Terlizzi, Lorenzo Di published the artcileDyedauxiliary Group Strategy for the α-Functionalization of Ketones and Esters, Application In Synthesis of 1885-29-6, the main research area is arylketone arylazo ester preparation; arylazo sulfone enol silyl ether ketene acetal activation.
The synthesis of α-arylketones and α-arylazo esters has been achieved in mixed organic-aqueous media under photocatalyst- and metal-free conditions via visible light activation of arylazo sulfones in the presence of enol silyl ethers and ketene silyl acetals, resp. The process took place efficiently and exhibits an excellent tolerance for a broad variety of functional groups.
ACS Organic & Inorganic Au published new progress about Acetals, ketene, silyl Role: RCT (Reactant), RACT (Reactant or Reagent). 1885-29-6 belongs to class nitriles-buliding-blocks, name is 2-Aminobenzonitrile(Flakes or Chunks), and the molecular formula is C7H6N2, Application In Synthesis of 1885-29-6.
Referemce:
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts