Stille Reaction
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We are now familiar with C-C cross coupling, and with the Suzuki reaction understood, let's move on to the Stille reaction. This reaction utilizes organostannanes to achieve coupling. Let's take a look! Watch the whole Inorganic/Organometallic Chemistry playlist: http://bit.ly/ProfDaveInorganic General Chemistry Tutorials: http://bit.ly/ProfDaveGenChem Organic Chemistry Tutorials: http://bit.ly/ProfDaveOrgChem Biochemistry Tutorials: http://bit.ly/ProfDaveBiochem Biology Tutorials: http://bit.ly/ProfDaveBio Classical Physics Tutorials: http://bit.ly/ProfDavePhysics1 Modern Physics Tutorials: http://bit.ly/ProfDavePhysics2 Mathematics Tutorials: http://bit.ly/ProfDaveMath EMAIL► ProfessorDaveExplains@gmail.com PATREON► http://patreon.com/ProfessorDaveExplains Check out "Is This Wi-Fi Organic?", my book on disarming pseudoscience! Amazon: https://amzn.to/2HtNpVH Bookshop: https://bit.ly/39cKADM Barnes and Noble: https://bit.ly/3pUjmrn
Tags: stille reaction, organometallic catalysis, john k. stille, organostannanes, cross coupling, tin catalyst, rapamycin, trialkyltin halide, gregory fu, anny jutand, buchwald ligands
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