作者:Daniel L. Priebbenow、Robert. W. Gable、Jonathan Baell
DOI:10.1021/acs.joc.5b00250
日期:2015.5.1
A new method for the regioselective and stereoselective iodoacyloxylation of alkynes has been developed. This protocol utilizes a combination of an iodobenzene dicarboxylate and iodine to functionalize a series of activated and unactivated alkynes in an entirely selective and predictable fashion. The resultant iodo-enol ester were subsequently coupled with boronic acids to afford tetrasubstitute alkene derivatives, which could be further converted to the corresponding 1,1-disubstituted acetophenone.