An efficient and stereoselective four step synthesis of (-)-Massoialactone (1) is described. The key step involves deoxygenation of one alpha,beta - unsaturated carbonyl group in compound 5.
4'R, Z, 2-(4'-hydroxy-2'-nonenyl)-1,3-dioxane 2 which is an intermediate in the synthesis of chiral δ-lactones, has been syntheslzed from dlepoxide 3. Enantioselective total synthesis of 6R-(-)-massoialac...4'R, Z, 2-(4'-hydroxy-2'-nonenyl)-1,3-dioxane 2 which is an intermediate in the synthesis of chiral δ-lactones, has been syntheslzed from dlepoxide 3. Enantioselective total synthesis of 6R-(-)-massoialactone 1 has been achieved from 2 through 4 steps展开更多
文摘An efficient and stereoselective four step synthesis of (-)-Massoialactone (1) is described. The key step involves deoxygenation of one alpha,beta - unsaturated carbonyl group in compound 5.
文摘4'R, Z, 2-(4'-hydroxy-2'-nonenyl)-1,3-dioxane 2 which is an intermediate in the synthesis of chiral δ-lactones, has been syntheslzed from dlepoxide 3. Enantioselective total synthesis of 6R-(-)-massoialactone 1 has been achieved from 2 through 4 steps
