Literatura científica selecionada sobre o tema "Iridium-catalyzed borylation"
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Artigos de revistas sobre o assunto "Iridium-catalyzed borylation"
Shi, Yongjia, Qian Gao e Senmiao Xu. "Iridium-Catalyzed Asymmetric C–H Borylation Enabled by Chiral Bidentate Boryl Ligands". Synlett 30, n.º 19 (28 de outubro de 2019): 2107–12. http://dx.doi.org/10.1055/s-0039-1690225.
Texto completo da fonteChattopadhyay, Buddhadeb, Mirja Md Mahamudul Hassan, Md Emdadul Hoque, Sayan Dey, Saikat Guria e Brindaban Roy. "Iridium-Catalyzed Site-Selective Borylation of 8-Arylquinolines". Synthesis 53, n.º 18 (11 de maio de 2021): 3333–42. http://dx.doi.org/10.1055/a-1506-3884.
Texto completo da fonteChotana, Ghayoor, Soneela Asghar, Tayyaba Shahzadi, Meshari Alazmi, Xin Gao, Abdul-Hamid Emwas, Rahman Saleem e Farhat Batool. "Iridium-Catalyzed Regioselective Borylation of Substituted Biaryls". Synthesis 50, n.º 11 (28 de março de 2018): 2211–20. http://dx.doi.org/10.1055/s-0036-1591968.
Texto completo da fontePan, Zilong, Luhua Liu, Senmiao Xu e Zhenlu Shen. "Ligand-free iridium-catalyzed regioselective C–H borylation of indoles". RSC Advances 11, n.º 10 (2021): 5487–90. http://dx.doi.org/10.1039/d0ra10211c.
Texto completo da fonteEastabrook, Andrew S., e Jonathan Sperry. "Iridium-Catalyzed Triborylation of 3-Substituted Indoles". Australian Journal of Chemistry 68, n.º 12 (2015): 1810. http://dx.doi.org/10.1071/ch15393.
Texto completo da fonteDa Ros, Sara, Anthony Linden, Kim K. Baldridge e Jay S. Siegel. "Boronic esters of corannulene: potential building blocks toward icosahedral supramolecules". Organic Chemistry Frontiers 2, n.º 6 (2015): 626–33. http://dx.doi.org/10.1039/c5qo00009b.
Texto completo da fonteHitosugi, Shunpei, Yuta Nakamura, Taisuke Matsuno, Waka Nakanishi e Hiroyuki Isobe. "Iridium-catalyzed direct borylation of phenacenes". Tetrahedron Letters 53, n.º 9 (fevereiro de 2012): 1180–82. http://dx.doi.org/10.1016/j.tetlet.2011.12.106.
Texto completo da fonteChotana, Ghayoor A., Jose R. Montero Bastidas, Susanne L. Miller, Milton R. Smith e Robert E. Maleczka. "One-Pot Iridium Catalyzed C–H Borylation/Sonogashira Cross-Coupling: Access to Borylated Aryl Alkynes". Molecules 25, n.º 7 (10 de abril de 2020): 1754. http://dx.doi.org/10.3390/molecules25071754.
Texto completo da fonteIshiyama, Tatsuo, e Norio Miyaura. "Iridium-catalyzed borylation of arenes and heteroarenes via C-H activation". Pure and Applied Chemistry 78, n.º 7 (1 de janeiro de 2006): 1369–75. http://dx.doi.org/10.1351/pac200678071369.
Texto completo da fonteWang, Yongpeng, Mengzhu Liu, Yang Sun, Yingshuang Shang, Bo Jiang, Haibo Zhang e Zhenhua Jiang. "Aluminium borate whiskers grafted with boric acid containing poly(ether ether ketone) as a reinforcing agent for the preparation of poly(ether ether ketone) composites". RSC Advances 5, n.º 122 (2015): 100856–64. http://dx.doi.org/10.1039/c5ra19635c.
Texto completo da fonteTeses / dissertações sobre o assunto "Iridium-catalyzed borylation"
Panza, Florian. "Fοnctiοnnalisatiοn directe οrthοgοnale métallο-catalysée des sites carbοne-hydrοgène des platefοrmes pharmacοlοgiques à cοeur imidazοisοindοle". Electronic Thesis or Diss., Normandie, 2024. http://www.theses.fr/2024NORMIR11.
Texto completo da fonteFor several decades, chemists constantly seek to push the limits of synthetic strategies by developing ever more efficient and more economical methodologies. In this context, transition metal-catalyzed direct functionalization of C—H bonds is one of the most powerful tools for constructing and funtionalizing simple molecules and ever more complex moieties, with a great diversity of C—H bonds. These strategies also answer the needs for the opening of the chemical space of functionalization. Imidazoisoindole, tricyclic heterocycle composed of an imidazole core, is a very interesting scaffold for biological activity and presents C—H bonds with very diverse properties, but late-functionalization methodology of these structures has yet to be listed in the literature. This work takes place in this context and presents, (I) based on past laboratory experience, a robust methodology to synthetize diversely substituted imidazoisoindoles at high scale by palladium-catalyzed intramolecular C—H activation ; (II) an extension of standard directC2—H functionalization of 1,3-diazole moieties applied to imidazo[5,1-a]isoindoles with a palladium(0)-copper(I) cooperative catalysis ; (III) a new methodology of direct C(sp³)—H palladium-catalyzed mono-functionalization at benzylic position of imidazo[2,1-a]isoindoles ; (IV) a preliminary study of the observed regioselectivity of iridium-catalyzed direct C(sp²)—H borylation of imidazo[2,1-a]isoindoles
Capítulos de livros sobre o assunto "Iridium-catalyzed borylation"
Morales, Maria, Sean Preshlock, Liam S. Sharninghausen, Jay S. Wright, Allen F. Brooks, Melanie S. Sanford e Peter J. H. Scott. "Tandem Iridium-Catalyzed C–H Borylation/Copper-Mediated Radiofluorination of Aromatic C–H Bonds with [18F]TBAF". In Methods in Molecular Biology, 45–53. New York, NY: Springer US, 2023. http://dx.doi.org/10.1007/978-1-0716-3499-8_4.
Texto completo da fonteFernández, Elena. "Iridium-Catalyzed Undirected Homogeneous C–H Borylation Reaction". In Topics in Organometallic Chemistry. Berlin, Heidelberg: Springer Berlin Heidelberg, 2020. http://dx.doi.org/10.1007/3418_2020_53.
Texto completo da fonte"2.6 C—H Functionalization Catalyzed by Low-Valent Cobalt". In Base-Metal Catalysis 2. Stuttgart: Georg Thieme Verlag KG, 2023. http://dx.doi.org/10.1055/sos-sd-239-00042.
Texto completo da fonte