| Factors impacting the mechanism of the mono-N-protected amino acid ligand-assisted and directing-group-mediated C–H activation catalyzed by Pd (II) complex BE Haines, DG Musaev ACS Catalysis 5 (2), 830-840, 2015 | 81 | 2015 |
| The increasingly complex mechanism of HMG-CoA reductase BE Haines, O Wiest, CV Stauffacher Accounts of chemical research 46 (11), 2416-2426, 2013 | 79 | 2013 |
| Flexible Reaction Pocket on Bulky Diphosphine–Ir Complex Controls Regioselectivity in para-Selective C–H Borylation of Arenes BE Haines, Y Saito, Y Segawa, K Itami, DG Musaev ACS Catalysis 6 (11), 7536-7546, 2016 | 78 | 2016 |
| Factors controlling stability and reactivity of dimeric Pd (II) complexes in C–H functionalization catalysis BE Haines, JF Berry, JQ Yu, DG Musaev ACS Catalysis 6 (2), 829-839, 2016 | 66 | 2016 |
| A role for Pd (IV) in catalytic enantioselective C–H functionalization with monoprotected amino acid ligands under mild conditions RE Plata, DE Hill, BE Haines, DG Musaev, L Chu, DP Hickey, MS Sigman, ... Journal of the American Chemical Society 139 (27), 9238-9245, 2017 | 64 | 2017 |
| Mechanistic Details of Pd(II)-Catalyzed C–H Iodination with Molecular I2: Oxidative Addition vs Electrophilic Cleavage BE Haines, H Xu, P Verma, XC Wang, JQ Yu, DG Musaev Journal of the American Chemical Society 137 (28), 9022-9031, 2015 | 64 | 2015 |
| Variable active site loop conformations accommodate the binding of macrocyclic largazole analogues to HDAC8 C Decroos, DJ Clausen, BE Haines, O Wiest, RM Williams, ... Biochemistry 54 (12), 2126-2135, 2015 | 63 | 2015 |
| Cu-Catalyzed aromatic C–H imidation with N-fluorobenzenesulfonimide: mechanistic details and predictive models BE Haines, T Kawakami, K Kuwata, K Murakami, K Itami, DG Musaev Chemical Science 8 (2), 988-1001, 2017 | 58 | 2017 |
| Tailored quinones support high-turnover Pd catalysts for oxidative C–H arylation with O2 CA Salazar, KN Flesch, BE Haines, PS Zhou, DG Musaev, SS Stahl Science 370 (6523), 1454-1460, 2020 | 53 | 2020 |
| Mono-N-protected amino acid ligands stabilize dimeric palladium (II) complexes of importance to C–H functionalization JJ Gair, BE Haines, AS Filatov, DG Musaev, JC Lewis Chemical Science 8 (8), 5746-5756, 2017 | 53 | 2017 |
| The mechanism of directed Ni (II)-catalyzed C–H iodination with molecular iodine BE Haines, JQ Yu, DG Musaev Chemical Science 9 (5), 1144-1154, 2018 | 42 | 2018 |
| Enantioselectivity model for Pd-catalyzed C–H functionalization mediated by the mono-N-protected amino acid (MPAA) family of ligands BE Haines, JQ Yu, DG Musaev ACS Catalysis 7 (7), 4344-4354, 2017 | 42 | 2017 |
| Molecular modeling of the reaction pathway and hydride transfer reactions of HMG-CoA reductase BE Haines, CN Steussy, CV Stauffacher, O Wiest Biochemistry 51 (40), 7983-7995, 2012 | 41 | 2012 |
| Modular synthesis and biological activity of pyridyl-based analogs of the potent class I histone deacetylase inhibitor largazole DJ Clausen, WB Smith, BE Haines, O Wiest, JE Bradner, RM Williams Bioorganic & medicinal chemistry 23 (15), 5061-5074, 2015 | 38 | 2015 |
| Understanding regiodivergence in a Pd (II)-mediated site-selective C–H alkynylation K Usui, BE Haines, DG Musaev, R Sarpong ACS Catalysis 8 (5), 4516-4527, 2018 | 35 | 2018 |
| SET-Induced Biaryl Cross-Coupling: An SRN1 Reaction BE Haines, O Wiest The Journal of Organic Chemistry 79 (6), 2771-2774, 2014 | 33 | 2014 |
| The first Cu-and amine-free Sonogashira-type cross-coupling in the C-6-alkynylation of protected 2′-deoxyadenosine FN Ngassa, EA Lindsey, BE Haines Tetrahedron 65 (21), 4085-4091, 2009 | 33 | 2009 |
| Di-palladium complexes are active catalysts for mono-N-protected amino acid-accelerated enantioselective C–H functionalization JJ Gair, BE Haines, AS Filatov, DG Musaev, JC Lewis ACS Catalysis 9 (12), 11386-11397, 2019 | 28 | 2019 |
| Synthesis of [3a, 7a]-dihydroindoles by a tandem arene cyclopropanation/3, 5-sigmatropic rearrangement reaction SM Wilkerson-Hill, BE Haines, DG Musaev, HML Davies The Journal of organic chemistry 83 (15), 7939-7949, 2018 | 21 | 2018 |
| Synergistic Brønsted/Lewis acid catalyzed aromatic alkylation with unactivated tertiary alcohols or di-tert-butylperoxide to synthesize quaternary carbon centers A Pan, M Chojnacka, R Crowley, L Göttemann, BE Haines, KGM Kou Chemical Science 13 (12), 3539-3548, 2022 | 20 | 2022 |
Djamaladdin MusaevDirector, Emerson Center, Emory UniversityZweryfikowany adres z emory.edu