Abstract
Radical vinylation was investigated using vinyl bromides with an electron-withdrawing substituent at the β-position. The vinylation of 1,3-dioxolanes proceeded well to give 2-vinyl-1,3-dioxolanes in good yields. The α-vinylation of N-acylpyrrolidines also proceeded well to give 2-vinyl-N-acylpyrrolidines.
- This article is part of the themed collection: In Celebration of Max Malacria’s 65th Birthday