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Mitsunobu Reaction

Professor Dave Explains ↗

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A particularly useful name reaction is the Mitsunobu reaction, which allows for the inversion of secondary alcohols, meaning from one stereochemistry to the other, which can be invaluable for organic synthesis. This will utilize a phosphine and an azodicarboxylate. How does this work? Let's take a look now! Watch the whole Organic Chemistry playlist: http://bit.ly/ProfDaveOrgChem General Chemistry Tutorials: http://bit.ly/ProfDaveGenChem 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► [email protected] 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 Book Depository: http://bit.ly/3aOVDlT

Published 2024-01-10 · Watch on YouTube ↗
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