Literatura académica sobre el tema "Migita-Kosugi-Stille"
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 "Migita-Kosugi-Stille".
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 "Migita-Kosugi-Stille"
Peng, Li-fen, Bing-hao Wang, Ming Wang, Zi-long Tang, Yan-zi Jiang, Yin-chun Jiao y Xin-hua Xu. "A One-Pot Method for the Synthesis of Phenylalkynyl-Substituted Terminal Alkynes by Deprotection/Stannylation followed by a Migita–Kosugi–Stille coupling". Journal of Chemical Research 42, n.º 5 (1 de mayo de 2018): 235–38. http://dx.doi.org/10.3184/174751918x15258743466204.
Texto completoWang, Aohan, Masanori Toyofuku, Nobuhiko Nomura y Hiromasa Goto. "Quorum Sensing Materials as New Ligand for Palladium Catalyzed Migita-Kosugi-Stille Polycondensation". International Letters of Chemistry, Physics and Astronomy 32 (abril de 2014): 62–70. http://dx.doi.org/10.18052/www.scipress.com/ilcpa.32.62.
Texto completoWang, Aohan, Masanori Toyofuku, Nobuhiko Nomura y Hiromasa Goto. "Quorum Sensing Materials as New Ligand for Palladium Catalyzed Migita-Kosugi-Stille Polycondensation". International Letters of Chemistry, Physics and Astronomy 32 (22 de abril de 2014): 62–70. http://dx.doi.org/10.56431/p-kk1e9q.
Texto completoNagaki, Aiichiro y Yosuke Ashikari. "Homogeneous Catalyzed Aryl–Aryl Cross-Couplings in Flow". Synthesis 53, n.º 11 (18 de enero de 2021): 1879–88. http://dx.doi.org/10.1055/a-1360-7798.
Texto completoWang, Xiu, Zhenhua Wang, Li Liu, Yuya Asanuma y Yasushi Nishihara. "Nickel-Catalyzed Decarbonylative Stannylation of Acyl Fluorides under Ligand-Free Conditions". Molecules 24, n.º 9 (28 de abril de 2019): 1671. http://dx.doi.org/10.3390/molecules24091671.
Texto completoIshikawa, Takumi, Mako Murata, Hiroshi Masai, Tomohiro Iwai y Jun Terao. "Irradiation with UV Light Accelerates the Migita–Kosugi–Stille Coupling Reaction in Air". Chemistry Letters 51, n.º 2 (5 de febrero de 2022): 124–26. http://dx.doi.org/10.1246/cl.210665.
Texto completoYano, Hiroki, Yui Nakajima y Yasushi Obora. "N,N-Dimethylformamide-stabilized palladium nanoclusters as catalyst for Migita–Kosugi–Stille cross-coupling reactions". Journal of Organometallic Chemistry 745-746 (noviembre de 2013): 258–61. http://dx.doi.org/10.1016/j.jorganchem.2013.08.004.
Texto completoCampos, Joana F. y Sabine Berteina-Raboin. "Eucalyptol as bio-based solvent for Migita–Kosugi–Stille coupling reaction on O,S,N-heterocycle". Catalysis Today 358 (diciembre de 2020): 138–42. http://dx.doi.org/10.1016/j.cattod.2019.11.004.
Texto completoAnsari, Nurul N., Matthew M. Cummings y Björn C. G. Söderberg. "Chemoselectivity in the Kosugi-Migita-Stille coupling of bromophenyl triflates and bromo-nitrophenyl triflates with (ethenyl)tributyltin". Tetrahedron 74, n.º 21 (mayo de 2018): 2547–60. http://dx.doi.org/10.1016/j.tet.2018.02.051.
Texto completoYano, Hiroki, Yui Nakajima y Yasushi Obora. "ChemInform Abstract: N,N-Dimethylformamide-Stabilized Palladium Nanoclusters as Catalyst for Migita-Kosugi-Stille Cross-Coupling Reactions." ChemInform 45, n.º 14 (21 de marzo de 2014): no. http://dx.doi.org/10.1002/chin.201414040.
Texto completoTesis sobre el tema "Migita-Kosugi-Stille"
Abuduaini, Tuniyazi. "Génération de nouveaux acyclonucléosides phosphonates oléfiniques et 1-C-arylglycosides". Electronic Thesis or Diss., Orléans, 2021. http://www.theses.fr/2021ORLE3200.
Texto completoNucleosides and their analogues constitute the main family of antivirals and anticancer drugs. They provide an extremely powerful tool in effectively combating viral infections associated with many viruses such as HIV, HBV, HCV, CMV, VZV and HSV; they have been at the center of antiviral therapy for more than half a century with around 40 compounds approved by the FDA. Viral infections still represent a large public health problem due to the emergence of new viruses, the appearance of resistance to current antivirals and phenomena of viral mutations. This is why the design and synthesis of new antivirals are still relevant today. In the first part of this manuscript, in order to develop new, more active and safe antivirals, we firstly designed and synthesized two new families of olefinic acyclonucleosides phosphonates under prodrug form by modifying the nucleobase, the acyclic chain and the biolabile group. To do this, we used the cross-metathesis reaction as the key step. In the second part, the "scope" of Migita-Kosugi-Stille cross couplings was explored using stannylated iminoalditols and a small library of variously substituted aroyl chloride. More interestingly, the process of formation of the C‒C bond is stereoretentive. New analogs of C‒glycosylated N‒acetylglucosamine were then prepared by a reaction sequence of reduction, deprotection, mesylation and cyclization
Capítulos de libros sobre el tema "Migita-Kosugi-Stille"
Alonso, D. A. y C. Nájera. "Kosugi–Migita–Stille Coupling". En Water in Organic Synthesis, 1. Georg Thieme Verlag KG, 2012. http://dx.doi.org/10.1055/sos-sd-206-00405.
Texto completoAlonso, D. A. y C. Nájera. "The Kosugi–Migita–Stille Reaction". En Monocyclic Arenes, Quasiarenes, and Annulenes, 1. Georg Thieme Verlag KG, 2010. http://dx.doi.org/10.1055/sos-sd-045-00182.
Texto completo