| Year |
Citation |
Score |
| 2023 |
Kaicharla T, Lee S, Wang R, Pehere AD, Xu S, Hoye TR. Novel Conversions of a Multifunctional, Bio-sourced Lactone Carboxylic Acid. Arkivoc : Free Online Journal of Organic Chemistry. 2. PMID 38361761 DOI: 10.24820/ark.5550190.p012.081 |
0.336 |
|
| 2023 |
Kraemer N, Eason EM, Hoye TR. Intramolecular Cyclization of Alkynylheteroaromatic Substrates Bearing a Tethered Cyano Group: A Strategy for Accessing Fused Pyridoheterocycles. The Journal of Organic Chemistry. 88: 12716-12726. PMID 37590897 DOI: 10.1021/acs.joc.3c01411 |
0.336 |
|
| 2022 |
Kaicharla T, Chinta BS, Hoye TR. Examples Showing the Utility of Doping Experiments in H NMR Analysis of Mixtures. The Journal of Organic Chemistry. PMID 35442679 DOI: 10.1021/acs.joc.1c03127 |
0.754 |
|
| 2022 |
Kraemer N, Naredla RR, Hoye TR. In Situ Allene Formation via Alkyne Tautomerization to Promote [4 + 2]-Cycloadditions with a Pendant Alkyne or Nitrile. Organic Letters. 24: 2327-2331. PMID 35311283 DOI: 10.1021/acs.orglett.2c00491 |
0.816 |
|
| 2022 |
Haque FM, Ishibashi JSA, Lidston CAL, Shao H, Bates FS, Chang AB, Coates GW, Cramer CJ, Dauenhauer PJ, Dichtel WR, Ellison CJ, Gormong EA, Hamachi LS, Hoye TR, Jin M, et al. Defining the Macromolecules of Tomorrow through Synergistic Sustainable Polymer Research. Chemical Reviews. PMID 35133803 DOI: 10.1021/acs.chemrev.1c00173 |
0.35 |
|
| 2022 |
Chinta BS, Arora S, Hoye TR. Trapping Reactions of Benzynes Initiated by Intramolecular Nucleophilic Addition of a Carbonyl Oxygen to the Electrophilic Aryne. Organic Letters. 24: 425-429. PMID 34958573 DOI: 10.1021/acs.orglett.1c04110 |
0.82 |
|
| 2021 |
Lee D, Ross SP, Xiao X, Hoye TR. Radial hexadehydro-Diels-Alder reactions. Chem. 7: 2527-2537. PMID 35097238 DOI: 10.1016/j.chempr.2021.08.010 |
0.47 |
|
| 2021 |
Lynn M, Pierson Smela M, Hoye TR. Silicon as a powerful control element in HDDA chemistry: redirection of innate cyclization preferences, functionalizable tethers, and formal bimolecular HDDA reactions. Chemical Science. 12: 13902-13908. PMID 34760176 DOI: 10.1039/d1sc04082k |
0.313 |
|
| 2021 |
Zhu C, Zhang J, Hoye TR. Assembly of the Benzenoid Ring as a Core Strategy for Synthesis of the Isoindolinone Natural Products Isohericerin, Erinacerin A, and Sterenin A. Organic Letters. PMID 34543031 DOI: 10.1021/acs.orglett.1c02752 |
0.338 |
|
| 2021 |
Guptill DM, Chinta BS, Kaicharla T, Xu S, Hoye TR. β-Methyl-δ-valerolactone-containing Thermoplastic Poly(ester-amide)s: Synthesis, Mechanical Properties, and Degradation Behavior. Polymer Chemistry. 12: 1310-1316. PMID 34354765 DOI: 10.1039/d1py00040c |
0.798 |
|
| 2021 |
Arora S, Hoye TR. "Kobayashi Benzynes" as Hexadehydro-Diels-Alder Diynophiles. Organic Letters. PMID 33884877 DOI: 10.1021/acs.orglett.1c00787 |
0.734 |
|
| 2021 |
Chinta BS, Lee D, Hoye TR. Coumarin (5,6-Benzo-2-pyrone) Trapping of an HDDA-Benzyne. Organic Letters. PMID 33650870 DOI: 10.1021/acs.orglett.1c00342 |
0.788 |
|
| 2021 |
Fluegel LL, Hoye TR. Hexadehydro-Diels-Alder Reaction: Benzyne Generation via Cycloisomerization of Tethered Triynes. Chemical Reviews. PMID 33492939 DOI: 10.1021/acs.chemrev.0c00825 |
0.338 |
|
| 2020 |
Arora S, Sneddon DS, Hoye TR. Reactions of HDDA Benzynes with -Diarylimines (ArCH=NAr'). European Journal of Organic Chemistry. 2020: 2379-2383. PMID 33776554 DOI: 10.1002/Ejoc.201901855 |
0.772 |
|
| 2020 |
Xu S, Wang Y, Hoye TR. Poly(4-ketovalerolactone) from Levulinic acid: Synthesis and Hydrolytic Degradation. Macromolecules. 53: 4952-4959. PMID 33767514 DOI: 10.1021/Acs.Macromol.0C00787 |
0.373 |
|
| 2020 |
Lopes DT, Hoye TR, Alvarenga ES. Characterization of stereoisomeric 5-(2-nitro-1-phenylethyl)furan-2(5H)-ones by computation of H and C NMR chemical shifts and electronic circular dichroism spectra. Magnetic Resonance in Chemistry : Mrc. PMID 32621355 DOI: 10.1002/Mrc.5073 |
0.362 |
|
| 2020 |
Anantharamkrishnan V, Hoye T, Reineccius GA. Covalent Adduct Formation Between Flavor Compounds of Various Functional Group Classes and the Model Protein β-Lactoglobulin. Journal of Agricultural and Food Chemistry. 68: 6395-6402. PMID 32390422 DOI: 10.1021/Acs.Jafc.0C01925 |
0.347 |
|
| 2020 |
Willoughby PH, Jansma MJ, Hoye TR. Addendum: A guide to small-molecule structure assignment through computation of (¹H and ¹³C) NMR chemical shifts. Nature Protocols. PMID 31949288 DOI: 10.1038/s41596-020-0293-9 |
0.769 |
|
| 2019 |
Arora S, Zhang J, Pogula V, Hoye TR. Reactions of thermally generated benzynes with six-membered -heteroaromatics: pathway and product diversity. Chemical Science. 10: 9069-9076. PMID 31827748 DOI: 10.1039/C9Sc03479J |
0.813 |
|
| 2019 |
Thompson SK, Hoye TR. The Aza-hexadehydro-Diels-Alder Reaction. Journal of the American Chemical Society. PMID 31789026 DOI: 10.1021/Jacs.9B11243 |
0.472 |
|
| 2019 |
Xiao X, Hoye TR. A One-pot, Three-Aryne Cascade Strategy for Naphthalene Formation from 1,3-Diynes and 1,2-Benzdiyne Equivalents. Journal of the American Chemical Society. PMID 31181885 DOI: 10.1021/Jacs.9B04606 |
0.527 |
|
| 2019 |
Zhang J, Hoye TR. Divergent Reactivity during the Trapping of Benzynes by Glycidol Analogs: Ring Cleavage via Pinacol-Like Rearrangements vs Oxirane Fragmentations. Organic Letters. PMID 30969776 DOI: 10.1021/Acs.Orglett.9B00595 |
0.416 |
|
| 2019 |
Shen H, Xiao X, Hoye TR. Benzyne Cascade Reactions via Benzoxetenonium Ions and Their Rearrangements to o-Quinone Methides. Organic Letters. PMID 30829492 DOI: 10.1021/Acs.Orglett.9B00215 |
0.506 |
|
| 2019 |
Neitzel AE, Barreda L, Trotta JT, Fahnhorst GW, Haversang TJ, Hoye TR, Fors BP, Hillmyer MA. Hydrolytically-degradable homo- and copolymers of a strained exocyclic hemiacetal ester Polymer Chemistry. 10: 4573-4583. DOI: 10.1039/C9Py00797K |
0.327 |
|
| 2018 |
Arora S, Palani V, Hoye TR. Reactions of Diaziridines with Benzynes Give N-Arylhydrazones. Organic Letters. PMID 30532977 DOI: 10.1021/Acs.Orglett.8B03439 |
0.745 |
|
| 2018 |
Wang Y, Zheng L, Hoye TR. Sulfonamide-Trapping Reactions of Thermally Generated Benzynes. Organic Letters. 20: 7145-7148. PMID 30394095 DOI: 10.1021/Acs.Orglett.8B03085 |
0.36 |
|
| 2018 |
Xiao X, Wang T, Xu F, Hoye TR. Cu(I)-Mediated Bromoalkynylation and Hydroalkynylation Reactions of Unsymmetrical Benzynes: Complementary Modes of Addition. Angewandte Chemie (International Ed. in English). PMID 30390400 DOI: 10.1002/Anie.201811783 |
0.487 |
|
| 2018 |
Shen H, Xiao X, Haj MK, Willoughby PH, Hoye TR. BF3-Promoted, Carbene-like, C-H Insertion Reactions of Benzynes. Journal of the American Chemical Society. PMID 30384597 DOI: 10.1021/Jacs.8B10206 |
0.78 |
|
| 2018 |
Zhang J, Page ACS, Palani V, Chen J, Hoye TR. Atypical Mode of [3 + 2]-Cycloaddition: Pseudo-1,3-dipole Behavior in Reactions of Electron-Deficient Thioamides with Benzynes. Organic Letters. PMID 30156418 DOI: 10.1021/Acs.Orglett.8B02133 |
0.359 |
|
| 2018 |
Smela MP, Hoye TR. A Traceless Tether Strategy for Achieving Formal Intermolecular Hexadehydro-Diels-Alder Reactions. Organic Letters. PMID 30125112 DOI: 10.1021/Acs.Orglett.8B02473 |
0.446 |
|
| 2018 |
Xiao X, Hoye TR. The domino hexadehydro-Diels-Alder reaction transforms polyynes to benzynes to naphthynes to anthracynes to tetracynes (and beyond?). Nature Chemistry. 10: 838-844. PMID 30030536 DOI: 10.1038/S41557-018-0075-Y |
0.534 |
|
| 2018 |
Wang Y, Hoye TR. Isomerizations of Propargyl 3-Acylpropiolates via Reactive Allenes. Organic Letters. PMID 29999326 DOI: 10.1021/Acs.Orglett.8B01705 |
0.406 |
|
| 2018 |
Hoye TR, Xiao X, Woods BP. Benzocyclobutadienes: An unusual mode of access reveals unusual modes of reactivity. Angewandte Chemie (International Ed. in English). PMID 29874408 DOI: 10.1002/Anie.201803872 |
0.773 |
|
| 2018 |
Fahnhorst GW, Stasiw DE, Tolman WB, Hoye TR. Isomerization of Linear to Hyperbranched Polymers: Two Isomeric Lactones Converge via Metastable Isostructural Polyesters to a Highly Branched Analogue Acs Macro Letters. 7: 1144-1148. DOI: 10.1021/Acsmacrolett.8B00621 |
0.353 |
|
| 2018 |
Fahnhorst GW, Hoye TR. A Carbomethoxylated Polyvalerolactone from Malic Acid: Synthesis and Divergent Chemical Recycling Acs Macro Letters. 7: 143-147. DOI: 10.1021/Acsmacrolett.7B00889 |
0.341 |
|
| 2017 |
Wang Y, Hoye TR. Intramolecular Capture of HDDA-Derived Benzynes: (i) 6- to 12-Membered Ring Formation, (ii) Internally (vis-à-vis Remotely) Tethered Traps, and (iii) Role of the Rate of Trapping by the Benzynophile. Organic Letters. PMID 29244510 DOI: 10.1021/Acs.Orglett.7B03436 |
0.367 |
|
| 2017 |
Ross SP, Hoye TR. Multiheterocyclic Motifs via Three-Component Reactions of Benzynes, Cyclic Amines, and Protic Nucleophiles. Organic Letters. PMID 29239617 DOI: 10.1021/Acs.Orglett.7B03458 |
0.455 |
|
| 2017 |
Ross SP, Baire B, Hoye TR. Mechanistic Duality in Tertiary Amine Additions to Thermally Generated Hexadehydro-Diels-Alder Benzynes. Organic Letters. PMID 28981290 DOI: 10.1021/Acs.Orglett.7B02888 |
0.692 |
|
| 2017 |
Li K, Scott AM, Brant CO, Fissette SD, Riedy JJ, Hoye TR, Li W. Bile Salt-like Dienones Having a Novel Skeleton or a Rare Substitution Pattern Function as Chemical Cues in Adult Sea Lamprey. Organic Letters. PMID 28816048 DOI: 10.1021/Acs.Orglett.7B01921 |
0.317 |
|
| 2017 |
Thompson SK, Hoye TR. Organic chemistry: Molecular structure assignment simplified. Nature. 547: 410-411. PMID 28748936 DOI: 10.1038/547410A |
0.329 |
|
| 2017 |
Xu F, Xiao X, Hoye TR. The Photochemical Hexadehydro-Diels-Alder (hv-HDDA) Reaction. Journal of the American Chemical Society. PMID 28548500 DOI: 10.1021/Jacs.7B03832 |
0.53 |
|
| 2017 |
Ross SP, Hoye TR. Reactions of hexadehydro-Diels-Alder benzynes with structurally complex multifunctional natural products. Nature Chemistry. 9: 523-530. PMID 28537589 DOI: 10.1038/Nchem.2732 |
0.45 |
|
| 2017 |
Wang T, Oswood CJ, Hoye TR. Trapping of Hexadehydro-Diels–Alder Benzynes with Exocyclic, Conjugated Enals as a Route to Fused Spirocyclic Benzopyran Motifs Synlett. 28: 2933-2935. DOI: 10.1055/S-0036-1589091 |
0.368 |
|
| 2017 |
Guptill DM, Brutman JP, Hoye TR. Thermoplastic polyurethanes from β-methyl-δ-valerolactone-derived amidodiol chain extenders Polymer. 111: 252-257. DOI: 10.1016/J.Polymer.2017.01.042 |
0.741 |
|
| 2016 |
Palani V, Chen J, Hoye TR. Reactions of Hexadehydro-Diels-Alder (HDDA)-Derived Benzynes with Thioamides: Synthesis of Dihydrobenzothiazino-Heterocyclics. Organic Letters. 18: 6312-6315. PMID 27978648 DOI: 10.1021/Acs.Orglett.6B03199 |
0.379 |
|
| 2016 |
Ball-Jones NR, Fahnhorst GW, Hoye TR. Poly(isoprenecarboxylates) from Glucose via Anhydromevalonolactone. Acs Macro Letters. 5: 1128-1131. PMID 27933217 DOI: 10.1021/Acsmacrolett.6B00560 |
0.788 |
|
| 2016 |
Zhang J, Niu D, Brinker VA, Hoye TR. The Phenol-Ene Reaction: Biaryl Synthesis via Trapping Reactions between HDDA-Generated Benzynes and Phenolics. Organic Letters. PMID 27767316 DOI: 10.1021/Acs.Orglett.6B02830 |
0.63 |
|
| 2016 |
Xu F, Xiao X, Hoye TR. Reactions of HDDA-Derived Benzynes with Perylenes: Rapid Construction of Polycyclic Aromatic Compounds. Organic Letters. PMID 27766886 DOI: 10.1021/Acs.Orglett.6B02878 |
0.529 |
|
| 2016 |
Wang T, Hoye TR. Hexadehydro-Diels-Alder (HDDA)-Enabled Carbazolyne Chemistry: Single Step, de Novo Construction of the Pyranocarbazole Core of Alkaloids of the Murraya koenigii (Curry Tree) Family. Journal of the American Chemical Society. PMID 27734671 DOI: 10.1021/Jacs.6B09628 |
0.44 |
|
| 2016 |
Xu F, Hershey KW, Holmes RJ, Hoye TR. Blue-emitting Arylalkynyl Naphthalene Derivatives via a Hexadehydro-Diels-Alder (HDDA) Cascade Reaction. Journal of the American Chemical Society. PMID 27626808 DOI: 10.1021/Jacs.6B07647 |
0.368 |
|
| 2016 |
Wang T, Niu D, Hoye TR. The hexadehydro-Diels-Alder (HDDA) cycloisomerization reaction proceeds by a stepwise mechanism. Journal of the American Chemical Society. PMID 27266843 DOI: 10.1021/Jacs.6B03786 |
0.586 |
|
| 2016 |
Pehere AD, Xu S, Thompson SK, Hillmyer MA, Hoye TR. Diels-Alder Reactions of Furans with Itaconic Anhydride: Overcoming Unfavorable Thermodynamics. Organic Letters. PMID 27214494 DOI: 10.1021/Acs.Orglett.6B00929 |
0.816 |
|
| 2016 |
Wang T, Naredla RR, Thompson SK, Hoye TR. The pentadehydro-Diels-Alder reaction. Nature. PMID 27088605 DOI: 10.1038/Nature17429 |
0.815 |
|
| 2016 |
Chen J, Palani V, Hoye TR. Reactions of HDDA-derived Benzynes with Sulfides: Mechanism, Modes, and Three-component Reactions. Journal of the American Chemical Society. PMID 27010747 DOI: 10.1021/Jacs.6B01025 |
0.448 |
|
| 2016 |
Wang T, Naredla RR, Thompson SK, Hoye TR. ChemInform Abstract: The Pentadehydro-Diels-Alder Reaction. Cheminform. 47. DOI: 10.1002/chin.201635093 |
0.812 |
|
| 2015 |
Hoye TR, Alarif WM, Basaif SS, Abo-Elkarm M, Hamann MT, Wahba AE, Ayyad SN. New cytotoxic cyclic peroxide acids from Plakortis sp. marine sponge. Arkivoc : Free Online Journal of Organic Chemistry / Arkat-Usa, Inc. 2015: 164-175. PMID 26835518 DOI: 10.3998/Ark.5550190.P008.948 |
0.307 |
|
| 2015 |
Han J, Michel AR, Lee HS, Kalscheuer S, Wohl A, Hoye TR, McCormick AV, Panyam J, Macosko CW. Nanoparticles Containing High Loads of Paclitaxel-Silicate Prodrugs: Formulation, Drug Release, and Anticancer Efficacy. Molecular Pharmaceutics. PMID 26505116 DOI: 10.1021/Acs.Molpharmaceut.5B00530 |
0.647 |
|
| 2015 |
Marell DJ, Furan LR, Woods BP, Lei X, Bendelsmith AJ, Cramer CJ, Hoye TR, Kuwata KT. Mechanism of the Intramolecular Hexadehydro-Diels-Alder Reaction. The Journal of Organic Chemistry. PMID 26270857 DOI: 10.1021/Acs.Joc.5B01356 |
0.81 |
|
| 2015 |
Wang T, Hoye TR. Diels-Alderase-free, bis-pericyclic, [4+2] dimerization in the biosynthesis of (±)-paracaseolide A. Nature Chemistry. 7: 641-5. PMID 26201740 DOI: 10.1038/Nchem.2281 |
0.374 |
|
| 2015 |
Nguyen QL, Baire B, Hoye TR. Competition between classical and hexadehydro-Diels-Alder (HDDA) reactions of HDDA triynes with furan. Tetrahedron Letters. 56: 3265-3267. PMID 26028780 DOI: 10.1016/J.Tetlet.2014.12.053 |
0.708 |
|
| 2015 |
Pogula VD, Wang T, Hoye TR. Intramolecular [4 + 2] trapping of a hexadehydro-Diels-Alder (HDDA) benzyne by tethered arenes. Organic Letters. 17: 856-9. PMID 25671804 DOI: 10.1021/Ol5037024 |
0.793 |
|
| 2014 |
Woods BP, Hoye TR. Differential scanning calorimetry (DSC) as a tool for probing the reactivity of polyynes relevant to hexadehydro-Diels-Alder (HDDA) cascades. Organic Letters. 16: 6370-3. PMID 25470072 DOI: 10.1021/Ol503162K |
0.689 |
|
| 2014 |
Hoye TR, Baire B, Wang T. Tactics for Probing Aryne Reactivity: Mechanistic Studies of Silicon-oxygen Bond Cleavage During the Trapping of (HDDA-generated) Benzynes by Silyl Ethers. Chemical Science (Royal Society of Chemistry : 2010). 5: 545-550. PMID 25419449 DOI: 10.1039/C3Sc53014K |
0.712 |
|
| 2014 |
Willoughby PH, Niu D, Wang T, Haj MK, Cramer CJ, Hoye TR. Mechanism of the reactions of alcohols with o-benzynes. Journal of the American Chemical Society. 136: 13657-65. PMID 25232890 DOI: 10.1021/Ja502595M |
0.787 |
|
| 2014 |
Woods BP, Baire B, Hoye TR. Rates of hexadehydro-Diels-Alder (HDDA) cyclizations: impact of the linker structure. Organic Letters. 16: 4578-81. PMID 25153729 DOI: 10.1021/Ol502131R |
0.803 |
|
| 2014 |
Chen J, Baire B, Hoye TR. CYCLOADDITION REACTIONS OF AZIDE, FURAN, AND PYRROLE UNITS WITH BENZYNES GENERATED BY THE HEXADEHYDRO-DIELS-ALDER (HDDA) REACTION. Heterocycles. 88: 1191-1200. PMID 24910496 DOI: 10.3987/Com-13-S(S)83 |
0.721 |
|
| 2014 |
Hassig CA, Zeng FY, Kung P, Kiankarimi M, Kim S, Diaz PW, Zhai D, Welsh K, Morshedian S, Su Y, O'Keefe B, Newman DJ, Rusman Y, Kaur H, Salomon CE, ... ... Hoye TR, et al. Ultra-High-Throughput Screening of Natural Product Extracts to Identify Proapoptotic Inhibitors of Bcl-2 Family Proteins. Journal of Biomolecular Screening. 19: 1201-1211. PMID 24870016 DOI: 10.1177/1087057114536227 |
0.719 |
|
| 2014 |
Wohl AR, Michel AR, Kalscheuer S, Macosko CW, Panyam J, Hoye TR. Silicate esters of paclitaxel and docetaxel: synthesis, hydrophobicity, hydrolytic stability, cytotoxicity, and prodrug potential. Journal of Medicinal Chemistry. 57: 2368-79. PMID 24564494 DOI: 10.1021/Jm401708F |
0.697 |
|
| 2014 |
Willoughby PH, Jansma MJ, Hoye TR. A guide to small-molecule structure assignment through computation of (¹H and ¹³C) NMR chemical shifts. Nature Protocols. 9: 643-60. PMID 24556787 DOI: 10.1038/Nprot.2014.042 |
0.785 |
|
| 2014 |
Marell DJ, Emond SJ, Kulshrestha A, Hoye TR. Analysis of seven-membered lactones by computational NMR methods: proton NMR chemical shift data are more discriminating than carbon. The Journal of Organic Chemistry. 79: 752-8. PMID 24354614 DOI: 10.1021/Jo402627S |
0.769 |
|
| 2014 |
Niu D, Hoye TR. The aromatic ene reaction. Nature Chemistry. 6: 34-40. PMID 24345944 DOI: 10.1038/Nchem.1797 |
0.636 |
|
| 2014 |
Niu D, Wang T, Woods BP, Hoye TR. Dichlorination of (hexadehydro-Diels-Alder generated) benzynes and a protocol for interrogating the kinetic order of bimolecular aryne trapping reactions. Organic Letters. 16: 254-7. PMID 24329102 DOI: 10.1021/Ol403258C |
0.794 |
|
| 2014 |
Hoye TR, Chen J, Baire B. ChemInform Abstract: Cycloaddition Reactions of Azide, Furan, and Pyrrole Units with Benzynes Generated by the Hexadehydro-Diels-Alder (HDDA) Reaction. Cheminform. 45: no-no. DOI: 10.1002/chin.201423123 |
0.692 |
|
| 2013 |
Izgu EC, Hoye TR. Total synthesis of (±)-leuconolam: intramolecular allylic silane addition to a maleimide carbonyl group. Chemical Science (Royal Society of Chemistry : 2010). 4: 2262-2266. PMID 25419448 DOI: 10.1039/C3Sc00056G |
0.772 |
|
| 2013 |
Niu D, Willoughby PH, Woods BP, Baire B, Hoye TR. Alkane desaturation by concerted double hydrogen atom transfer to benzyne. Nature. 501: 531-4. PMID 24067712 DOI: 10.1038/Nature12492 |
0.808 |
|
| 2013 |
Pustulka KM, Wohl AR, Lee HS, Michel AR, Han J, Hoye TR, McCormick AV, Panyam J, Macosko CW. Flash nanoprecipitation: particle structure and stability. Molecular Pharmaceutics. 10: 4367-77. PMID 24053447 DOI: 10.1021/Mp400337F |
0.659 |
|
| 2013 |
Hoye TR, Ayyad SE, Beckord HJ, Brown SG. New diarylheptanoids and a hydroxylated ottelione from Ottelia alismoides. Natural Product Communications. 8: 351-8. PMID 23678810 DOI: 10.1177/1934578X1300800320 |
0.58 |
|
| 2013 |
Baire B, Niu D, Willoughby PH, Woods BP, Hoye TR. Synthesis of complex benzenoids via the intermediate generation of o-benzynes through the hexadehydro-Diels-Alder reaction. Nature Protocols. 8: 501-8. PMID 23411632 DOI: 10.1038/Nprot.2013.017 |
0.824 |
|
| 2013 |
Dings RP, Levine JI, Brown SG, Astorgues-Xerri L, MacDonald JR, Hoye TR, Raymond E, Mayo KH. Polycationic calixarene PTX013, a potent cytotoxic agent against tumors and drug resistant cancer. Investigational New Drugs. 31: 1142-50. PMID 23392775 DOI: 10.1007/S10637-013-9932-0 |
0.544 |
|
| 2012 |
Hoye TR, Baire B, Niu D, Willoughby PH, Woods BP. The hexadehydro-Diels-Alder reaction. Nature. 490: 208-12. PMID 23060191 DOI: 10.1038/Nature11518 |
0.821 |
|
| 2012 |
Izgu EC, Hoye TR. o-(Trialkylstannyl)anilines and Their Utility in Stille Cross-Coupling: Direct Introduction of the 2-Aminophenyl Substituent. Tetrahedron Letters. 53: 4938-4941. PMID 22984300 DOI: 10.1016/J.Tetlet.2012.06.138 |
0.762 |
|
| 2012 |
Jansma MJ, Hoye TR. Oxyanionic sigmatropic rearrangements relevant to cyclooctadienone formation in penostatins I and F. Organic Letters. 14: 4738-41. PMID 22963036 DOI: 10.1021/Ol3019488 |
0.79 |
|
| 2012 |
Han J, Zhu Z, Qian H, Wohl AR, Beaman CJ, Hoye TR, Macosko CW. A simple confined impingement jets mixer for flash nanoprecipitation. Journal of Pharmaceutical Sciences. 101: 4018-23. PMID 22777753 DOI: 10.1002/Jps.23259 |
0.654 |
|
| 2012 |
D'Addio SM, Saad W, Ansell SM, Squiers JJ, Adamson DH, Herrera-Alonso M, Wohl AR, Hoye TR, Macosko CW, Mayer LD, Vauthier C, Prud'homme RK. Effects of block copolymer properties on nanocarrier protection from in vivo clearance. Journal of Controlled Release : Official Journal of the Controlled Release Society. 162: 208-17. PMID 22732478 DOI: 10.1016/J.Jconrel.2012.06.020 |
0.66 |
|
| 2012 |
Brown SG, Jansma MJ, Hoye TR. Case study of empirical and computational chemical shift analyses: reassignment of the relative configuration of phomopsichalasin to that of diaporthichalasin. Journal of Natural Products. 75: 1326-31. PMID 22731865 DOI: 10.1021/Np300248W |
0.779 |
|
| 2012 |
Niu D, Hoye TR. A concise total synthesis of (±)- and (-)-okilactomycin D. Organic Letters. 14: 828-31. PMID 22273402 DOI: 10.1021/Ol203355G |
0.573 |
|
| 2012 |
Gurusamy-Thangavelu SA, Emond SJ, Kulshrestha A, Hillmyer MA, MacOsko CW, Tolman WB, Hoye TR. Polyurethanes based on renewable polyols from bioderived lactones Polymer Chemistry. 3: 2941-2948. DOI: 10.1039/C2Py20454A |
0.779 |
|
| 2011 |
Qian H, Wohl AR, Crow JT, Macosko CW, Hoye TR. A Strategy for Control of "Random" Copolymerization of Lactide and Glycolide: Application to Synthesis of PEG-b-PLGA Block Polymers Having Narrow Dispersity. Macromolecules. 44: 7132-7140. PMID 22287809 DOI: 10.1021/Ma201169Z |
0.695 |
|
| 2011 |
Hoye TR, Jeon J, Tennakoon MA. Allylmalonate as an activator subunit for the initiation of relay ring-closing metathesis reactions. Angewandte Chemie (International Ed. in English). 50: 2141-3. PMID 21344570 DOI: 10.1002/Anie.201005044 |
0.809 |
|
| 2011 |
Izgu EC, Burns AC, Hoye TR. Access to functionalized steroid side chains via modified Julia olefination. Organic Letters. 13: 703-5. PMID 21244047 DOI: 10.1021/Ol102936Z |
0.798 |
|
| 2011 |
Burns AC, Sorensen PW, Hoye TR. Synthesis and olfactory activity of unnatural, sulfated 5β-bile acid derivatives in the sea lamprey (Petromyzon marinus). Steroids. 76: 291-300. PMID 21145335 DOI: 10.1016/J.Steroids.2010.11.010 |
0.655 |
|
| 2010 |
May AE, Connell NT, Dahlmann HA, Hoye TR. A Useful Modification of the Evans Magnesium Halide-Catalyzed anti-Aldol Reaction: Application to Enolizable Aldehydes. Synlett : Accounts and Rapid Communications in Synthetic Organic Chemistry. 13: 1984-1986. PMID 26823643 DOI: 10.1055/S-0030-1258480 |
0.627 |
|
| 2010 |
Hoye TR, Danielson ME, May AE, Zhao H. Total synthesis of (-)-callipeltoside A. The Journal of Organic Chemistry. 75: 7052-60. PMID 20932014 DOI: 10.1021/Jo101598Y |
0.81 |
|
| 2010 |
May AE, Hoye TR. Room temperature acylketene formation? 1,3-Dioxin-4-ones via silver(I) activation of phenylthioacetoacetate in the presence of ketones. The Journal of Organic Chemistry. 75: 6054-6. PMID 20690691 DOI: 10.1021/Jo101372V |
0.569 |
|
| 2010 |
Hoye TR, Jeon J, Kopel LC, Ryba TD, Tennakoon MA, Wang Y. Total synthesis of peloruside A through kinetic lactonization and relay ring-closing metathesis cyclization reactions. Angewandte Chemie (International Ed. in English). 49: 6151-5. PMID 20645374 DOI: 10.1002/Anie.201002293 |
0.812 |
|
| 2010 |
Hoye TR, Erickson SE, Erickson-Birkedahl SL, Hale CR, Izgu EC, Mayer MJ, Notz PK, Renner MK. Long-range shielding effects in the (1)H NMR spectra of Mosher-like ester derivatives. Organic Letters. 12: 1768-71. PMID 20337423 DOI: 10.1021/Ol1003862 |
0.762 |
|
| 2010 |
Hoye TR, Jeffrey CS, Nelson DP. Dynamic kinetic resolution during a vinylogous Payne rearrangement: a concise synthesis of the polar pharmacophoric subunit of (+)-scyphostatin. Organic Letters. 12: 52-5. PMID 19968321 DOI: 10.1021/Ol902459Z |
0.762 |
|
| 2010 |
Hoye T, Jeon J, Kopel L, Ryba T, Tennakoon M, Wang Y. Synthesis of (+)-Peloruside A Synfacts. 2010: 1331-1331. DOI: 10.1055/S-0030-1258876 |
0.784 |
|
| 2010 |
May AE, Connell NT, Dahlmann HA, Hoye TR. A useful modification of the Evans magnesium halide catalyzed anti-aldol reaction: Application to enolizable aldehydes Synlett. 1984-1986. DOI: 10.1055/s-0030-1258480 |
0.578 |
|
| 2010 |
HOYE TR, SURIANO JA. ChemInform Abstract: (W(CO)5×THF)-Mediated Pauson-Khand Reaction: Cyclizations of 1,6- Enynes via a Batch-Catalytic Protocol. Cheminform. 24: no-no. DOI: 10.1002/chin.199322165 |
0.314 |
|
| 2010 |
Hoye TR, Jeon J. Metathesis Involving a Relay and Applications in Natural Product Synthesis Metathesis in Natural Product Synthesis: Strategies, Substrates and Catalysts. 261-285. DOI: 10.1002/9783527629626.ch9 |
0.474 |
|
| 2009 |
Ji S, Zhu Z, Hoye TR, Macosko CW. Maleimide Functionalized Poly(ε-caprolactone)-b-poly(ethylene glycol) (PCL-PEG-MAL): Synthesis, Nanoparticle Formation, and Thiol Conjugation. Macromolecular Chemistry and Physics. 210: 823. PMID 21731402 DOI: 10.1002/Macp.200900025 |
0.54 |
|
| 2009 |
Kobayashi S, Lu C, Hoye TR, Hillmyer MA. Controlled polymerization of a cyclic diene prepared from the ring-closing metathesis of a naturally occurring monoterpene. Journal of the American Chemical Society. 131: 7960-1. PMID 19456157 DOI: 10.1021/Ja9027567 |
0.321 |
|
| 2009 |
Efange SM, Brun R, Wittlin S, Connolly JD, Hoye TR, McAkam T, Makolo FL, Mbah JA, Nelson DP, Nyongbela KD, Wirmum CK. Okundoperoxide, a bicyclic cyclofarnesylsesquiterpene endoperoxide from Scleria striatinux with antiplasmodial activity. Journal of Natural Products. 72: 280-3. PMID 19199815 DOI: 10.1021/Np800338P |
0.548 |
|
| 2009 |
Levine JI, Dings RPM, Loren ML, Hoye TR, Mayo KH. Abstract A141: Synthesis and bioactivity of core‐expanded calixarene‐based antitumor agents Molecular Cancer Therapeutics. 8. DOI: 10.1158/1535-7163.Targ-09-A141 |
0.307 |
|
| 2008 |
Ji S, Hoye TR, Macosko CW. Diamino Telechelic Polybutadienes for Solventless Styrene-butadiene-styrene (SBS) Triblock Copolymer Formation. Polymer. 49: 5307-5313. PMID 19907636 DOI: 10.1016/J.Polymer.2008.09.026 |
0.584 |
|
| 2008 |
Hoye TR, Danielson ME, May AE, Zhao H. Dual macrolactonization/pyran-hemiketal formation via acylketenes: applications to the synthesis of (-)-callipeltoside A and a lyngbyaloside B model system. Angewandte Chemie (International Ed. in English). 47: 9743-6. PMID 18979468 DOI: 10.1002/Anie.200804049 |
0.779 |
|
| 2008 |
Gindy ME, Ji S, Hoye TR, Panagiotopoulos AZ, Prud'homme RK. Preparation of poly(ethylene glycol) protected nanoparticles with variable bioconjugate ligand density. Biomacromolecules. 9: 2705-11. PMID 18759476 DOI: 10.1021/Bm8002013 |
0.569 |
|
| 2008 |
Wiitala KW, Tian Z, Cramer CJ, Hoye TR. A thermal decarbonylation of penam beta-lactams. The Journal of Organic Chemistry. 73: 3024-31. PMID 18348573 DOI: 10.1021/Jo7023834 |
0.561 |
|
| 2008 |
May AE, Willoughby PH, Hoye TR. Decarboxylative isomerization of N-Acyl-2-oxazolidinones to 2-oxazolines. The Journal of Organic Chemistry. 73: 3292-4. PMID 18345687 DOI: 10.1021/Jo800076F |
0.799 |
|
| 2007 |
Hoye TR, Jeffrey CS, Shao F. Mosher ester analysis for the determination of absolute configuration of stereogenic (chiral) carbinol carbons. Nature Protocols. 2: 2451-8. PMID 17947986 DOI: 10.1038/Nprot.2007.354 |
0.744 |
|
| 2007 |
Zhu Z, Anacker JL, Ji S, Hoye TR, Macosko CW, Prud'homme RK. Formation of block copolymer-protected nanoparticles via reactive impingement mixing. Langmuir : the Acs Journal of Surfaces and Colloids. 23: 10499-504. PMID 17824626 DOI: 10.1021/La701420Z |
0.538 |
|
| 2007 |
Wiitala KW, Cramer CJ, Hoye TR. Comparison of various density functional methods for distinguishing stereoisomers based on computed (1)H or (13)C NMR chemical shifts using diastereomeric penam beta-lactams as a test set. Magnetic Resonance in Chemistry : Mrc. 45: 819-29. PMID 17729215 DOI: 10.1002/Mrc.2045 |
0.466 |
|
| 2007 |
Hoye TR, Dvornikovs V, Fine JM, Anderson KR, Jeffrey CS, Muddiman DC, Shao F, Sorensen PW, Wang J. Details of the structure determination of the sulfated steroids PSDS and PADS: new components of the sea lamprey (petromyzon marinus) migratory pheromone. The Journal of Organic Chemistry. 72: 7544-50. PMID 17718505 DOI: 10.1021/Jo070957L |
0.784 |
|
| 2007 |
Hoye T, Eklov B, Jeon J, Khoroosi M. Synthesis of (+)-Gigantecin Synfacts. 2007: 0009-0009. DOI: 10.1055/S-2006-955655 |
0.797 |
|
| 2007 |
Wiitala KW, Al-Rashid ZF, Dvornikovs V, Hoye TR, Cramer CJ. Evaluation of various DFT protocols for computing1H and 13C chemical shifts to distinguish stereoisomers: Diastereomeric 2-, 3-, and 4-methylcyclohexanols as a test set Journal of Physical Organic Chemistry. 20: 345-354. DOI: 10.1002/Poc.1151 |
0.788 |
|
| 2006 |
Wiitala KW, Hoye TR, Cramer CJ. Hybrid Density Functional Methods Empirically Optimized for the Computation of (13)C and (1)H Chemical Shifts in Chloroform Solution. Journal of Chemical Theory and Computation. 2: 1085-92. PMID 26633067 DOI: 10.1021/Ct6001016 |
0.455 |
|
| 2006 |
Chen X, Dings RP, Nesmelova I, Debbert S, Haseman JR, Maxwell J, Hoye TR, Mayo KH. Topomimetics of amphipathic beta-sheet and helix-forming bactericidal peptides neutralize lipopolysaccharide endotoxins. Journal of Medicinal Chemistry. 49: 7754-65. PMID 17181157 DOI: 10.1021/Jm0610447 |
0.759 |
|
| 2006 |
Hoye TR, Dvornikovs V, Sizova E. Silylative Dieckmann-like cyclizations of ester-imides (and diesters). Organic Letters. 8: 5191-4. PMID 17078675 DOI: 10.1021/Ol061988Q |
0.794 |
|
| 2006 |
Hoye TR, Eklov BM, Jeon J, Khoroosi M. Sequencing of three-component olefin metatheses: total synthesis of either (+)-gigantecin or (+)-14-deoxy-9-oxygigantecin. Organic Letters. 8: 3383-6. PMID 16836411 DOI: 10.1021/Ol061383U |
0.802 |
|
| 2006 |
Hoye TR, Dvornikovs V. Comparative Diels-Alder reactivities within a family of valence bond isomers: a biomimetic total synthesis of (+/-)-UCS1025A. Journal of the American Chemical Society. 128: 2550-1. PMID 16492035 DOI: 10.1021/Ja0581999 |
0.408 |
|
| 2006 |
Hoye TR, Kopel LC, Ryba TD. In situ generation and nucleophilic capture of 1,n-dial equivalents from 1,n-dioates (α,ω-diesters) Synthesis. 1572-1574. DOI: 10.1055/S-2006-926465 |
0.797 |
|
| 2006 |
Hoye TR, Renner MK. Erratum: MTPA (Mosher) amides of cyclic secondary amines: Conformational aspects and a useful method for assignment of amine configuration (Journal of Organic Chemistry (1996) 61 (2062-2063)) Journal of Organic Chemistry. 71. DOI: 10.1021/Jo063306I |
0.319 |
|
| 2006 |
Hoye TR, Jeffrey CS. Student empowerment through "mini-microscale" reactions: The expoxidation of 1 mg of geraniol Journal of Chemical Education. 83: 919-920. DOI: 10.1021/Ed083P919 |
0.681 |
|
| 2006 |
Wiitala KW, Hoye TR, Cramer CJ. Hybrid density functional methods empirically optimized for the computation of 13C and 1H chemical shifts in chloroform solution Journal of Chemical Theory and Computation. 2: 1085-1092. DOI: 10.1021/ct6001016 |
0.376 |
|
| 2005 |
Sorensen PW, Fine JM, Dvornikovs V, Jeffrey CS, Shao F, Wang J, Vrieze LA, Anderson KR, Hoye TR. Mixture of new sulfated steroids functions as a migratory pheromone in the sea lamprey. Nature Chemical Biology. 1: 324-8. PMID 16408070 DOI: 10.1038/Nchembio739 |
0.781 |
|
| 2005 |
Hoye TR, Ryba TD. Divergent kinetic control of classical versus ozonolytic lactonization: mechanism-based diastereoselection. Journal of the American Chemical Society. 127: 8256-7. PMID 15941238 DOI: 10.1021/Ja051604B |
0.684 |
|
| 2005 |
Hoye TR, Aspaas AW, Eklov BM, Ryba TD. Reaction titration: a convenient method for titering reactive hydride agents (Red-Al, LiAlH4, DIBALH, L-Selectride, NaH, and KH) by No-D NMR spectroscopy. Organic Letters. 7: 2205-8. PMID 15901170 DOI: 10.1021/Ol0506011 |
0.787 |
|
| 2005 |
Hoye TR, Wang J. Alkyne haloallylation [with Pd(II)] as a core strategy for macrocycle synthesis: a total synthesis of (-)-haterumalide NA/(-)-oocydin A. Journal of the American Chemical Society. 127: 6950-1. PMID 15884928 DOI: 10.1021/Ja051749I |
0.722 |
|
| 2005 |
Hoye TR, Kabrhel JE, Hoye RC. No-D NMR study of the pathway for n-BuLi "oxidation" of 1,5-cyclooctadiene to dilithium cyclooctatetraene dianion [Li2COT2-]. Organic Letters. 7: 275-7. PMID 15646976 DOI: 10.1021/Ol0477024 |
0.787 |
|
| 2005 |
Hoye T, Wang J. Synthesis of (-)-Haterumalide NA Synfacts. 2005: 195-195. DOI: 10.1055/S-2005-916053 |
0.648 |
|
| 2005 |
Ji S, Hoye TR, Macosko CW. Primary amine (-NH 2) quantification in polymers: Functionality by 19F NMR spectroscopy Macromolecules. 38: 4679-4686. DOI: 10.1021/Ma050178B |
0.543 |
|
| 2005 |
Macosko CW, Jeon HK, Hoye TR. Reactions at polymer-polymer interfaces for blend compatibilization Progress in Polymer Science (Oxford). 30: 939-947. DOI: 10.1016/J.Progpolymsci.2005.06.003 |
0.322 |
|
| 2004 |
Hoye TR, Jeffrey CS, Tennakoon MA, Wang J, Zhao H. Relay ring-closing metathesis (RRCM): a strategy for directing metal movement throughout olefin metathesis sequences. Journal of the American Chemical Society. 126: 10210-1. PMID 15315410 DOI: 10.1021/Ja046385T |
0.783 |
|
| 2004 |
Hoye TR, Eklov BM, Voloshin M. No-D NMR spectroscopy as a convenient method for titering organolithium (RLi), RMgX, and LDA solutions. Organic Letters. 6: 2567-70. PMID 15255692 DOI: 10.1021/Ol049145R |
0.79 |
|
| 2004 |
Hoye TR, Eklov BM, Ryba TD, Voloshin M, Yao LJ. No-D NMR (no-deuterium proton NMR) spectroscopy: a simple yet powerful method for analyzing reaction and reagent solutions. Organic Letters. 6: 953-6. PMID 15012073 DOI: 10.1021/Ol049979+ |
0.804 |
|
| 2004 |
Ji S, Hoye TR, Macosko CW. Controlled synthesis of high molecular weight telechelic polybutadienes by ring-opening metathesis polymerization Macromolecules. 37: 5485-5489. DOI: 10.1021/Ma0493067 |
0.556 |
|
| 2004 |
Jeon HK, Macosko CW, Moon B, Hoye TR, Yin Z. Coupling Reactions of End- vs Mid-Functional Polymers Macromolecules. 37: 2563-2571. DOI: 10.1021/Ma030581N |
0.557 |
|
| 2004 |
Jones TD, Macosko CW, Moon B, Hoye TR. Synthesis and reactive blending of amine and anhydride end-functional polyolefins Polymer. 45: 4189-4201. DOI: 10.1016/J.Polymer.2004.04.015 |
0.559 |
|
| 2003 |
Hoye TR, Hu M. Macrolactonization via Ti(IV)-mediated epoxy-acid coupling: a total synthesis of (-)-dactylolide [and zampanolide]. Journal of the American Chemical Society. 125: 9576-7. PMID 12904009 DOI: 10.1021/Ja035579Q |
0.532 |
|
| 2002 |
Hoye TR, Ayyad SE, Eklov BM, Hashish NE, Shier WT, El-Sayed KA, Hamann MT. Toward computing relative configurations: 16-epi-latrunculin B, a new stereoisomer of the actin polymerization inhibitor latrunculin B. Journal of the American Chemical Society. 124: 7405-10. PMID 12071749 DOI: 10.1021/Ja025734L |
0.795 |
|
| 2002 |
Hoye TR, Zhao H. A method for easily determining coupling constant values: an addendum to "A practical guide to first-order multiplet analysis in 1H NMR spectroscopy". The Journal of Organic Chemistry. 67: 4014-6. PMID 12054933 DOI: 10.1021/Jo001139V |
0.444 |
|
| 2002 |
Moon B, Hoye TR, Macosko CW. Synthesis and application of fluorescently labeled phthalic anhydride (PA) functionalized polymers by ATRP Polymer. 43: 5501-5509. DOI: 10.1016/S0032-3861(02)00406-8 |
0.545 |
|
| 2002 |
Lu QW, Hoye TR, Macosko CW. Reactivity of common functional groups with urethanes: Models for reactive compatibilization of thermoplastic polyurethane blends Journal of Polymer Science, Part a: Polymer Chemistry. 40: 2310-2328. DOI: 10.1002/Pola.10310 |
0.399 |
|
| 2001 |
Hoye TR, Van Veidhuizen JJ, Vos TJ, Zhao P. A useful modification of the Kraus procedure1 for preparation of ω-bromo-1-alkenes by HMPA-promoted elimination of HBR from 1,ω-dibromoalkanes Synthetic Communications. 31: 1367-1371. DOI: 10.1081/Scc-100104046 |
0.304 |
|
| 2001 |
Moon B, Hoye TR, Macosko CW. Synthesis of end- and mid-phthalic anhydride functional polymers by atom transfer radical polymerization Macromolecules. 34: 7941-7951. DOI: 10.1021/Ma010475Q |
0.579 |
|
| 2000 |
Hoye TR, Tennakoon MA. Synthesis (and alternative proof of configuration) of the scyphostatin C(1')-C(20') trienoyl fragment. Organic Letters. 2: 1481-3. PMID 10814478 |
0.819 |
|
| 2000 |
Hoye TR, Humpai PE, Moon B. Total synthesis of (-)-cylindrocyclophane a via a double Horner-Emmons macrocyclic dimerization event [2] Journal of the American Chemical Society. 122: 4982-4983. DOI: 10.1021/Ja000429Q |
0.552 |
|
| 2000 |
Hoye TR, Hamad ASS, Koltun DO, Tennakoon MA. An NMR method for determination of configuration of β-substituted carboxylic acids Tetrahedron Letters. 41: 2289-2293. DOI: 10.1016/S0040-4039(00)00163-5 |
0.783 |
|
| 2000 |
Moon B, Hoye TR, Macosko CW. Anionic synthesis and detection of fluorescence-labeled polymers with a terminal anhydride group Journal of Polymer Science, Part a: Polymer Chemistry. 38: 2177-2185. DOI: 10.1002/(Sici)1099-0518(20000615)38:12<2177::Aid-Pola60>3.0.Co;2-5 |
0.54 |
|
| 1999 |
Hoye TR, Zhao H. Some allylic substituent effects in ring-closing metathesis reactions: allylic alcohol activation. Organic Letters. 1: 1123-5. PMID 10825965 |
0.313 |
|
| 1999 |
Hoye TR, Donaldson SM, Vos TJ. An enyne metathesis/(4 + 2)-dimerization route to (+/-)-differolide. Organic Letters. 1: 277-9. PMID 10822563 DOI: 10.1021/Ol9905912 |
0.416 |
|
| 1999 |
Hoye TR, Zhao H. Synthesis of a C(1)-C(14)-containing fragment of callipeltoside A. Organic Letters. 1: 169-71. PMID 10822555 DOI: 10.1021/Ol9906514 |
0.557 |
|
| 1999 |
Hoye TR, Chen M, Hoang B, Mi L, Priest OP. Total synthesis of michellamines A-C, korupensamines A-D, and ancistrobrevine B Journal of Organic Chemistry. 64: 7184-7201. DOI: 10.1021/Jo9908187 |
0.831 |
|
| 1999 |
Hoye TR, Promo MA. Silicon tethered ring-closing metathesis reactions for self- and cross- coupling of alkenols Tetrahedron Letters. 40: 1429-1432. DOI: 10.1016/S0040-4039(98)02697-5 |
0.39 |
|
| 1998 |
Cernohous JJ, Macosko CW, Hoye TR. Amine-terminal polystyrenes: A new strategy for synthesis and new methods for determination of functionality Macromolecules. 31: 3759-3763. DOI: 10.1021/Ma971142P |
0.373 |
|
| 1998 |
Brown DG, Hoye TR, Brisbois RG. Synthesis of Azulenone Skeletons by Reaction of 2-Phenyl-2-acylketenes [RCO(Ph)C=C=O] with Alkynyl Ethers: Mechanistic Aspects and Further Transformations Journal of Organic Chemistry. 63: 1630-1636. DOI: 10.1021/Jo9719315 |
0.459 |
|
| 1998 |
Goodwin TE, Cousins DM, Debenham SD, Green JL, Guyer ML, Jacobs EG, Hoye TR, Koltun DO, Vyvyan JR. Synthesis of Conformationally Mobile Bicyclic Tetrahydro-1,2-oxazines by Isomerization of Isoxazolidinylmethyl Tosylates Journal of Organic Chemistry. 63: 4485-4488. DOI: 10.1021/Jo971299F |
0.706 |
|
| 1998 |
Hoye TR, Koltun DO. An NMR strategy for determination of configuration of remote stereogenic centers: 3-methylcarboxylic acids Journal of the American Chemical Society. 120: 4638-4643. DOI: 10.1021/Ja972664N |
0.341 |
|
| 1998 |
Hoye TR, Cernohous JJ, Pfister KP. An efficient (one-pot) synthesis of a new class of cyclophanes Tetrahedron Letters. 39: 1857-1860. DOI: 10.1016/S0040-4039(98)00119-1 |
0.385 |
|
| 1997 |
Hoye TR, Mi L. A Convenient Synthesis of 1-Bromo- 4,5-dimethoxy-7-methylnaphthalene, a Naphthol Derivative Useful for Construction of Naphthylisoquinoline Alkaloids. The Journal of Organic Chemistry. 62: 8586-8588. PMID 11672012 DOI: 10.1021/Jo9713262 |
0.356 |
|
| 1997 |
Cernohous JJ, Macosko CW, Hoye TR. Anionic synthesis of polymers functionalized with a terminal anhydride group Macromolecules. 30: 5213-5219. DOI: 10.1021/Ma9702096 |
0.362 |
|
| 1996 |
Hoye TR, Chen M. Studies of Palladium-Catalyzed Cross-Coupling Reactions for Preparation of Highly Hindered Biaryls Relevant to the Korupensamine/Michellamine Problem. The Journal of Organic Chemistry. 61: 7940-7942. PMID 11667757 DOI: 10.1021/Jo960882D |
0.379 |
|
| 1996 |
Guégan P, Cernohous JJ, Khandpur AK, Hoye TR, Macosko CW. Anionic synthesis, modification, and characterization of ABC triblock copolymers Macromolecules. 29: 4605-4612. DOI: 10.1021/Ma951193R |
0.305 |
|
| 1996 |
Hoye TR, Renner MK. Applications of MTPA (Mosher) amides of secondary amines: Assignment of absolute configuration in chiral cyclic amines Journal of Organic Chemistry. 61: 8489-8495. DOI: 10.1021/Jo960373B |
0.369 |
|
| 1996 |
Hoye TR, Renner MK. MTPA (Mosher) amides of cyclic secondary amines: Conformational aspects and a useful method for assignment of amine configuration Journal of Organic Chemistry. 61: 2056-2064. DOI: 10.1021/Jo952043H |
0.39 |
|
| 1996 |
Brown DG, Velthuisen EJ, Commerford JR, Brisbois RG, Hoye TR. A convenient synthesis of dimethyl (diazomethyl)phosphonate (Seyferth/Gilbert reagent) Journal of Organic Chemistry. 61: 2540-2541. DOI: 10.1021/Jo951944N |
0.405 |
|
| 1996 |
Hoye TR, Ye Z, Yao LJ, North JT. 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 Journal of the American Chemical Society. 118: 12074-12081. DOI: 10.1021/Ja962671W |
0.373 |
|
| 1996 |
Hoye TR, Ye Z. Highly efficient synthesis of the potent antitumor annonaceous acetogenin (+)-parviflorin Journal of the American Chemical Society. 118: 1801-1802. DOI: 10.1021/Ja953781Q |
0.373 |
|
| 1996 |
Hoye TR, Liang M. Total syntheses of korupensamine C and ancistrobrevine B Tetrahedron Letters. 37: 3097-3098. DOI: 10.1016/0040-4039(96)00525-4 |
0.324 |
|
| 1996 |
Hoye TR, Chen M. Total synthesis of (ent)-korupensamine D Tetrahedron Letters. 37: 3099-3100. DOI: 10.1016/0040-4039(96)00524-2 |
0.392 |
|
| 1996 |
Gassman PG, Tan L, Hoye TR. Intramolecular cationic cyclizations initiated by electrocyclic cleavage of cyclopropanes. Synthesis of trienic cyclopentane derivatives Tetrahedron Letters. 37: 439-442. DOI: 10.1016/0040-4039(95)02213-9 |
0.406 |
|
| 1995 |
Hoye TR, Vyvyan JR. Polycyclic cyclopropanes from reactions of alkene-containing Fischer carbene complexes and alkynes: A formal synthesis of (±)-carabrone Journal of Organic Chemistry. 60: 4184-4195. DOI: 10.1021/Jo00118A040 |
0.726 |
|
| 1995 |
Ramirez EA, Hoye TR. Determination of relative and absolute configuration in the annonaceous acetogenins Studies in Natural Products Chemistry. 17: 251-282. DOI: 10.1016/S1572-5995(05)80087-0 |
0.328 |
|
| 1995 |
Hoye TR, Tan L. Total synthesis of the potent antitumor, bis-tetrahydrofuranyl annonaceous acetogenins (+)-asimicin and (+)-bullatacin Tetrahedron Letters. 36: 1981-1984. DOI: 10.1016/0040-4039(95)00207-S |
0.39 |
|
| 1995 |
Brestensky DM, Hoye TR, Macosko CW. Tandem GC/MS: A useful tool for studying end-capping reactions of oligo(styryl)lithium anions Journal of Polymer Science Part a: Polymer Chemistry. 33: 1957-1967. DOI: 10.1002/Pola.1995.080331202 |
0.335 |
|
| 1994 |
Söderberg BC, York DC, Hoye TR, Rehberg GM, Suriano JA. Lithium and tetramethylammonium pentacarbonyl(1-oxidoethylidene)chromate(0) ↔ acetylpentacarbonylchromate(0) as acetyl anion equivalents for conjugate addition reactions with electron deficient alkenes Organometallics. 13: 4501-4509. DOI: 10.1021/Om00023A061 |
0.375 |
|
| 1994 |
Hoye TR, Hanson PR, Vyvyan JR. A practical guide to first-order multiplet analysis in 1H NMR spectroscopy Journal of Organic Chemistry. 59: 4096-4103. DOI: 10.1021/Jo00094A018 |
0.74 |
|
| 1994 |
Hoye TR, Crawford KB. Enolate and other carbon nucleophile alkylation reactions using 1,2-cyclic sulfates as terminal epoxide equivalents Journal of Organic Chemistry. 59: 520-522. DOI: 10.1021/Jo00082A005 |
0.35 |
|
| 1994 |
Hoye TR, Chen M, Mi L, Priest OP. Total synthesis of Michellamines A-C: Important anti-HIV agents Tetrahedron Letters. 35: 8747-8750. DOI: 10.1016/S0040-4039(00)78487-5 |
0.794 |
|
| 1994 |
Hoye TR, Hanson PR, Hasenwinkel LE, Ramirez EA, Zhuang Z. 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)] Tetrahedron Letters. 35: 8529-8532. DOI: 10.1016/S0040-4039(00)78428-0 |
0.531 |
|
| 1994 |
Hoye TR, Hanson PR, Hasenwinkel LE, Ramirez EA, Zhuang Z. Stereostructural studies on the 4-hydroxylated annonaceous acetogenins: Synthesis of model butenolides of known relative and absolute configuration involving an intriguing translactonization reaction Tetrahedron Letters. 35: 8525-8528. DOI: 10.1016/S0040-4039(00)78427-9 |
0.618 |
|
| 1994 |
Hoye TR, Humpal PE, Jiménez JI, Mayer MJ, Tan L, Ye Z. An efficient and versatile synthesis of the butenolide subunit of 4-hydroxylated annonaceous acetogenins Tetrahedron Letters. 35: 7517-7520. DOI: 10.1016/S0040-4039(00)78332-8 |
0.359 |
|
| 1993 |
Hoye TR, Chen K, Vyvyan JR. Preparation of Fischer carbene complexes by alkylation of acylmetalates with alkyl iodides Organometallics. 12: 2806-2809. DOI: 10.1021/Om00031A056 |
0.7 |
|
| 1993 |
Hoye TR, Suriano JA. Dicobaltoctacarbonyl-mediated cyclizations of electron-deficient alkynones Journal of Organic Chemistry. 58: 1659-1660. DOI: 10.1021/Jo00059A009 |
0.393 |
|
| 1993 |
Hoye TR, Suriano JA. A [W(CO)5·THF]-mediated pauson-khand reaction cyclizations of 1,6-enynes via a batch-catalytic protocol Journal of the American Chemical Society. 115: 1154-1156. DOI: 10.1021/Ja00056A053 |
0.419 |
|
| 1993 |
Hoye TR, Hanson PR. Synthesis of (-)-bullatacin: The enantiomer of a potent, antitumor, 4-hydroxylated, Annonaceous acetogenin Tetrahedron Letters. 34: 5043-5046. DOI: 10.1016/S0040-4039(00)60671-8 |
0.582 |
|
| 1992 |
Hoye TR, Suriano JA. Reactions of pentacarbonyl(1-methoxyethylidene)molybdenum and -tungsten with α,ω-enynes: Comparison with the chromium analogue and resulting mechanistic ramifications Organometallics. 11: 2044-2050. DOI: 10.1021/Om00042A019 |
0.371 |
|
| 1992 |
Rieser MJ, Hui YH, Rupprecht JK, Kozlowski JF, Wood KV, McLaughlin JL, Hanson PR, Zhuang Z, Hoye TR. Determination of absolute configuration of stereogenic carbinol centers in annonaceous acetogenins by1H- and19F-NMR analysis of mosher ester derivatives Journal of the American Chemical Society. 114: 10203-10213. DOI: 10.1021/Ja00052A018 |
0.541 |
|
| 1992 |
Hoye TR, Dinsmore CJ. Tandem alkyne insertion and allyl sulfonium ylide rearrangement of γ,δ-alkynyl-α′-diazoketones Tetrahedron Letters. 33: 169-172. DOI: 10.1016/0040-4039(92)88041-3 |
0.676 |
|
| 1991 |
Hoye TR, Hanson PR. Assigning the relative stereochemistry between C(2) and C(4) of the 2-acetonyl-4-alkylbutyrolactone substructures of the appropriate annonaceous acetogenins Journal of Organic Chemistry. 56: 5092-5095. DOI: 10.1021/Jo00017A018 |
0.492 |
|
| 1991 |
Hoye TR, Hanson PR, Kovelesky AC, Ocain TD, Zhuang Z. Synthesis of (+)-(15,16,19,20,23,24)-hexepi-uvaricin: A bis(tetrahydrofuranyl) annonaceous acetogenin analogue Journal of the American Chemical Society. 113: 9369-9371. DOI: 10.1021/Ja00024A053 |
0.58 |
|
| 1991 |
Hoye TR, Dinsmore CJ. Rhodium(II) acetate catalyzed alkyne insertion reactions of .alpha.-diazo ketones: mechanistic inferences Journal of the American Chemical Society. 113: 4343-4345. DOI: 10.1021/Ja00011A055 |
0.672 |
|
| 1991 |
Hoye TR, Dinsmore CJ. Double (internal/external) alkyne insertion reactions of α-diazoketones Tetrahedron Letters. 32: 3755-3758. DOI: 10.1016/S0040-4039(00)79368-3 |
0.707 |
|
| 1990 |
Hoye TR, Rehberg GM. Manganese Fischer carbene chemistry: Reactions of Cp′(CO)2Mn=C(OMe/OLI)R with enynes, 1-hexyne, and acrylates Organometallics. 9: 3014-3015. DOI: 10.1021/Om00162A005 |
0.398 |
|
| 1990 |
Hoye TR, Dinsmore CJ, Johnson DS, Korkowski PF. Alkyne insertion reactions of metal-carbenes derived from enynyl-.alpha.-diazoketones [R'CN2COCR2CH2C.tplbond.C(CH2)n-2CH:CH2] Journal of Organic Chemistry. 55: 4518-4520. DOI: 10.1021/Jo00302A010 |
0.608 |
|
| 1990 |
Hoye TR, Rehberg GM. (1-Oxidoalkylidene)pentacarbonylchromium anion [R(O-)C:Cr(CO)5] .tautm. acylpentacarbonylchromate [acyl-Cr-(CO)5] chemistry: in situ preparation and reactions with alkynes and enynes Journal of the American Chemical Society. 112: 2841-2842. DOI: 10.1021/Ja00163A077 |
0.317 |
|
| 1990 |
Hoye TR, North JT. Thermodynamic control of stereochemistry in the synthesis of 1-oxaquinolizidine skeletal portions of xestospongin A Tetrahedron Letters. 31: 4281-4284. DOI: 10.1016/S0040-4039(00)97601-9 |
0.304 |
|
| 1989 |
Hoye TR, Rehberg GM. Reactions of (CO)5Cr=C(Me)N(CH2CH2)2 with enynes: Mechanistic insight and synthetic value of changing a carbene donor group from alkoxy to dialkylamino Organometallics. 8: 2070-2071. DOI: 10.1021/Om00110A042 |
0.404 |
|
| 1988 |
Hoye TR, Zhuang ZP. Validation of the 1H NMR chemical shift method for determination of stereochemistry in the bis(tetrahydrofuranyl) moiety of uvaricin-related acetogenins from annonaceae: Rolliniastatin 1 (and asimicin) Journal of Organic Chemistry. 53: 5578-5580. DOI: 10.1021/Jo00258A045 |
0.302 |
|
| 1988 |
Korkowski PF, Hoye TR, Rydberg DB. Fischer carbene mediated conversions of enynes to bi- and tricyclic cyclopropane-containing carbon skeletons Journal of the American Chemical Society. 110: 2676-2678. DOI: 10.1021/Ja00216A066 |
0.344 |
|
| 1987 |
Hoye TR, Peterson BH, Miller JD. Preparation of 5-alkyl-2-tert-butyl-1,3-dioxolan-4-ones by trimethylsilyl triflate catalyzed reactions between bis(trimethylsilyl) derivatives of α-hydroxy carboxylic acids and pivaldehyde Journal of Organic Chemistry. 52: 1351-1353. DOI: 10.1021/Jo00383A037 |
0.422 |
|
| 1987 |
Hoye TR, Jenkins SA. Asymmetric synthesis of achiral molecules: Meso selectivity Journal of the American Chemical Society. 109: 6196-6198. DOI: 10.1021/Ja00254A056 |
0.797 |
|
| 1986 |
Hoye TR, Suhadolnik JC. Stereocontrolled synthesis of 2,5-linked bistetrahydrofurans via the triepoxide cascade reaction Tetrahedron. 42: 2855-2862. DOI: 10.1016/S0040-4020(01)90574-5 |
0.434 |
|
| 1985 |
Hoye TR, Suhadolnik JC. 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 Journal of the American Chemical Society. 107: 5312-5313. DOI: 10.1021/Ja00304A068 |
0.354 |
|
| 1985 |
Hoye TR, Duff SR, King RS. Amidoacetone enolate anions: alkylation and Michael reaction Tetrahedron Letters. 26: 3433-3436. DOI: 10.1016/S0040-4039(00)98657-X |
0.413 |
|
| 1984 |
Borch RF, Hoye TR, Swanson TA. In situ preparation and fate of cis-4-hydroxycyclophosphamide and aldophosphamide: 1H and 31P NMR evidence for equilibration of cis- and trans-4-hydroxycyclophosphamide with aldophosphamide and its hydrate in aqueous solution. Journal of Medicinal Chemistry. 27: 490-4. PMID 6708051 DOI: 10.1021/Jm00370A010 |
0.401 |
|
| 1984 |
Hoye TR, Magee AS, Rosen RE. Stereochemistry of ethyl 2,6-dimethyl-4-oxocyclohex-2-enecarboxylate (6-methyl Hagemann's ester) and its products of conjugate addition by vinylmagnesium bromide/copper(I) iodide Journal of Organic Chemistry. 49: 3224-3226. DOI: 10.1002/Chin.198506145 |
0.309 |
|
| 1983 |
Hoye T, Caruso A, Dellaria, Jr. J, Kurth M. Additions and Corrections - Two Syntheses of d,l-Aplysistatin Journal of the American Chemical Society. 105: 6531-6531. DOI: 10.1021/Ja00359A602 |
0.452 |
|
| 1983 |
Hoye TR, Kurth MJ. Preparation of d,l-megaphone intermediates Tetrahedron Letters. 24: 4769-4772. DOI: 10.1016/S0040-4039(00)94003-6 |
0.505 |
|
| 1982 |
Hoye TR, Kaese PA. 3,4,5-Trimethoxyphenyllithium Synthetic Communications. 12: 49-52. DOI: 10.1080/00397918208080065 |
0.376 |
|
| 1982 |
Hoye TR, Magee AS, Trumper WS. 3,5-Hexadienoic esters: A convenient preparation Synthetic Communications. 12: 183-187. DOI: 10.1080/00397918208063675 |
0.384 |
|
| 1982 |
Hoye TR, Martin SJ, Peck DR. Intramolecular photochemical cycloaddition reactions of 3-(1,5-dimethylhex-4-enyl)cyclohex-2-enone: Regio- and stereochemical aspects Journal of Organic Chemistry. 47: 331-337. DOI: 10.1021/Jo00341A030 |
0.445 |
|
| 1982 |
Hoye TR, Caruso AJ, Magee AS. Preparation and Diels-Alder reactions of 1,1-dicarbonylalkenes Journal of Organic Chemistry. 47: 4152-4156. DOI: 10.1021/Jo00142A028 |
0.425 |
|
| 1981 |
Hoye TR, Caruso AJ. Total synthesis of dl-ancistrofuran: A study of cyclic ether formation Journal of Organic Chemistry. 46: 1198-1205. DOI: 10.1021/Jo00319A031 |
0.386 |
|
| 1981 |
Hoye TR. Steric impedence in the 1,3-photocycloaddition reaction between cyclopentene and anisole derivatives Tetrahedron Letters. 22: 2523-2526. DOI: 10.1016/S0040-4039(01)90509-X |
0.456 |
|
| 1981 |
Hoye TR, Kurth MJ, Lo V. Triphenylcarbenium and tris(P-bromophenyl)ammoniumyl ion induced lactonizations of (ω-benzyloxy and ω-P-methoxybenzyloxy methyl esters Tetrahedron Letters. 22: 815-818. DOI: 10.1016/0040-4039(81)80004-4 |
0.528 |
|
| 1981 |
Hoye TR, Caruso AJ, Kurth MJ. Internal nucleophilic termination in mercuric ion initiated diene cyclizations Journal of Organic Chemistry. 46: 3550-3552. DOI: 10.1002/Chin.198202219 |
0.482 |
|
| 1981 |
Hoye TR, Peck DR, Trumper PK. Symmetry in synthesis. Preparation and methylation of spiro dilactones Journal of the American Chemical Society. 103: 5618-5620. DOI: 10.1002/Chin.198150122 |
0.32 |
|
| 1980 |
Hoye TR, Bottorff KJ, Caruso AJ, Dellaria JF. Regio- and stereoselectivity in the ene reaction of N-phenyl-1,2,4-triazoline-3,5-dione with .alpha.,.beta.-unsaturated carbonyl substrates Journal of Organic Chemistry. 12: 4287-4292. DOI: 10.1021/Jo01310A007 |
0.328 |
|
| 1979 |
Hoye TR, Rother MJ. Mercuric acetate oxidation of 1-vinylcycloalkenes: Diels-Alder reactivity of resultant allylic diene acetates Journal of Organic Chemistry. 44: 458-461. DOI: 10.1021/Jo01317A037 |
0.318 |
|
| 1979 |
Hoye TR, Kurth MJ. Total synthesis of dl-aplysistatin Journal of the American Chemical Society. 101: 5065-5067. DOI: 10.1021/Ja00511A047 |
0.526 |
|
| 1979 |
Hoye TR, Kurth MJ. Mercuric trifluoroacetate mediated brominative cyclizations of dienes. Total synthesis of dl-3β-bromo-8-epicaparrapi oxide Journal of Organic Chemistry. 44: 3461-3467. DOI: 10.1002/Chin.198006263 |
0.311 |
|
| 1979 |
HOYE TR, KURTH MJ. ChemInform Abstract: TOTAL SYNTHESIS OF DL-APLYSISTATIN Chemischer Informationsdienst. 10. DOI: 10.1002/Chin.197948330 |
0.535 |
|
| 1978 |
Hoye TR, Kurth MJ. Brominative cyclizations of geranyl derivatives Journal of Organic Chemistry. 43: 3693-3697. DOI: 10.1021/Jo00413A012 |
0.367 |
|
| 1978 |
Hoye TR, Caruso AJ. A 1,3-diene-2-carboxylic ester synthesis; Reaction of alkylidene-γ-lactones with potassium and sodium phenyl selenoate Tetrahedron Letters. 19: 4611-4614. DOI: 10.1016/S0040-4039(01)85684-7 |
0.464 |
|
| 1973 |
HEINE HW, HOYE TR, WILLIARD PG, HOYE RC. ChemInform Abstract: DIAZIRIDINES PART 2, THE ADDITION OF DIAZIRIDINES TO ELECTROPHILIC ACETYLENES Chemischer Informationsdienst. 4: no-no. DOI: 10.1002/Chin.197348233 |
0.676 |
|
| 1973 |
HEINE HW, WILLIARD PG, HOYE TR. ChemInform Abstract: SYNTH. UND RK. EINIGER 1-NITROARYL-DIAZIRIDINE Chemischer Informationsdienst. 4: no-no. DOI: 10.1002/Chin.197302230 |
0.681 |
|
| 1972 |
Heine HW, Williard PG, Hoye TR. Synthesis and reactions of some 1-(nitroaryl)diaziridines Journal of Organic Chemistry. 37: 2980-2983. DOI: 10.1021/Jo00984A014 |
0.765 |
|
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