Seo, Hyowon published the artcileCatalytic Generation and Use of Ketyl Radical from Unactivated Aliphatic Carbonyl Compounds, Quality Control of 539-88-8, the main research area is alc preparation continuous flow batch process; aliphatic ketone aldehyde styrene ketyl radical reductive coupling.
Generation of a ketyl radical from unactivated aliphatic carbonyl compounds is an important strategy in organic synthesis. Herein, catalytic generation and use of a ketyl radical for the reductive coupling of aliphatic carbonyl compounds and styrenes by organic photoredox catalysis is described. This method is applicable to both aliphatic ketones and aldehydes to afford the corresponding tertiary and secondary alcs. in continuous flow and batch. A preliminary mechanistic investigation suggests the catalytic formation of a ketyl radical intermediate.
Organic Letters published new progress about Aliphatic aldehydes Role: RCT (Reactant), RACT (Reactant or Reagent). 539-88-8 belongs to class esters-buliding-blocks, name is Ethyl 4-oxopentanoate, and the molecular formula is C7H12O3, Quality Control of 539-88-8.
Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics