Добірка наукової літератури з теми "Migita-Kosugi-Stille"
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Статті в журналах з теми "Migita-Kosugi-Stille"
Peng, Li-fen, Bing-hao Wang, Ming Wang, Zi-long Tang, Yan-zi Jiang, Yin-chun Jiao, and 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, no. 5 (May 1, 2018): 235–38. http://dx.doi.org/10.3184/174751918x15258743466204.
Повний текст джерелаWang, Aohan, Masanori Toyofuku, Nobuhiko Nomura, and Hiromasa Goto. "Quorum Sensing Materials as New Ligand for Palladium Catalyzed Migita-Kosugi-Stille Polycondensation." International Letters of Chemistry, Physics and Astronomy 32 (April 2014): 62–70. http://dx.doi.org/10.18052/www.scipress.com/ilcpa.32.62.
Повний текст джерелаWang, Aohan, Masanori Toyofuku, Nobuhiko Nomura, and Hiromasa Goto. "Quorum Sensing Materials as New Ligand for Palladium Catalyzed Migita-Kosugi-Stille Polycondensation." International Letters of Chemistry, Physics and Astronomy 32 (April 22, 2014): 62–70. http://dx.doi.org/10.56431/p-kk1e9q.
Повний текст джерелаNagaki, Aiichiro, and Yosuke Ashikari. "Homogeneous Catalyzed Aryl–Aryl Cross-Couplings in Flow." Synthesis 53, no. 11 (January 18, 2021): 1879–88. http://dx.doi.org/10.1055/a-1360-7798.
Повний текст джерелаWang, Xiu, Zhenhua Wang, Li Liu, Yuya Asanuma, and Yasushi Nishihara. "Nickel-Catalyzed Decarbonylative Stannylation of Acyl Fluorides under Ligand-Free Conditions." Molecules 24, no. 9 (April 28, 2019): 1671. http://dx.doi.org/10.3390/molecules24091671.
Повний текст джерелаIshikawa, Takumi, Mako Murata, Hiroshi Masai, Tomohiro Iwai, and Jun Terao. "Irradiation with UV Light Accelerates the Migita–Kosugi–Stille Coupling Reaction in Air." Chemistry Letters 51, no. 2 (February 5, 2022): 124–26. http://dx.doi.org/10.1246/cl.210665.
Повний текст джерелаYano, Hiroki, Yui Nakajima, and Yasushi Obora. "N,N-Dimethylformamide-stabilized palladium nanoclusters as catalyst for Migita–Kosugi–Stille cross-coupling reactions." Journal of Organometallic Chemistry 745-746 (November 2013): 258–61. http://dx.doi.org/10.1016/j.jorganchem.2013.08.004.
Повний текст джерелаCampos, Joana F., and Sabine Berteina-Raboin. "Eucalyptol as bio-based solvent for Migita–Kosugi–Stille coupling reaction on O,S,N-heterocycle." Catalysis Today 358 (December 2020): 138–42. http://dx.doi.org/10.1016/j.cattod.2019.11.004.
Повний текст джерелаAnsari, Nurul N., Matthew M. Cummings, and Björn C. G. Söderberg. "Chemoselectivity in the Kosugi-Migita-Stille coupling of bromophenyl triflates and bromo-nitrophenyl triflates with (ethenyl)tributyltin." Tetrahedron 74, no. 21 (May 2018): 2547–60. http://dx.doi.org/10.1016/j.tet.2018.02.051.
Повний текст джерелаYano, Hiroki, Yui Nakajima, and Yasushi Obora. "ChemInform Abstract: N,N-Dimethylformamide-Stabilized Palladium Nanoclusters as Catalyst for Migita-Kosugi-Stille Cross-Coupling Reactions." ChemInform 45, no. 14 (March 21, 2014): no. http://dx.doi.org/10.1002/chin.201414040.
Повний текст джерелаДисертації з теми "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.
Повний текст джерелаNucleosides 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
Частини книг з теми "Migita-Kosugi-Stille"
Alonso, D. A., and C. Nájera. "Kosugi–Migita–Stille Coupling." In Water in Organic Synthesis, 1. Georg Thieme Verlag KG, 2012. http://dx.doi.org/10.1055/sos-sd-206-00405.
Повний текст джерелаAlonso, D. A., and C. Nájera. "The Kosugi–Migita–Stille Reaction." In Monocyclic Arenes, Quasiarenes, and Annulenes, 1. Georg Thieme Verlag KG, 2010. http://dx.doi.org/10.1055/sos-sd-045-00182.
Повний текст джерела