Curran, Dennis P.; Ko, Sung-Bo published the artcile< Synthesis of Optically Active α-Hydroxy Lactones by Sharpless Asymmetric Dihydroxylations of Ketene Acetals, Enol Ethers, and Ene Lactones>, Recommanded Product: (9Z,12Z)-Methyl octadeca-9,12-dienoate, the main research area is Sharpless asym dihydroxylation hydroxy lactone synthesis; ketene acetal Sharpless asym dihydroxylation; enol ether Sharpless asym dihydroxylation; unsaturated lactone Sharpless asym dihydroxylation.
Three different AD routes to optically active α-hydroxy lactones of good to excellent optical purity are reported. The substrates for the AD reaction are endocyclic ketene acetals, endocyclic enol ethers, and exocyclic α,β-unsaturated lactones.
Journal of Organic Chemistry published new progress about Acetals, ketene Role: RCT (Reactant), SPN (Synthetic Preparation), RACT (Reactant or Reagent), PREP (Preparation). 112-63-0 belongs to class esters-buliding-blocks, and the molecular formula is C19H34O2, Recommanded Product: (9Z,12Z)-Methyl octadeca-9,12-dienoate.
Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics