkundoperoxideIsolation.gif
  1. “Dual macrolactonization/pyran-hemiketalformation via acylketenes: applications to the synthesis of (–)-callipeltoside A and a lyngbyaloside B model system,” Hoye, T. R.; Danielson, M. E.; May, A. E.; Zhao, H. Angew. Chem. Int. Ed. 2008, 47, 9743–9746.2008_DualMacrolactonizationToCallipeltoside.gif
  2. “Diamino telechelic polybutadienes for solventless styrene-butadiene-styrene (SBS) triblock copolymer formation,” Ji, S.; Hoye, T. R.; Macosko, C. W. Polymer 2008, 49, 5307–5313.2008_SBSTriblockCopolymer.jpg
  3. “Identification of sesquiterpene synthases from Nostoc punctiforme PCC 73102 and Nostoc sp. strain PCC 7120,” Agger, S. A.; Lopez-Gallego, F.; Hoye, T. R.; Schmidt-Dannert, C. J. Bacteriol. 2008, 190, 6084–6096.
  4. “Preparation of Poly(ethylene glycol) Protected Nanoparticles with Variable Bioconjugate Ligand Density,” Gindy, M. E.; Ji, S.; Hoye, T. R.; Panagiotopoulos, A. Z.; Prud'homme, R. K. Biomacromolecules 2008, 9, 2705–2711.2008_PEGProtectedNPs.gif
  5. “New nimbolinin and meliacarpin derivatives from Melia azedarach,” Ayyad, S. N.; Hoye, T. H.; Sreerama, L.; Dawidar, A. M.; Alarif, W. M.; Abdel-Mogib, M. Rev. Lattinoamer. Quim. 2008, 36, 7–15.
  6. “A continuous catalytic system for biodiesel production,” McNeff, C. V.; McNeff, L. C.; Yan, B.; Nowlan, D. T.; Rasmussen, M.; Gyberg, A. E.; Krohn, B. J.; Fedie, R. L.; Hoye, T. R. App. Cat. A.: Gen. 2008, 343, 39–48.2008_McNeff Mcgyan process Website Abstract.png
  7. “Decarboxylative isomerization of N-acyl-2-oxazolidinones to 2-oxazolines,” May, A. E.; Willoughby, P. H.; Hoye, T. R. J. Org. Chem. 2008, 73, 3292–3294.2008_DecarboxyIsomerizationOxazolines.gif
  8. “A thermal decarbonylation of penam β-lactams,” Tian, Z.; Cramer, C. J.; Hoye, T. R. J. Org. Chem. 2008, 73, 3024–3031.2008_ThermalDecarbonylationBetaLactams.gif
  1. “A critical review of the discovery and application of a migratory pheromone in an invasive fish, the sea lamprey Petromyzon marinus L.,” Sorensen, P. W.; Hoye, T. R. J. Fish Biol. 2007, 71 (Suppl. D), 100–114.
  2. “Mosher Ester Analysis for the Determination of Absolute Configuration of Stereogenic (Chiral) Carbinol Carbons,” Hoye, T. R.; Jeffrey, C. S.; Shao, F. Nature Protocols 2007, 2, 2451–2458.
  3. “Formation of Block Copolymer-Protected Nanoparticles via Reactive Impingement Mixing,” Zhu, Z.; Anacker, J. L.; Ji, S.; Hoye, T. R.; Macosko, C. W.; Prud'homme, R. K. Langmuir 2007, 23, 10499–10504.2007_BlockCoPolyImpingmentMixing.gif
  4. “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, 72, 7544–7550.2007_PSDSandPADStrucDetermination.gif
  5. “Comparison of Various Density Functional Methods for Distinguishing Stereoisomers Based on Computed 1H or 13C NMR Chemical Shifts Using Diastereomeric Penam β-Lactams as a Test Set,” Cramer, C. J.; Hoye, T. R. Magn. Reson. Chem. 2007, 45, 819–829.
  6. “Evaluation of various DFT protocols for computing 1H and 13C chemical shifts to distinguish stereoisomers: diastereomeric 2-, 3-, and 4-methylcyclohexanols as a test set,” Al-Rashid, Z. F.; Dvornikovs, V.; Hoye, T. R.; Cramer, C. J. J. Phys. Org. Chem. 2007, 20, 345–354.2007_DFTDiastereomerCyclohexanols.gif
  1. “Trimethyl Phosphonoacetate,” Hoye, T. R.; Sizova, E. e-EROS Encyclopedia of Reagents for Organic Synthesis, First Update 2006.
  2. “Topomimetics of Amphipathic β-Sheet and Helix-Forming Bactericidal Peptides Neutralize Lipopolysaccharide Endotoxins,” Chen, X.; Dings, R. P. M.; Nesmelova, I.; Debbert, S.; Haseman, J. R.; Maxwell, J.; Hoye, T. R.; Mayo, K. H. J. Med. Chem. 2006, 49, 7754–7765.2006_TopomimeticsBactericidalPeptides.gif
  3. “Silylative Dieckmann-Like Cyclizations of Ester-Imides (and Diesters),” Hoye, T. R.; Dvornikovs, V.; Sizova, E. Org. Lett. 2006, 8, 5191–5194.2006_SilylativeDieckmann.gif
  4. “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, 8, 3383–3386.2006_3CompMetathesesGigantecin.gif
  5. “Design of Nonpeptidic Topomimetics of Antiangiogenic Proteins With Antitumor Activities,” Dings, R. P. M.; Chen, X.; Hellebrekers, D. M. E. I.; van Eijk, L. I.; Zhang, Y.; Hoye, T. R.; Griffioen, A. W.; Mayo, K. H. J. Natl. Cancer Inst. 2006, 98, 932–936.
  6. “Hybrid Density Functional Methods Empirically Optimized for the Computation of 13C and 1H Chemical Shifts in Chloroform Solution,” Hoye, T. R.; Cramer, C. J. J. Chem. Theory Comput. 2006, 2, 1085–1092.
  7. In situ generation and nucleophilic capture of 1,n-dialequivalents from 1,n-dioates (α,ω-diesters),” Hoye, T. R.; Kopel, L. C.; Ryba, T. D. Synthesis 2006, 1572–1574.
  8. “Empowerment through ‘Mini-Microscale’ Reactions: The Epoxidation of 1 mg of Geraniol,” Hoye, T. R.; Jeffrey, C. S. J. Chem. Educ. 2006, 83, 919–920.
  9. “Charge storage model for hysteretic negative-differential resistance in metal-molecule-metal junctions,” Kiehl, R. A.; Le, J. D.; Candra, P.; Hoye, R. C.; Hoye, T. R. Appl. Phys. Lett. 2006, 88, 172102/1–172102/3.
  10. “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, 128, 2550–2551.2006_DA_UCS1025A.gif
  1. “Mixture of New Sulfated Steroids Functions as a Migratory Pheromone in the Sea Lamprey,” Sorensen, P. W.; Fine, J. M.; Dvornikovs, V.; Jeffrey, C. S.; Shao, F.; Wang, J.; Vrieze, L. A.; Anderson, K. R.; Hoye, T. R. Nature Chemical Biology 2005, 1, 324–328.2005_SeaLampreyPheremone.gif
  2. “Reactions at polymer–polymer interfaces for blend compatibilization,” Macosko, C. W.; Jeon, H. K.; Hoye, T. R. Prog. Poly. Sci. 2005, 30, 939–947.
  3. “Divergent Kinetic Control of Classical vs. Ozonolytic Lactonization: Mechanism-based Diastereoselection,” Hoye, T. R.; Ryba, T. D. J. Am. Chem. Soc. 2005, 127, 8256–8257.2005_KineticLactonization.gif
  4. “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, 7, 2205–2208.2005_HydrideNoDTitration.gif
  5. “Primary Amine (-NH2) Quantification in Polymers: Functionality by 19F NMR Spectroscopy,” Ji, S.; Macosko, C. W.; Hoye, T. R. Macromolecules 2005, 38, 4679–4686.
  6. “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, 127, 6950–6951.2005_HaterumalideAndOocydinSynthesis.gif
  7. “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, 7, 275–277.2005_NoDOxidationStudyofCyclooctadiene.gif
  8. “A Novel Chemical Route to Stable, Regenerable Zirconia-based Chiral Stationary Phases for HPLC,” Henry, R. A.; McNeff, C. B.; Yan, B.; Hoye, T. R. American Laboratory 2005, 37, 22–24.
  1. “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, 126, 10210–10211.2004_RRCM.gif
  2. “Controlled Synthesis of High Molecular Weight Telechelic Polybutadienes by Ring Opening Metathesis Polymerization,” Ji, S.; Hoye, T. R.; Macosko, C. W. Macromolecules 2004, 37, 5485–5489.
  3. “Coupling Reactions of End- vs Mid-Functional Polymers,” Jeon, J. H.; Macosko, C. W.; Moon, B.; Hoye, T. R.; Yin, Z. Macromolecules 2004, 37, 2563–2571.
  4. “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, 6, 2567–2570.2004_NoDTiteringOrganoLithium.gif
  5. “Synthesis and reactive blending of amine and anhydride end-functional polyolefins,” Jones, T. D.; Macosko, C. W.; Moon, B.; Hoye, T. R. Polymer 2004, 45, 4189–4201.
  6. “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, 6, 953–956.2004_NoDReactionAnalysis.gif
  1. “Negative Differential Resistance in a Bilayer Molecular Junction,” Le, J. D.; He, Y.; Hoye, T. R.; Mead, C. C.; Kiehl, R. A. App. Phys. Lett. 2003, 83, 5518–5520.
  2. “Design of a Partial Peptide Mimetic of Anginex with Antiangiogenic and Anticancer Activity,” Mayo, K. H.; Dings, R. P. M.; Flader, C.; Nesmelova, I.; Hargittai, B.; van der Schaft, D. W. J.; van Eijk, L. I.; Walek, D.; Haseman, J.; Hoye, T. R.; Griffioen, A. W. J. Biol. Chem. 2003, 278, 45746–45752.
