Synthesis of seven-membered lactones by regioselective and stereoselective iodolactonization of electron-deficient olefins

A regio- and stereoselective iodolactonization of internal electron-deficient olefinic acids has been reported, which provides a straightforward access to a series of multi-functionalized seven-membered lactones containing two consecutive chiral centers. The ester substituents on the olefins played a key role in achieving high regioselectivity. This result was proved through experiments and DFT calculations. A regio- and stereoselective iodolactonization of electron-deficient olefinic acids has been reported, which provides a straightforward access to seven-membered lactones with two consecutive chiral centers.