114247-78-8Relevant articles and documents
Lead(IV) acetate oxidative ring-opening of 2,3-epoxy primary alcohols: A new entry to optically active α-hydroxy carbonyl compounds
Alvarez-Manzaneda, Enrique,Chahboun, Rachid,Alvarez, Esteban,Alvarez-Manzaneda, Ramón,Mu?oz, Pedro E.,Jiménez, Fermín,Bouanou, Hanane
experimental part, p. 4017 - 4020 (2011/08/21)
The treatment of 2,3-epoxy primary alcohols with lead(IV) acetate (LTA) leads to α-acetoxy aldehydes or α-acetoxy ketones, through the nucleophilic ring-opening of an intermediate oxonium and the subsequent carbon-carbon bond cleavage. This reaction repre
CONCISE ASYMMETRIC SYNTHESIS OF (5S, 6S)- AEGINETOLIDE AND (5S)- DIHYDROACTINIDIOLIDE
Cain, C. M.,Simpkins, N. S.
, p. 3723 - 3724 (2007/10/02)
An asymmetric deprotonation reaction allows for short syntheses of the lactones (5S,6S)- Aeginetolide (1) and (5S)-Dihydroactinidiolide (2).