The Meyer–Schuster rearrangement for the synthesis of α, β-unsaturated carbonyl compounds DA Engel, GB Dudley Organic & biomolecular chemistry 7 (20), 4149-4158, 2009 | 299 | 2009 |
On the existence of and mechanism for microwave-specific reaction rate enhancement GB Dudley, R Richert, AE Stiegman Chemical science 6 (4), 2144-2152, 2015 | 274 | 2015 |
Olefination of ketones using a gold (III)-catalyzed Meyer− Schuster rearrangement DA Engel, GB Dudley Organic Letters 8 (18), 4027-4029, 2006 | 236 | 2006 |
Mix-and-heat benzylation of alcohols using a bench-stable pyridinium salt KWC Poon, GB Dudley The Journal of organic chemistry 71 (10), 3923-3927, 2006 | 175 | 2006 |
Moderating strain without sacrificing reactivity: design of fast and tunable noncatalyzed alkyne–azide cycloadditions via stereoelectronically controlled transition state … B Gold, GB Dudley, IV Alabugin Journal of the American Chemical Society 135 (4), 1558-1569, 2013 | 155 | 2013 |
Selective transition state stabilization via hyperconjugative and conjugative assistance: stereoelectronic concept for copper-free click chemistry B Gold, NE Shevchenko, N Bonus, GB Dudley, IV Alabugin The Journal of organic chemistry 77 (1), 75-89, 2012 | 137 | 2012 |
On the rational design of microwave-actuated organic reactions MR Rosana, Y Tao, AE Stiegman, GB Dudley Chemical Science 3 (4), 1240-1244, 2012 | 127 | 2012 |
Correspondence on microwave effects in organic synthesis. GB Dudley, AE Stiegman, MR Rosana Angewandte Chemie International Edition 52 (31), 2013 | 125 | 2013 |
Microwave-specific acceleration of a Friedel–Crafts reaction: evidence for selective heating in homogeneous solution MR Rosana, J Hunt, A Ferrari, TA Southworth, Y Tao, AE Stiegman, ... The Journal of organic chemistry 79 (16), 7437-7450, 2014 | 109 | 2014 |
Total synthesis of guanacastepene a: a route to enantiomeric control M Mandal, H Yun, GB Dudley, S Lin, DS Tan, SJ Danishefsky The Journal of Organic Chemistry 70 (26), 10619-10637, 2005 | 109 | 2005 |
Tandem nucleophilic addition/fragmentation reactions and synthetic versatility of vinylogous acyl triflates S Kamijo, GB Dudley Journal of the American Chemical Society 128 (19), 6499-6507, 2006 | 96 | 2006 |
A Stereoselective Route to Guanacastepene A through a Surprising Epoxidation This work was supported by the National Institutes of Health (CA-28824). SL is a US Army breast … S Lin, GB Dudley, DS Tan, SJ Danishefsky Angewandte Chemie 114 (12), 2292, 2002 | 93 | 2002 |
Parameters affecting the microwave-specific acceleration of a chemical reaction PK Chen, MR Rosana, GB Dudley, AE Stiegman The Journal of organic chemistry 79 (16), 7425-7436, 2014 | 88 | 2014 |
Oxidation of carbon− silicon bonds: the dramatic advantage of strained siletanes JD Sunderhaus, H Lam, GB Dudley Organic Letters 5 (24), 4571-4573, 2003 | 88 | 2003 |
Total synthesis of (−)-ascochlorin via a cyclobutenone-based benzannulation strategy GB Dudley, KS Takaki, DD Cha, RL Danheiser Organic Letters 2 (21), 3407-3410, 2000 | 88 | 2000 |
Stereocontrol of 5, 5-spiroketals in the synthesis of Cephalosporolide H epimers SF Tlais, GB Dudley Organic Letters 12 (20), 4698-4701, 2010 | 81 | 2010 |
Generation of medium-ring cycloalkynes by ring expansion of vinylogous acyl triflates J Tummatorn, GB Dudley Organic Letters 13 (6), 1572-1575, 2011 | 76 | 2011 |
Lewis acid-catalyzed Meyer–Schuster reactions: Methodology for the olefination of aldehydes and ketones DA Engel, SS Lopez, GB Dudley Tetrahedron 64 (29), 6988-6996, 2008 | 76 | 2008 |
Synthesis of the Functionalized Tricyclic Skeleton of Guanacastepene A: A Tandem Epoxide-Opening β-Elimination/Knoevenagel Cyclization This work was supported by the National … DS Tan, GB Dudley, SJ Danishefsky Angewandte Chemie 114 (12), 2289, 2002 | 76 | 2002 |
A four-step synthesis of the hydroazulene core of guanacastepene GB Dudley, SJ Danishefsky Organic letters 3 (15), 2399-2402, 2001 | 75 | 2001 |