Hao, Lin; Du, Yu; Lv, Hui; Chen, Xingkuan; Jiang, Huishen; Shao, Yaling; Chi, Yonggui Robin published the artcile< Enantioselective Activation of Stable Carboxylate Esters as Enolate Equivalents via N-Heterocyclic Carbene Catalysts>, SDS of cas: 112-63-0, the main research area is chiral NHC catalyst enantioselective activation carboxylate ester enolate equivalent; unsaturated imine enantioselective cycloaddition carboxylate ester enolate NHC catalyst.
The first N-heterocyclic carbene (NHC) mediated activation of stable carboxylate esters to generate enolate intermediates is disclosed. The catalytically generated arylacetic ester enolates undergo diastereo- and enantioselective [4 + 2]-cycloaddition reactions with α,β-unsaturated imines.
Organic Letters published new progress about Carboxylic esters Role: RCT (Reactant), SPN (Synthetic Preparation), RACT (Reactant or Reagent), PREP (Preparation) (arylacetic esters). 112-63-0 belongs to class esters-buliding-blocks, and the molecular formula is C19H34O2, SDS of cas: 112-63-0.
Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics