Mosher ester analysis for the determination of absolute configuration of stereogenic (chiral) carbinol carbons TR Hoye, CS Jeffrey, F Shao Nature protocols 2 (10), 2451-2458, 2007 | 887 | 2007 |
The hexadehydro-Diels–Alder reaction TR Hoye, B Baire, D Niu, PH Willoughby, BP Woods Nature 490 (7419), 208-212, 2012 | 407 | 2012 |
A guide to small-molecule structure assignment through computation of (1H and 13C) NMR chemical shifts PH Willoughby, MJ Jansma, TR Hoye Nature protocols 9 (3), 643-660, 2014 | 370 | 2014 |
A continuous catalytic system for biodiesel production CV McNeff, LC McNeff, B Yan, DT Nowlan, M Rasmussen, AE Gyberg, ... Applied Catalysis A: General 343 (1-2), 39-48, 2008 | 304 | 2008 |
Determination of absolute configuration of stereogenic carbinol centers in annonaceous acetogenins by proton and fluorine 19-NMR analysis of Mosher ester derivatives MJ Rieser, YH Hui, JK Rupprecht, JF Kozlowski, KV Wood, JL McLaughlin, ... Journal of the American Chemical Society 114 (26), 10203-10213, 1992 | 304 | 1992 |
Relay ring-closing metathesis (RRCM): A strategy for directing metal movement throughout olefin metathesis sequences TR Hoye, CS Jeffrey, MA Tennakoon, J Wang, H Zhao Journal of the American Chemical Society 126 (33), 10210-10211, 2004 | 288 | 2004 |
Mixture of new sulfated steroids functions as a migratory pheromone in the sea lamprey PW Sorensen, JM Fine, V Dvornikovs, CS Jeffrey, F Shao, J Wang, ... Nature Chemical Biology 1 (6), 324-328, 2005 | 279 | 2005 |
Some allylic substituent effects in ring-closing metathesis reactions: Allylic alcohol activation TR Hoye, H Zhao Organic letters 1 (7), 1123-1125, 1999 | 271 | 1999 |
Reactions at polymer–polymer interfaces for blend compatibilization CW Macosko, HK Jeon, TR Hoye Progress in Polymer Science 30 (8-9), 939-947, 2005 | 252 | 2005 |
A simple confined impingement jets mixer for flash nanoprecipitation J Han, Z Zhu, H Qian, AR Wohl, CJ Beaman, TR Hoye, CW Macosko Journal of pharmaceutical sciences 101 (10), 4018-4023, 2012 | 191 | 2012 |
Hybrid Density Functional Methods Empirically Optimized for the Computation of 13C and 1H Chemical Shifts in Chloroform Solution KW Wiitala, TR Hoye, CJ Cramer Journal of Chemical Theory and Computation 2 (4), 1085-1092, 2006 | 187 | 2006 |
Highly efficient synthesis of the potent antitumor annonaceous acetogenin (+)-parviflorin TR Hoye, Z Ye Journal of the American Chemical Society 118 (7), 1801-1802, 1996 | 165 | 1996 |
Synthesis of Stable Block-Copolymer-Protected NaYF4:Yb3+, Er3+ Up-Converting Phosphor Nanoparticles SJ Budijono, J Shan, N Yao, Y Miura, T Hoye, RH Austin, Y Ju, ... Chemistry of Materials 22 (2), 311-318, 2010 | 164 | 2010 |
Flash nanoprecipitation: particle structure and stability KM Pustulka, AR Wohl, HS Lee, AR Michel, J Han, TR Hoye, ... Molecular pharmaceutics 10 (11), 4367-4377, 2013 | 158 | 2013 |
Sustainable thermoplastic elastomers from terpene-derived monomers JM Bolton, MA Hillmyer, TR Hoye ACS Macro Letters 3 (8), 717-720, 2014 | 151 | 2014 |
No-D NMR (no-deuterium proton NMR) spectroscopy: A simple yet powerful method for analyzing reaction and reagent solutions TR Hoye, BM Eklov, TD Ryba, M Voloshin, LJ Yao Organic letters 6 (6), 953-956, 2004 | 151 | 2004 |
Alkane desaturation by concerted double hydrogen atom transfer to benzyne D Niu, PH Willoughby, BP Woods, B Baire, TR Hoye Nature 501 (7468), 531-534, 2013 | 150 | 2013 |
Identification of Sesquiterpene Synthases from Nostoc punctiforme PCC 73102 and Nostoc sp. Strain PCC 7120 SA Agger, F Lopez-Gallego, TR Hoye, C Schmidt-Dannert Journal of bacteriology 190 (18), 6084-6096, 2008 | 150 | 2008 |
A convenient synthesis of dimethyl (diazomethyl) phosphonate (Seyferth/Gilbert reagent) DG Brown, EJ Velthuisen, JR Commerford, RG Brisbois, TR Hoye The Journal of Organic Chemistry 61 (7), 2540-2541, 1996 | 144 | 1996 |
A Strategy for Control of “Random” Copolymerization of Lactide and Glycolide: Application to Synthesis of PEG-b-PLGA Block Polymers Having Narrow Dispersity H Qian, AR Wohl, JT Crow, CW Macosko, TR Hoye Macromolecules 44 (18), 7132-7140, 2011 | 142 | 2011 |