Literatura académica sobre el tema "Directed borylation"
Crea una cita precisa en los estilos APA, MLA, Chicago, Harvard y otros
Consulte las listas temáticas de artículos, libros, tesis, actas de conferencias y otras fuentes académicas sobre el tema "Directed borylation".
Junto a cada fuente en la lista de referencias hay un botón "Agregar a la bibliografía". Pulsa este botón, y generaremos automáticamente la referencia bibliográfica para la obra elegida en el estilo de cita que necesites: APA, MLA, Harvard, Vancouver, Chicago, etc.
También puede descargar el texto completo de la publicación académica en formato pdf y leer en línea su resumen siempre que esté disponible en los metadatos.
Artículos de revistas sobre el tema "Directed borylation"
Wang, Yan, Le Wang, Ling-Yan Chen, Pinaki S. Bhadury y Zhihua Sun. "Transition Metal-Free Synthesis of Pinacol Arylboronate: Regioselective Boronation of 1,3-Disubstituted Benzenes". Australian Journal of Chemistry 67, n.º 4 (2014): 675. http://dx.doi.org/10.1071/ch13642.
Texto completoAl Mamari, Hamad H. "Ir-Catalyzed ortho-C-H Borylation of Aromatic C(sp2)-H Bonds of Carbocyclic Compounds Assisted by N-Bearing Directing Groups". Reactions 5, n.º 2 (1 de mayo de 2024): 318–37. http://dx.doi.org/10.3390/reactions5020016.
Texto completoIqbal, S. A., K. Yuan, J. Cid, J. Pahl y M. J. Ingleson. "Controlling selectivity in N-heterocycle directed borylation of indoles". Organic & Biomolecular Chemistry 19, n.º 13 (2021): 2949–58. http://dx.doi.org/10.1039/d1ob00018g.
Texto completoAuth, Marin R., Kathryn A. McGarry y Timothy B. Clark. "Phosphorus‐Directed C−H Borylation". Advanced Synthesis & Catalysis 363, n.º 9 (30 de marzo de 2021): 2354–65. http://dx.doi.org/10.1002/adsc.202100173.
Texto completoCazorla, Clément, Timothy S. De Vries y Edwin Vedejs. "P-Directed Borylation of Phenols". Organic Letters 15, n.º 5 (marzo de 2013): 984–87. http://dx.doi.org/10.1021/ol303203m.
Texto completoIqbal, S. A., J. Pahl, K. Yuan y M. J. Ingleson. "Intramolecular (directed) electrophilic C–H borylation". Chemical Society Reviews 49, n.º 13 (2020): 4564–91. http://dx.doi.org/10.1039/c9cs00763f.
Texto completoRos, A., R. Fernández y J. M. Lassaletta. "Functional group directed C–H borylation". Chem. Soc. Rev. 43, n.º 10 (2014): 3229–43. http://dx.doi.org/10.1039/c3cs60418g.
Texto completoXu, Ming-Hua. "Metal-free directed C–H borylation". Chinese Science Bulletin 65, n.º 5 (1 de febrero de 2020): 331–33. http://dx.doi.org/10.1360/tb-2019-0657.
Texto completoDe Vries, Timothy S., Aleksandrs Prokofjevs, Jeremy N. Harvey y Edwin Vedejs. "Superelectrophilic Intermediates in Nitrogen-Directed Aromatic Borylation". Journal of the American Chemical Society 131, n.º 41 (21 de octubre de 2009): 14679–87. http://dx.doi.org/10.1021/ja905369n.
Texto completoLv, Jiahang, Xiangyang Chen, Xiao-Song Xue, Binlin Zhao, Yong Liang, Minyan Wang, Liqun Jin et al. "Metal-free directed sp2-C–H borylation". Nature 575, n.º 7782 (30 de septiembre de 2019): 336–40. http://dx.doi.org/10.1038/s41586-019-1640-2.
Texto completoTesis sobre el tema "Directed borylation"
Crossley, Daniel. "Directed C-H borylation for the synthesis of fused and ladder type conjugated oligomers and polymers". Thesis, University of Manchester, 2016. https://www.research.manchester.ac.uk/portal/en/theses/directed-ch-borylation-for-the-synthesis-of-fused-and-ladder-type-conjugated-oligomers-and-polymers(8c96a89b-7442-41f3-839b-56148b5fd458).html.
Texto completoDel, Grosso Alessandro. "Borenium cations for the direct electrophilic borylation of arenes". Thesis, University of Manchester, 2013. https://www.research.manchester.ac.uk/portal/en/theses/borenium-cations-for-the-direct-electrophilic-borylation-of-arenes(a505cdb2-08fe-43a0-ad0b-86ab357fadd1).html.
Texto completoBentley, Sierra Kathleen. "Selective Direct Borylation and Late-Stage Functionalization of 1,2-Azaborines:". Thesis, Boston College, 2020. http://hdl.handle.net/2345/bc-ir:109014.
Texto completoDescribed herein is the development of a method to directly borylate the C5-position of monocyclic 1,2-azaborines without the use of a metal catalyst, kinetic resolution or directing group. This method tolerates different substitution on the boron as well as at the C3-position of the azaborine. A new BN-isostere of the drug molecule, felbinac, was synthesized to demonstrate the application of this method
Thesis (MS) — Boston College, 2020
Submitted to: Boston College. Graduate School of Arts and Sciences
Discipline: Chemistry
Coapes, Richard Benjamin. "Rhodium catalysed borylation reactions via direct and indirect C-H activation". Thesis, Durham University, 2002. http://etheses.dur.ac.uk/4176/.
