| Strategic applications of named reactions in organic synthesis L Kurti, B Czakó Elsevier, 2005 | 1527 | 2005 |
| Strategic applications of named reactions in organic synthesis L Kurti, B Czakó Elsevier, 2005 | 1527 | 2005 |
| Direct stereospecific synthesis of unprotected NH and N-Me aziridines from olefins JL Jat, MP Paudyal, H Gao, QL Xu, M Yousufuddin, D Devarajan, DH Ess, ... Science 343 (6166), 61-65, 2014 | 297 | 2014 |
| Molecules and medicine EJ Corey, B Czakó, L Kürti John Wiley & Sons, 2007 | 277 | 2007 |
| Dirhodium-catalyzed CH arene amination using hydroxylamines MP Paudyal, AM Adebesin, SR Burt, DH Ess, Z Ma, L Kürti, JR Falck Science 353 (6304), 1144-1147, 2016 | 242 | 2016 |
| Organocatalytic aryl–aryl bond formation: an atroposelective [3, 3]-rearrangement approach to BINAM derivatives GQ Li, H Gao, C Keene, M Devonas, DH Ess, L Kürti Journal of the American Chemical Society 135 (20), 7414-7417, 2013 | 238 | 2013 |
| Rapid Synthesis of Fused N‐Heterocycles by Transition‐Metal‐Free Electrophilic Amination of Arene C H Bonds H Gao, QL Xu, M Yousufuddin, DH Ess, L Kürti Angewandte Chemie International Edition 53 (10), 2701-2705, 2014 | 203 | 2014 |
| Symmetry in cascade chirality-transfer processes: a catalytic atroposelective direct arylation approach to BINOL derivatives JZ Wang, J Zhou, C Xu, H Sun, L Kürti, QL Xu Journal of the American Chemical Society 138 (16), 5202-5205, 2016 | 187 | 2016 |
| Elusive metal-free primary amination of arylboronic acids: synthetic studies and mechanism by density functional theory C Zhu, G Li, DH Ess, JR Falck, L Kürti Journal of the American Chemical Society 134 (44), 18253-18256, 2012 | 152 | 2012 |
| Enantioselective chemical synthesis: methods, logic, and practice EJ Corey, L Kurti Elsevier, 2013 | 137 | 2013 |
| Direct and Stereospecific Synthesis of N‐H and N‐Alkyl Aziridines from Unactivated Olefins Using Hydroxylamine‐O‐Sulfonic Acids Z Ma, Z Zhou, L Kürti Angewandte Chemie 129 (33), 10018-10022, 2017 | 119 | 2017 |
| Practical Organocatalytic Synthesis of Functionalized Non‐C2‐Symmetrical Atropisomeric Biaryls H Gao, QL Xu, C Keene, M Yousufuddin, DH Ess, L Kürti Angewandte Chemie 128 (2), 576-581, 2016 | 114 | 2016 |
| New insights into the mechanism of phenolic oxidation with phenyliodonium (III) reagents L Kürti, P Herczegh, J Visy, M Simonyi, S Antus, A Pelter Journal of the Chemical Society, Perkin Transactions 1, 379-380, 1999 | 105 | 1999 |
| Transition-metal-free direct arylation: synthesis of halogenated 2-amino-2′-hydroxy-1, 1′-biaryls and mechanism by DFT calculations H Gao, DH Ess, M Yousufuddin, L Kürti Journal of the American Chemical Society 135 (19), 7086-7089, 2013 | 104 | 2013 |
| Aerobic, transition-metal-free, direct, and regiospecific mono-α-arylation of ketones: synthesis and mechanism by DFT calculations QL Xu, H Gao, M Yousufuddin, DH Ess, L Kürti Journal of the American Chemical Society 135 (38), 14048-14051, 2013 | 95 | 2013 |
| Practical access to axially chiral sulfonamides and biaryl amino phenols via organocatalytic atroposelective N-alkylation S Lu, SVH Ng, K Lovato, JY Ong, SB Poh, XQ Ng, L Kürti, Y Zhao Nature Communications 10 (1), 3061, 2019 | 76 | 2019 |
| Rapid heteroatom transfer to arylmetals utilizing multifunctional reagent scaffolds H Gao, Z Zhou, DH Kwon, J Coombs, S Jones, NE Behnke, DH Ess, ... Nature chemistry 9 (7), 681-688, 2017 | 73 | 2017 |
| A short, scalable synthesis of the carbocyclic core of the anti-angiogenic cortistatins from (+)-estrone by B-ring expansion L Kürti, B Czakó, EJ Corey Organic Letters 10 (22), 5247-5250, 2008 | 72 | 2008 |
| Indole diterpene synthetic studies: development of a second-generation synthetic strategy for (+)-nodulisporic acids A and B AB Smith, L Kürti, AH Davulcu, YS Cho, K Ohmoto The Journal of Organic Chemistry 72 (13), 4611-4620, 2007 | 72 | 2007 |
| Discovery of potent and practical antiangiogenic agents inspired by cortistatin A B Czako, L Kürti, A Mammoto, DE Ingber, EJ Corey Journal of the American Chemical Society 131 (25), 9014-9019, 2009 | 71 | 2009 |
Daniel EssBrigham Young UniversityDirección de correo verificada de chem.byu.edu
