A two-step transition from individual diastereomeric 2,2-dichloro-2-(1,5)- and 2,2-dichloro-2-[(1,5)-5-hydroxycyclopent-2-en-1-yl-N-(1)-1-phenylethylacetamides to the enantiomers of Grieco lactone is described with a total yield of 77%.
Z.R. Valiullina (Wed,) studied this question.