Literatura científica selecionada sobre o tema "Directed borylation"
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Artigos de revistas sobre o assunto "Directed borylation"
Wang, Yan, Le Wang, Ling-Yan Chen, Pinaki S. Bhadury e 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 completo da fonteAl 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 maio de 2024): 318–37. http://dx.doi.org/10.3390/reactions5020016.
Texto completo da fonteIqbal, S. A., K. Yuan, J. Cid, J. Pahl e 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 completo da fonteAuth, Marin R., Kathryn A. McGarry e Timothy B. Clark. "Phosphorus‐Directed C−H Borylation". Advanced Synthesis & Catalysis 363, n.º 9 (30 de março de 2021): 2354–65. http://dx.doi.org/10.1002/adsc.202100173.
Texto completo da fonteCazorla, Clément, Timothy S. De Vries e Edwin Vedejs. "P-Directed Borylation of Phenols". Organic Letters 15, n.º 5 (março de 2013): 984–87. http://dx.doi.org/10.1021/ol303203m.
Texto completo da fonteIqbal, S. A., J. Pahl, K. Yuan e 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 completo da fonteRos, A., R. Fernández e 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 completo da fonteXu, Ming-Hua. "Metal-free directed C–H borylation". Chinese Science Bulletin 65, n.º 5 (1 de fevereiro de 2020): 331–33. http://dx.doi.org/10.1360/tb-2019-0657.
Texto completo da fonteDe Vries, Timothy S., Aleksandrs Prokofjevs, Jeremy N. Harvey e Edwin Vedejs. "Superelectrophilic Intermediates in Nitrogen-Directed Aromatic Borylation". Journal of the American Chemical Society 131, n.º 41 (21 de outubro de 2009): 14679–87. http://dx.doi.org/10.1021/ja905369n.
Texto completo da fonteLv, 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 setembro de 2019): 336–40. http://dx.doi.org/10.1038/s41586-019-1640-2.
Texto completo da fonteTeses / dissertações sobre o assunto "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 completo da fonteDel, 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 completo da fonteBentley, 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 completo da fonteDescribed 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 completo da fonteEliseeva, 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 completo da fonteThe 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 e 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 completo da fonteMartin, 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 completo da fonteLassalas, 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 completo da fonteDue 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 completo da fonteCapítulos de livros sobre o assunto "Directed borylation"
Yang, Y., e C. Wang. "2.15 Manganese-Catalyzed C—H Functionalization". In Base-Metal Catalysis 2. Stuttgart: Georg Thieme Verlag KG, 2023. http://dx.doi.org/10.1055/sos-sd-239-00231.
Texto completo da fonteTaber, Douglass. "Preparation of Benzene Derivatives". In Organic Synthesis. Oxford University Press, 2011. http://dx.doi.org/10.1093/oso/9780199764549.003.0063.
Texto completo da fonteCollier, S. J. "Direct Borylation of Imines (or Enamines)". In 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 completo da fonteMiyaura, N. "Direct Borylation of Alkanes and Arenes". In Boron Compounds, 1. Georg Thieme Verlag KG, 2005. http://dx.doi.org/10.1055/sos-sd-006-00223.
Texto completo da fonteHall, D. G., e H. Zheng. "Synthesis by Direct Borylation with Borenium Cations". In Boron Compounds, 1. Georg Thieme Verlag KG, 2011. http://dx.doi.org/10.1055/sos-sd-106-00009.
Texto completo da fonteTaber, Douglass F. "Substituted Benzenes: The Gu Synthesis of Rhazinal". In Organic Synthesis. Oxford University Press, 2015. http://dx.doi.org/10.1093/oso/9780190200794.003.0065.
Texto completo da fonteTaber, Douglass F. "C–H Functionalization". In Organic Synthesis. Oxford University Press, 2015. http://dx.doi.org/10.1093/oso/9780190200794.003.0021.
Texto completo da fonteTaber, Douglass F. "Enantioselective Preparation of Alcohols and Amines". In Organic Synthesis. Oxford University Press, 2013. http://dx.doi.org/10.1093/oso/9780199965724.003.0036.
Texto completo da fonteTaber, Douglass F. "Enantioselective Synthesis of Alcohols and Amines: The Fujii/Ohno Synthesis of (+)-Lysergic Acid". In Organic Synthesis. Oxford University Press, 2015. http://dx.doi.org/10.1093/oso/9780190200794.003.0035.
Texto completo da fonteTaber, Douglass. "Synthesis of Substituted Benzenes: The Carter Synthesis of Siamenol". In Organic Synthesis. Oxford University Press, 2011. http://dx.doi.org/10.1093/oso/9780199764549.003.0062.
Texto completo da fonte