Metal-free nitro-carbocyclization of 1,6-enynes with tBuONO and TEMPO†
Abstract
A novel and convenient metal-free nitration and cyclization of 1,6-enynes has been developed. Two C–C bonds and one C–N bond were constructed in one process in this reaction. This transformation is proven to have relatively good functional-group applicability and can be scaled up to gram quantities in satisfactory yields. According to the following experimental facts and related literature reports, a radical pathway was involved in this transformation.