Publication Date:
2014
abstract:
1,2-Diols 3 have been synthesized by the aldol addition of hydroxy esters 1 to propargyl aldehydes 2 in dichloromethane. These 1,2-diols undergo a base-initiated rearrangement under mild conditions in methanol with an unusual 1,2-alkyl shift to afford interesting alpha,beta-unsaturated gamma-butyrolactones 4. A possible mechanism is postulated on the basis of experimental evidence and the results of DFT calculations.
Iris type:
01.01 Articolo in rivista
Keywords:
Synthetic methods; Alcohols; Aldehydes; Lactones; Rearrangement; Reaction mechanisms
List of contributors:
Salvio, Riccardo
Published in: