Nickel-catalyzed reductive 1,3-diene formation from the cross-coupling of vinyl bromides
作者:Yunfei Sha、Jiandong Liu、Liang Wang、Demin Liang、Da Wu、Hegui Gong
DOI:10.1039/d1ob00791b
日期:——
Facile construction of 1,3-dienes building upon cross-electrophile coupling of two open-chain vinyl halides is disclosed in this work, showing moderate chemoselectivities between the terminal bromoalkenes and internal vinyl bromides. The present method is mild and tolerates a range of functional groups and can be applied to the total synthesis of a tobacco fragrance solanone.
在这项工作中公开了基于两个开链乙烯基卤化物的交叉亲电偶联构建的 1,3-二烯的简易构建,显示末端溴烯烃和内部溴乙烯之间的中等化学选择性。本方法温和,可耐受多种官能团,可应用于烟草香料茄酮的全合成。