ãOrganophotocatalytic N-O Bond Cleavage of Weinreb Amides: Mechanism-Guided Evolution of a PET to ConPET Platformã?was written by Soika, Julia; McLaughlin, Calum; Nevesely, Tomas; Daniliuc, Constantin G.; Molloy, John. J.; Gilmour, Ryan. Recommanded Product: Bis[(pinacolato)boryl]methaneThis research focused onWeinreb amide preparation organophotocatalyst bond cleavage. The article conveys some information:
Mechanistically guided reaction development demonstrates the involvement of a photoinduced electron transfer (PET) mechanism, and this has been further advanced to a consecutive photoinduced electron transfer (ConPET) manifold and this has significantly expanded the scope of compatible substrates RC(O)N(CH3)OCH3 (R = 4-cyanomethyl, pyrazin-2-yl, penta-1,3-dien-1-yl, etc.). The experimental part of the paper was very detailed, including the reaction process of Bis[(pinacolato)boryl]methane(cas: 78782-17-9Recommanded Product: Bis[(pinacolato)boryl]methane)
Bis[(pinacolato)boryl]methane(cas: 78782-17-9) belongs to organoboron compounds.Recommanded Product: Bis[(pinacolato)boryl]methane Organoboron compounds are versatile intermediates and as such are some of the most important classes of reagents in modern organic chemistry. This stems from their ease of preparation combined with their ability to undergo a broad range of chemical transformations.
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