Abstract: | (R)- and (S)-α-ionone ((R)- and (S)- 1 , resp.) were prepared from (R)- and (S)-α-damascone ((R)- and (S)- 3 , resp.) without racemization in 48% yield employing a new enone transposition. The described transposition is complementary to existing methods whose application is often prohibited by the structural requirements of the substrate. The now easily accessible α-ionones of desired absolute configuration are useful as chiral building blocks for terpenoid synthesis. |