Crotti, Simone; Di Iorio, Nicola; Artusi, Chiara; Mazzanti, Andrea; Righi, Paolo; Bencivenni, Giorgio published the artcile< Direct Access to Alkylideneoxindoles via Axially Enantioselective Knoevenagel Condensation>, Synthetic Route of 112-63-0, the main research area is cyclohexanone oxindole cinchona alkaloid amine catalyst enantioselective Knoevenagel condensation; cyclohexylidene oxindole stereoselective preparation.
The organocatalytic axially enantioselective Knoevenagel condensation between prochiral cyclohexanones and oxindoles is presented. The reaction, promoted by a primary amine, proceeded smoothly and furnished unprecedented examples of novel cyclohexylidene oxindoles displaying axial chirality, e.g., I.
Organic Letters published new progress about Cyclohexanones Role: RCT (Reactant), RACT (Reactant or Reagent). 112-63-0 belongs to class esters-buliding-blocks, and the molecular formula is C19H34O2, Synthetic Route of 112-63-0.
Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics