School of Biotechnology and Health Sciences, Wuyi University, Jiangmen, Guangdong Province 529090, China.
Org Lett. 2022 Mar 4;24(8):1620-1625. doi: 10.1021/acs.orglett.2c00124. Epub 2022 Feb 23.
Diverse substituted pyridines and pyrimidines with high selectivity were obtained using a concise and efficient protocol developed herein. The reaction proceeds via metal-free cascade annulation of isopropene derivatives. Using isopropene derivatives as C3 synthons, NHI as the "N" source, and formaldehyde or dimethyl sulfoxide as the carbon source, this reaction realizes the efficient formation of intermolecular C-N and C-C bonds.
本文发展了一种简洁高效的方法,高选择性地得到了多种取代的吡啶和嘧啶衍生物。该反应通过无金属级联环化异丙烯衍生物进行。以异丙烯衍生物作为 C3 合成子,NHI 作为“N”源,甲醛或二甲亚砜作为碳源,该反应实现了分子间 C-N 和 C-C 键的高效形成。