Texto completoEliseeva, Maria N. "New Route to a [5,5] Carbon Nanotube End-Cap via Direct Borylation of Corannulene". Thesis, Boston College, 2011. http://hdl.handle.net/2345/2752.
Texto completoThe Scott lab is interested in the functionalization of corannulene as a building block for large polycyclic aromatic hydrocarbons and carbon nanotube end-cap precursors. Toward that end, a new approach to the direct five-fold borylation of corannulene with iridium (I) catalysts via C-H activation has been explored. It has been discovered that the addition of catalytic amounts of base to the reaction mixture promotes the formation of symmetrical penta-borylated corannulene in a good yield on a sizable scale. All byproducts can be easily removed with iterative methanol washes. The present work also provides proof of the reversibility of the direct borylation reaction under the conditions used. Furthermore, modified Suzuki-Miyaura conditions have been employed to synthesize pentakis(2,6-dichlorophenyl)corannulene, a precursor for a [5,5] carbon nanotube end-cap. The reported reactions provide good yields and are scalable
Thesis (MS) — Boston College, 2011
Submitted to: Boston College. Graduate School of Arts and Sciences
Discipline: Chemistry
Mori, Goro, Hiroshi Shinokubo y Atsuhiro Osuka. "Highly selective Ir-catalyzed direct sixfold borylation of peripheral aromatic substituents on hexakisaryl-substituted [28]hexaphyrin(1.1.1.1.1.1)". Elsevier, 2008. http://hdl.handle.net/2237/12313.
Texto completoMartin, Thibaut. "Etude de nouvelles méthodologies d'hétéroarylation directe de liaison C-Het C-Br en série thiazolique : application à la synthèse de coeurs thiazolylpyridiniques des thiopeptides de la série d". Phd thesis, INSA de Rouen, 2010. http://tel.archives-ouvertes.fr/tel-00577166.
Texto completoLassalas, Pierrik. "Étude de nouvelles méthodologies d’arylation directe en séries azole et pyridine : Application à la synthèse de coeurs de thiopeptides antibiotiques de la série d". Thesis, Rouen, INSA, 2012. http://www.theses.fr/2012ISAM0024/document.
Texto completoDue to the emergence of multiresistant bacterial strains to standard antibacterial treatments, thiopeptides antibiotics are actually highly considered, though they are known for 60 years. They show an excellent antibiotic activity against multiresistant bacterial strains, and implement two originals inhibition mechanisms of protein synthesis, still unemployed in human therapy. However, the difficulty to prepare these complex macromolecules limits their pharmacological development. The development of a new strategy to synthetize the most complicated part of these macromolecules, their heterocyclic core, is studied here in. This approach is based on the study and the exploitation of novel direct C-H and C-X transition-metal-catalyzed couplings of mono- and bithiazoles units with a broad panel of heteroaromatics. Its viability is here demonstrated trough the multi-step synthesis of the common heterocyclic core of amythiamicins
Lassalas, Pierrik. "Étude de nouvelles méthodologies d'arylation directe en séries azole et pyridine : Application à la synthèse de coeurs de thiopeptides antibiotiques de la série d". Phd thesis, INSA de Rouen, 2012. http://tel.archives-ouvertes.fr/tel-00857574.
Texto completoCapítulos de libros sobre el tema "Directed borylation"
Yang, Y. y C. Wang. "2.15 Manganese-Catalyzed C—H Functionalization". En Base-Metal Catalysis 2. Stuttgart: Georg Thieme Verlag KG, 2023. http://dx.doi.org/10.1055/sos-sd-239-00231.
Texto completoTaber, Douglass. "Preparation of Benzene Derivatives". En Organic Synthesis. Oxford University Press, 2011. http://dx.doi.org/10.1093/oso/9780199764549.003.0063.
Texto completoCollier, S. J. "Direct Borylation of Imines (or Enamines)". En Ene-X Compounds (X=S, Se, Te, N, P), 1. Georg Thieme Verlag KG, 2007. http://dx.doi.org/10.1055/sos-sd-033-00571.
Texto completoMiyaura, N. "Direct Borylation of Alkanes and Arenes". En Boron Compounds, 1. Georg Thieme Verlag KG, 2005. http://dx.doi.org/10.1055/sos-sd-006-00223.
Texto completoHall, D. G. y H. Zheng. "Synthesis by Direct Borylation with Borenium Cations". En Boron Compounds, 1. Georg Thieme Verlag KG, 2011. http://dx.doi.org/10.1055/sos-sd-106-00009.
Texto completoTaber, Douglass F. "Substituted Benzenes: The Gu Synthesis of Rhazinal". En Organic Synthesis. Oxford University Press, 2015. http://dx.doi.org/10.1093/oso/9780190200794.003.0065.
Texto completoTaber, Douglass F. "C–H Functionalization". En Organic Synthesis. Oxford University Press, 2015. http://dx.doi.org/10.1093/oso/9780190200794.003.0021.
Texto completoTaber, Douglass F. "Enantioselective Preparation of Alcohols and Amines". En Organic Synthesis. Oxford University Press, 2013. http://dx.doi.org/10.1093/oso/9780199965724.003.0036.
Texto completoTaber, Douglass F. "Enantioselective Synthesis of Alcohols and Amines: The Fujii/Ohno Synthesis of (+)-Lysergic Acid". En Organic Synthesis. Oxford University Press, 2015. http://dx.doi.org/10.1093/oso/9780190200794.003.0035.
Texto completoTaber, Douglass. "Synthesis of Substituted Benzenes: The Carter Synthesis of Siamenol". En Organic Synthesis. Oxford University Press, 2011. http://dx.doi.org/10.1093/oso/9780199764549.003.0062.
Texto completo