Cu(I)/Pd(0) cooperative catalysis enabled regioselective C(sp2)-carboboration of 1,3-diynes†
Abstract
We present a regioselective C(sp2)-carboboration of 1,3-diynes using Cu(I)/Pd(0) cooperative catalysis, enabling access to a diverse range of conjugated aryl-substituted boryl enynes. Furthermore, sequential proto-/carbo-/di-boration strategies afforded highly conjugated multi-boron-substituted dienes. Cross-coupling of the boron end groups facilitated the modular synthesis of highly conjugated enynes and dienes with intriguing properties.