  3. “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, 125, 9576–9577.2003_MacrolactonizationTotSynDactylolide.gif
  4. “Cytotoxic Hydroazulene Diterpenes from the Brown Alga Cystoseira myrica,” Ayyad, S. N.; Abdel-Halim, O. B.; Shier, W. T.; Hoye, T. R. Zeitschrift fur Naturforschung C 2003, 58, 33–38.
  1. “Synthesis and Application of Fluorescently Labeled Phthalic Anhydride (PA) Functionalized Polymers by ATRP,” Moon, B.; Hoye, T. R.; Macosko, C. W. Polymer 2002, 43, 5501–5509.
  2. “Toward Computing Relative Configurations: 16-epi-Latrunculin B, a New Stereoisomer of the Actin Polymerization Inhibitor, Latrunculin B,” Hoye, T. R.; Ayyad, S. N.; Eklov, B. M.; Hashish, N. E.; Shier, W. T.; El Sayed, K. A.; Hamann, M. T. J. Am. Chem. Soc. 2002, 124, 7405–7410.2002_ComputingRelConfig_LatrunculinB.gif
  3. “Reactivity of Common Functional Groups with Urethane: Models for Reactive Compatibilization of Thermoplastic Polyurethane Blends,” Lu, Q. W.; Hoye, T. R.; Macosko, C. W. Journal of Polymer Science: Part A: Polymer Chemistry 2002, 40, 2310–2328.
  4. “A Method for Easily Determining Coupling Constant (J) 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, 67, 4014–4016.2002_CouplingConstantAddendum.gif
  1. “Synthesis of end- and mid-Phthalic Anhydride Functional Polymers by Atom Transfer RadicalPolymerization,” Moon, B.; Hoye, T. R.; Macosko, C. W. Macromolecules 2001, 34, 7941–7951.
  2. “A Useful Modification of the Kraus Procedure for Preparation of Ω-Bromo-1-alkenes by HMPA-Promoted Elimination of HBr from 1,Ω-Dibromoalkanes,” Hoye, T. R.; Van Veldhuizen, J. J.; Vos, T. J.; Zhao, P. Synth. Comm. 2001, 31, 1367–1371.
  3. “Synthesis and X-ray Crystallography of Chiral Tropocoronands,” Chenier, P. J.; Halfen, J. A.; Raguse, T. L.; Rich, A. E.; Splan, K. E.; Yoshioka, K.; Hoye, T. R. Synth. Comm. 2001, 31, 487–503.
  1. “Anionic Synthesis and Detection of Fluorescence-labeled Polymers with a Terminal Anhydride Group,” Moon, B.; Hoye, T. R.; Macosko, C. W. J. Polym. Sci., Part A. Polymer Chemistry 2000, 38, 2177–2185.
  2. “Total Synthesis of (–)-Cylindrocyclophane A via a Double Horner-Emmons Macrocyclic Dimerization Event,” Hoye, T. R.; Humpal, P. E.; Moon, B. J. Am. Chem. Soc. 2000, 122, 4982–4983.2000_CylindrocyclophaneSynthesis.gif
  3. “Synthesis (and Alternative Proof of Configuration) of the Scyphostatin C(1')-C(20') Trienoyl Fragment,” Hoye, T. R.; Tennakoon, M. A. Org. Lett. 2000, 2, 1481–1483.2000_ScyphostatinSynthesis.gif
  4. “An NMR Method for Determination of Configuration of β-Substituted Carboxylic Acids,” Hoye, T. R.; Hamad, A. S.; Koltun, D. O.; Tennakoon, M. Tetrahedron Lett. 2000, 41, 2289–2293.
  5. 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, 2, 3–5.2000_N-methylputrescineOxidation.gif
  1. “Some Allylic Substituent Effects in Ring Closing Metathesis Reactions: Allylic Alcohol Activation,” Hoye, T. R.; Zhao, H. Org. Lett. 1999, 1, 1123–1125.1999_AllylicSubstituentEffects.gif
  2. “Total Synthesis of Michellamines A-C, Korupensamines A-D, and Ancistrobrevine B,” Hoye, T. R.; Chen, M.; Hoang, B.; Mi, L.; Priest, O. P. J. Org. Chem. 1999, 64, 7184–7201.1999_MichellamineSynthesis.gif
  3. “An Enyne Metathesis/(4 + 2)-Dimerization Route to (±)-Differolide,” Hoye, T. R.; Donaldson, S. M.; Vos, T. J. Org. Lett. 1999, 1, 277–279.1999_EnyneMetathesisToDifferolide.gif
  4. “Synthesis of a C(1)-C(14) Fragment of Callipeltoside A,” Hoye, T. R.; Zhao, H. Org. Lett. 1999, 1, 169–171.1999_C1C14CallipeltosideASynthesis.gif
  5. “Silicon Tethered Ring-Closing Metathesis Reactions for Self- and Cross-Coupling of Alkenols,” Hoye, T. R.; Promo, M. Tetrahedron Lett. 1999, 40, 1429–1432.1998_SiTetheredRCMAlkenols.gif
  1. “A General, Practical, and Versatile Strategy for Accessing ω-Functional1,2-Diols of High Enantiomeric Excess,” Hoye, T. R.; Mayer, M. J.; Vos, T. J.; Ye, Z. J. Org. Chem. 1998, 63, 8554–8557.
  2. “Otteliones A and B: Potently Cytotoxic 4-Methylene-2-cyclohexenones from Ottelia alismoides,” Ayyad, S-E. N.; Judd, A. S.; Shier, W. T.; Hoye, T. R. J. Org. Chem 1998, 63, 8102–8106.1998_OttelionesAB.gif
  3. “Synthesis of Conformationally Mobile Bicyclic Tetrahydro-1,2-Oxazines by Isomerization of Isoxazolidinylmethyl Tosylates,” Goodwin, T. E.; Cousins, D. M.; Debenham, S. D.; Green, J. L.; Guyer, M. L.; Jacobs, E. G.; Hoye, T. R.; Koltun, D. O.; Vyvyan, J. R. J. Org. Chem. 1998, 63, 4485–4488.
  4. “An NMR Strategy for Determination of Configuration of Remote Stereogenic Centers: 3-Methylcarboxylic Acids,” Hoye, T. R.; Koltun, D. O. J. Am. Chem. Soc. 1998, 120, 4638–4643.
  5. “Amine-Terminal Polystyrenes: A New Strategy for Synthesis and New Methods for Determination of Functionality,” Cernohous, J. J.; Macosko, C. W.; Hoye, T. R. Macromolecules 1998, 31, 3759–3763.
  6. “An Efficient (One-Pot) Synthesis of a New Class of Cyclophanes,” Hoye, T. R.; Cernohous, J. J.; Pfister, K. Tetrahedron Lett. 1998, 39, 1857–1860.1997_OnePotSynthesisCyclophanes.gif
  7. “Synthesis of Azulenone Skeletons by Reaction of 2-Phenyl-2-acylketenes [RCO(Ph)C=C=O] with Alkynyl Ethers: Mechanistic Aspects and Further Transformations,” Brown, D. G.; Hoye, T. R.; Brisbois, R. G. J. Org. Chem. 1998, 63, 1630–1636.
  1. “A Convenient Synthesis of 1-Bromo-4,5-dimethoxy-7-methylnaphthalene, A Naphthol Derivative Useful for Construction of Naphthylisoquinoline Alkaloids,” Hoye, T. R.; Mi, L. J. Org. Chem. 1997, 62, 8586–8588.
  2. “Chiral tropocoronands: Synthesis and metal complex formation,” Chenier, P. J.; Judd, A. S.; Raguse, T. L.; Hoye, T. R. Tetrahedron Lett. 1997, 38, 7341–7344.1997_ChiralTropocoronandsSynthesis.gif
  3. “Anionic Synthesis of Polymers Mono-Functionalized with a Terminal Anhydride Group,” Cernohous, J. J.; Macosko, C. W.; Hoye, T. R. Macromolecules 1997, 30, 5213–5219.
  4. “A Practical Method for Chemoselective Formation of MTPA Amide Derivatives from Amino Alcohols and Phenols,” Hoye, T. R.; Renner, M. K.; Vos-Dinardo, T. J. J. Org. Chem. 1997, 62, 4168–4170.
  1. “Synthesis of the C2-Symmetric, Macrocyclic Alkaloid, (+)-Xestospongin A and its C(9)-Epimer, (-)-Xestospongin C: Impact of Substrate Rigidity and Reaction Conditions on the Efficiency of the Macrocyclic Dimerization Reaction,” Hoye, T. R.; Ye, Z.; Yao, L. J.; North, J. T. J. Am. Chem. Soc. 1996, 118, 12074–12081.
  2. “Applications of MTPA (Mosher) Amides of Secondary Amines: Assignment of Absolute Configuration in Chiral Cyclic Amines,” Hoye, T. R.; Renner, M. K. J. Org. Chem. 1996, 61, 8489–8495.1996_MosherAmidesChiralCyclicAmines.gif
  3. “Studies of Palladium-Catalyzed Cross-Coupling Reactions for Preparation of Highly Hindered Biaryls Relevant to the Korupensamine/Michellamine Problem,” Hoye, T. R.; Chen, M. J. Org. Chem. 1996, 61, 7940–7942.
  4. “Anionic Synthesis, Modification, and Characterization of ABC Triblock Copolymers,” Guégan, P.; Cernohous, J. J.; Khandpur, A. K.; Hoye, T. R.; Macosko, C. W. Macromolecules 1996, 29, 4605–4612.
  5. “Total Synthesis of (ent )-Korupensamine D,” Hoye, T. R.; Chen, M. Tetrahedron Lett. 1996, 37, 3099–3100.1996_TotSynEntKorupensamineD.gif
  6. “Total Syntheses of Korupensamine C and Ancistrobrevine B,” Hoye, T. R.; Mi, L. Tetrahedron Lett. 1996, 37, 3097–3098.1996_TotSynKorupensamineCAncistrobrevineB.gif
  7. “A Convenient Synthesis of Dimethyl (Diazomethyl)phosphonate (Seyferth/Gilbert Reagent),” Brown, D. G.; Velthuisen, E. J.; Commerford, J. R.; Brisbois, R. G.; Hoye, T. R. J. Org. Chem. 1996, 61, 2540–2541.
  8. “MTPA (Mosher) Amides of Cyclic Secondary Amines: Conformational Aspects and a Useful Method for Assignment of Amine Configuration,” Hoye, T. R.; Renner, M. K. J. Org. Chem. 1996, 61, 2056–2064 [Erratum J. Org. Chem. 2006, 71, 1754].1996_MTPAAmideSecondaryAmine.gif
  9. “Enzyme Mediated Synthesis of Stereoisomerically Pure α,ω-Diepoxides,” Hoye, T. R.; Tan, L. Synlett 1996, 615–616.
  10. “A Highly Efficient Synthesis of the Potent Antitumor, C35, Adjacent bis-Tetrahydrofuranyl, Annonaceous Acetogenin, (+)-Parviflorin,” Hoye, T. R.; Ye, Z. J. Am. Chem. Soc. 1996, 118, 1801–1802.
  11. “Intramolecular Cationic Cyclizations Initiated by Electrocyclic Cleavage of Cyclopropanes. Synthesis of Trienic Cyclopentane Derivatives,” Gassman, P. G.; Tan, L.; Hoye, T. R. Tetrahedron Lett. 1996, 37, 439–442.1995_ElectrocyclicCleavageCyclopropane.gif
  1. “Polycyclic Cyclopropanes from Reactions of Alkene-Containing Fischer Carbene Complexes and Alkynes: A Formal Synthesis of (±)-Carabrone,” Hoye, T. R.; Vyvyan, J. R. J. Org. Chem. 1995, 60, 4184–4195.
  2. “Total Synthesis of the Potent Antitumor, bis-Tetrahydrofuranyl Annonaceous Acetogenins (+)-Asimicin and (+)-Bullatacin,” Hoye, T. R.; Tan, L. Tetrahedron Lett. 1995, 36, 1981–1984.1995_TotsynAsimicinBullatacin.gif
  3. “Tandem GC/MS: a Useful Tool for Studying End-Capping Reactions of Oligo(styryl)lithium Anions,” Brestensky, D. M.; Hoye, T. R.; Macosko, C. W. J. Polym. Sci., Part A: Polym. Chem. 1995, 33, 1957–1967.
  1. “Total Synthesis of Michellamines A-C: Important anti-HIV Agents,” Hoye, T. R.; Chen, M.; Mi, L.; Priest, O. Tetrahedron Lett. 1994, 35, 8747–8750.1994_MichellaminesAC.gif
  2. “Stereostructural Studies on the 4-Hydroxylated Annonaceous Acetogenins: A Novel Use of Mosher Ester Data for Determining Relative Configuration [Between C(4) and C(36)],” Hoye, T. R.; Hanson, P. R.; Hasenwinkel, L. E.; Ramirez, E. A.; Zhuang, Z. Tetrahedron Lett. 1994, 35, 8529–8532.1994_AcetogeninsMosherEster.gif
  3. “Stereostructural Studies on the 4-Hydroxylated Annonaceous Acetogenins: Synthesis of Model Butenolides of Known Relative and Absolute Configuration Involving an Intriguing Translactonization Reaction,” Hoye, T. R.; Hanson, P. R.; Hasenwinkel, L. E.; Ramirez, E. A.; Zhuang, Z. Tetrahedron Lett. 1994, 35, 8525–8528.1994_ButenolideTranslactonization.gif
  4. “Relative and Absolute Configuration of the Fumonisin B1 Backbone,” Hoye, T. R.; Jiménez, J. I.; Shier, W. T. J. Am. Chem. Soc. 1994, 116, 9409–9410.
  5. “Conformational Considerations in 1-Oxaquinolizidines Related to the Xestospongin/Araguspongine Family: Reassignment of Stereostructures for Araguspongines B and E,” Hoye, T. R.; North, J. T.; Yao, L. J. J. Org. Chem. 1994, 59, 6904–6910.
  6. “An Efficient and Versatile Synthesis of the Butenolide Subunit of 4-Hydroxylated Annonaceous Acetogenins,” Hoye, T. R.; Humpal, P. E.; Jiménez, J. I.; Mayer, M. J.; Tan, L.; Ye, Z. Tetrahedron Lett. 1994, 35, 7517–7520.1994_ButenolideAcetogenins.gif
  7. “Lithium and Tetramethylammonium Pentacarbonyl (1-Oxidoethylidene)chromate(0) ↔ Acetylpentacarbonylchromate(0) as Acetyl Anion Equivalents for Conjugate Addition Reactions with Electron Deficient Alkenes,” Söderberg, B. C.; York, D. C.; Hoye, T. R.; Rehberg, G. M.; Suriano, J. A. Organometallics 1994, 13, 4501–4509.
  8. “A Practical Guide to First-Order Multiplet Analysis in 1H NMR Spectroscopy,” Hoye, T. R.; Hanson, P. R.; Vyvyan, J. R. J. Org. Chem. 1994, 59, 4096–4103.
  9. “A Total Synthesis of (+)-Xestospongin A/(+)-Araguspongine D,” Hoye, T. R.; North, J. T.; Yao, L. J. J. Am. Chem. Soc. 1994, 116, 2617–2618.
  10. “Enolate and Other Carbon Nucleophile Alkylation Reactions Using Cyclic Sulfates as Epoxide Equivalents,” Hoye, T. R.; Crawford, K. B. J. Org. Chem. 1994, 59, 520–522.
  1. “Synthesis of (-)-Bullatacin: The Enantiomer of a Potent, Antitumor, 4-Hydroxylated Annonaceous, Acetogenin,” Hoye, T. R.; Hanson P, R. Tetrahedron Lett. 1993, 34, 5043–5046.1993_Bullatacin.gif
  2. “Preparation of Fischer Carbene Complexes by Alkylation of Acylmetallates with Alkyl Iodides,” Hoye, T. R.; Chen, K.; Vyvyan, J. R. Organometallics 1993, 12, 2806–2809.
  3. “Cobaltoctacarbonyl Mediated Cyclizations of Electron Deficient Alkynones,” Hoye, T. R.; Suriano, J. A. J. Org. Chem. 1993, 58, 1659–1660.
  4. “A Tungsten[W(CO)5•THF]-Mediated Pauson-Khand Reaction: Cyclizations of 1,6-Enynes via a Batch-Catalytic Protocol,” Hoye, T. R.; Suriano, J. A. J. Am. Chem. Soc. 1993, 115, 1154–1155.
  1. “Determination of Absolute Configuration of Stereogenic Carbinol Centers in Annonaceous Acetogenins by 1H- and 19F-NMR Mosher Ester Analysis,” Rieser, M. J.; Hui, Y.; Rupprecht, J. K.; Kozlowski, J. F.; Wood, K. V.; McLaughlin, J. L.; Hanson, P. R.; Zhuang, Z.; Hoye, T. R. J. Am. Chem. Soc. 1992, 114, 10203–10213.
  2. “A Protecting Group Strategy for Desymmetrization,” Hoye, T. R.; Witowski, N. E. J. Am. Chem. Soc. 1992, 114, 7291–7292.
  3. “Reactions of Pentacarbonyl(1-methoxyethylidene)molybdenum and -tungsten with α,ω-Enynes: Comparison with the Chromium Analog and Resulting Mechanistic Ramifications,” Hoye, T. R.; Suriano, J. A. Organometallics 1992, 11, 2044–2050.
  4. “Tandem Alkyne Insertion and AllylSulfonium Ylide Rearrangement of γ,δ-Alkynyl-α'-Diazoketones,” Hoye, T. R.; Dinsmore, C. J. Tetrahedron Lett. 1992, 33, 169–172.
  1. “Synthesis of (+)-(15,16,19,20,23,24)-hexepi-Uvaricin—a Bistetrahydrofuranyl Annonaceous Acetogenin Analog,” Hoye, T. R.; Hanson, P. R.; Kovelesky, A. C.; Ocain, T. D.; Zhuang, Z. J. Am. Chem. Soc. 1991, 113, 9369–9370.
  2. “Double (Internal/External) Alkyne Insertion Reactions of α-Diazoketones,” Hoye, T. R.; Dinsmore, C. J. Tetrahedron Lett. 1991, 32, 3755–3758.1991_AlkyneInsertReactionsDiazoKetones.gif
  3. “Assigning the Relative Stereochemistry between C(2) and C(4) of the 2-Acetonyl-4-alkylbutyrolactone Substructures of the Pertinent Annonaceous Acetogenins,” Hoye, T. R.; Hanson, P. R. J. Org. Chem. 1991, 56, 5092–5095.
  4. “Rhodium(II) Acetate Catalyzed Alkyne Insertion Reactions of α-Diazoketones: Mechanistic Inferences,” Hoye, T. R.; Dinsmore, C. J. J. Am. Chem. Soc. 1991, 113, 4343–4344.
  1. “Manganese Fischer carbene chemistry: Reactions of Cp'(CO)2Mn=C(OMe/OLi)R with Enynes, 1-Hexyne, and Acrylates,” Hoye, T. R.; Rehberg, G. M. Organometallics 1990, 9, 3014–3015.
  2. “Thermodynamic Control of Stereochemistry in the Synthesis of 1-Oxaquinolizidine Skeletal Portions of Xestospongin A,” Hoye, T. R.; North, J. T. Tetrahedron Lett. 1990, 31, 4281–4284.1990_ThermoControlXestosponginA.gif
  3. “Alkyne Insertion Reactions of Metal-carbenes Derived from Enynyl-α-diazoketones [R'CN2COCR2CH2C≡C(CH2)n-2CH=CH2],” Hoye, T. R.; Dinsmore, C. J.; Johnson, D. S.; Korkowski, P. F. J. Org. Chem. 1990, 55, 4518–4520.
  4. “1-Oxyalkylidenepentacarbonylchromium Anion [R(O-)C=Cr(CO)5] ↔ Acylpentacarbonyl-chromate [acyl-Cr-(CO)5] Chemistry: In Situ Preparation and Reactions with Alkynes and Enynes,” Hoye, T. R.; Rehberg, G. M. J. Am. Chem. Soc. 1990, 112, 2841–2842.
  1. “(1-Pyrrolidinoethylidene)pentacarbonyl Chromium Mediated Conversion of Enynes to Bicyclic, Cyclopropane-Containing Carbon Skeletons: Donor Group Effects,” Hoye, T. R.; Rehberg, G. M. Organometallics 1989, 8, 2070–2071.
  2. “A Short, Oxetane-based Synthesis of (±)-Sarracenin,” Hoye, T. R.; Richardson, W. S. J. Org. Chem. 1989, 54, 688–693.
  1. “Validation of the 1H NMR Chemical Shift Method for Determination of Stereochemistry in the Bistetrahydrofuranyl Moiety of Uvaricin-related Acetogenins from Annonaceae : Rolliniastatin 1 (and Asimicin),” Hoye, T. R.; Zhuang, Z. P. J. Org. Chem. 1988, 53, 5578–5580.
  2. “Fischer Carbene Mediated Conversions of Enynes to Bi- and Tricyclic Cyclopropane-containing Carbon Skeletons,” Korkowski, P. F.; Hoye, T. R.; Rydberg, D. B. J. Am. Chem. Soc. 1988, 110, 2676–2678.
  1. “Asymmetric Synthesis of Achiral Molecules: Meso Selectivity,” Hoye, T. R.; Jenkins, S. A. J. Am. Chem. Soc. 1987, 109, 6196–6198 (reviewed in inaugural issue of Chemtracts 1988, 1, 29).
  2. “On the Stereochemistry of the Bistetrahydrofuranyl Moiety of Uvaricin: Proton NMR Chemical Shifts Can Play a Crucial Role in Structure Determination,” Hoye, T. R.; Suhadolnik, J. C. J. Am. Chem. Soc. 1987, 109, 4402–4403.
  3. “Preparation of 5-Alkyl-2-t-butyl-1,3-dioxolanones by Trimethylsilyl Triflate Catalyzed Reactions Between Bis-Trimethylsilyl Derivatives of α-Hydroxycarboxylic Acids and Pivaldehyde,” Hoye, T. R.; Peterson, B. H.; Miller, J. D. J. Org. Chem. 1987, 52, 1351–1353.
  1. “Stereocontrolled Synthesis of 2,5-Linked Bistetrahydrofurans via the Triepoxide Cascade Reaction,” Hoye, T. R.; Suhadolnik, J. C. Tetrahedron (Symposium in Print) 1986, 42, 2855–2862.
  1. “Amidoacetone Enolate Anions: Alkylation and Michael Reaction,” Hoye, T. R.; Duff, S. R.; King, R. S. Tetrahedron Lett. 1985, 26, 3433–3436.
  2. “Symmetry-Assisted Synthesis of Triepoxide Stereoisomers of (E,Z,E,)-Dodeca-2,6,10-triene-1,12-diol and Their Cascade Reactions to 2,5-Linked Bistetrahydrofurans,” Hoye, T. R.; Suhadolnik, J. C. J. Am. Chem. Soc. 1985, 107, 5312–5313.
  1. “Kinetic Lactonization of 4,6-Dimethyl- and 2,4,6,8-Tetramethyl-5-hydroxy Azelaic Acids: Ground-State Conformational Control,” Hoye, T. R.; Peck, D. R.; Swanson, T. A. J. Am. Chem. Soc. 1984, 106, 2738–2739.
  2. In Situ Preparation and Fate of cis-4-Hydroxycyclophosphamide and Aldophosphamide: 31P NMR Evidence for Equilibration of cis-and trans-Hydroxycyclophosphamide with Aldophosphamide and its Hydrate in Aqueous Solution,” Borch, R. F.; Hoye, T. R.; Swanson, T. A. J. Med. Chem. 1984, 27, 490–494.
  3. “Stereochemistry of ethyl 2,6-dimethyl-4-oxo-2-cyclohexenecarboxylate (6-methyl Hagemann's ester) and its products of conjugate addition by vinylmagnesium bromide/copper(I) iodide,” Hoye, T. R.; Magee, A. S.; Rosen, R. E. J. Org. Chem. 1984, 27, 3224–3226.
