Lang, Simon B. published the artcileActivation of Alcohols with Carbon Dioxide: Intermolecular Allylation of Weakly Acidic Pronucleophiles, COA of Formula: C16H13NO, the main research area is nitroalkane allyl alc carbon dioxide palladium allylation catalyst; nitrile allyl alc carbon dioxide palladium allylation catalyst; aldehyde allyl alc carbon dioxide palladium allylation catalyst; allylated product preparation.
The direct coupling of allyl alcs. with nitroalkanes, nitriles, and aldehydes using catalytic Pd(PPh3)4 has been accomplished via activation of C-OH bonds with CO2. The in situ formation of carbonates from alcs. and CO2 facilitates oxidative addition to Pd to form reactive π-allylpalladium intermediates. In addition, the formation of a strong base activates nucleophiles toward the reaction with the π-allylpalladium electrophile. Overall, this atom economical reaction provides a new C-C bond without the use of an external base and generates water as the only byproduct.
Organic Letters published new progress about Alkanes, nitro Role: RCT (Reactant), SPN (Synthetic Preparation), RACT (Reactant or Reagent), PREP (Preparation). 42872-30-0 belongs to class nitriles-buliding-blocks, name is 2-(3-Benzoylphenyl)propanenitrile, and the molecular formula is C16H13NO, COA of Formula: C16H13NO.
Referemce:
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts