Regio- and Stereoselective Anti-Carbozincation of Alkynyl Ethers Using ZnBr2 toward (Z)-β-Zincated Enol Ether Synthesis.

(Z)-β-Aryloxyalkenylzincs are synthesized stereoselectively via anti-carbozincation among alkynyl ethers, silyl ketene acetals, and ZnBr2. X-ray analysis revealed the structure of the zinc species is a mononuclear two-coordinate dialkenylzinc that is transformed into functionalized enol ethers as a single isomer in the reaction of various electrophiles.