  1. “Preparation of d,l-Megaphone Intermediates,” Hoye, T. R.; Kurth, M. J. Tetrahedron Lett. 1983, 24, 4769–4772.
  1. “Preparation and Diels-Alder Reactions of 1,1-Dicarbonylalkenes,” Hoye, T. R.; Caruso, A. J.; Magee, A. S. J. Org. Chem. 1982, 47, 4152–4156.
  2. “Two Syntheses of d,l-Aplysistatin,” Hoye, T. R.; Caruso, A. J.; Dellaria, J. F., Jr.; Kurth, M. J. J. Am. Chem. Soc. 1982, 104, 6704–6709.
  3. “3,5-Hexadienoic Esters: A Convenient Preparation,” Hoye, T. R.; Magee, A. S.; Trumper, W. S. Syn Comm. 1982, 12, 183–187.
  4. “3,4,5-Trimethoxyphenyllithium,” Hoye, T. R.; Kaese, P. A. Syn. Comm. 1982, 12, 49–52.
  5. “Intramolecular Photochemical Cycloaddition Reactions of 3-(1,5-Dimethylhex-4-enyl)cyclohex-2-enone: Regio- and Stereochemical Aspects,” Hoye, T. R.; Martin, S. J.; Peck, D. R. J. Org. Chem. 1982, 48, 331–337.
  1. “Symmetry in Synthesis. Preparation and Methylation of Spiro Dilactones,” Hoye, T. R.; Peck, D. R.; Trumper, P. K. J. Am. Chem. Soc. 1981, 103, 5618–5620.
  2. “Internal Nucleophilic Termination in Mercuric Ion Initiated Diene Cyclizations,” Hoye, T. R.; Caruso, A. J.; Kurth, M. J. J. Org. Chem. 1981, 46, 3550–3552.
  3. “Steric Impedence in the 1,3-Photocycloaddition Reaction Between Cyclopentene and Anisole Derivatives,” Hoye, T. R. Tetrahedron Lett. 1981, 22, 2523–2526.
  4. “Triphenylcarbenium and Tris(p-bromophenyl)ammoniumyl Ion Induced Lactonizations of α,ω-p-Methoxybenzyloxy Methyl Esters,” Hoye, T. R.; Kurth, M. J.; Lo, V. Tetrahedron Lett. 1981, 22, 815–818.
  5. “Total Synthesis of d,l-Ancistrofuran: A Study of Cyclic Ether Formation,” Hoye, T. R.; Caruso, A. J. J. Org. Chem. 1981, 46, 1198–1205.
  1. “Regio- and Stereoselectivity in the Ene Reaction of N-Phenyl-1,2,4-triazoline-3,5-dione with α,β-Unsaturated Carbonyl Substrates,” Hoye, T. R.; Bottorff, K. J.; Caruso, A. J.; Dellaria, J. F., Jr. J. Org. Chem. 1980, 45, 4287–4292.
  2. “Preparation of β-Hydroxy-α-phenylthioesters via Condensation of Aldehydes with α-Phenylthioester Enolate Anions,” Hoye, T. R.; Kurth, M. J. J. Org. Chem. 1980, 45, 3549–3554.
  1. “Total Synthesis of d,l-Aplysistatin,” Hoye, T. R.; Kurth, M. J. J. Am. Chem. Soc. 1979, 101, 5065–5067.
  2. “Mercuric Trifluoroacetate Mediated Brominative Cyclizations of Dienes: Total Synthesis of d,l-3β-Bromo-8-epicaparrapi Oxide,” Hoye, T. R.; Kurth, M. J. J. Org. Chem. 1979, 44, 3461–3467.
  3. “Mercuric Acetate Oxidation of 1-Vinylcycloalkenes: Diels-Alder Reactivity of Resultant Allylic Diene Acetates,” Hoye, T. R.; Rother, M. J. J. Org. Chem. 1979, 44, 458–461.
  1. “A 1,3-Diene-2-Carboxylic Ester Synthesis: Reaction of Alkylidene-γ-lactones with Potassium and Sodium PhenylSelenoate,” Hoye, T. R.; Caruso, A. J. Tetrahedron Lett. 1978, 4611–4614.
  2. “Brominative Cyclizations of Geranyl Derivatives,” Hoye, T. R.; Kurth, M. J. J. Org. Chem. 1978, 43, 3693–3697.
  1. “Total Synthesis of Illudinine, Illudalic Acid, and Illudacetallic Acid,” Woodward, R. B.; Hoye, T. R. J. Am. Chem. Soc. 1977, 99, 8007–8014.
  1. “Diaziridines II. The Addition of Diaziridines to Electrophilic Acetylenes,” Heine, H. W.; Hoye, T. R.; Williard, P. G.; Hoye, R. C. J. Org. Chem. 1973, 38, 2984–2988.
  1. “The Synthesis and Reactions of Some 1-(Nitroaryl)diaziridines,” Heine, H. W.; Williard, P. G.; Hoye, T. R. J. Org. Chem. 1972, 37, 2980–2983.