Tandem Conjugate Reduction−Aldol Cyclization Using Stryker's Reagent
收藏NIAID Data Ecosystem2026-03-06 收录
下载链接：
https://figshare.com/articles/dataset/Tandem_Conjugate_Reduction_Aldol_Cyclization_Using_Stryker_s_Reagent/3739206
下载链接
链接失效反馈官方服务：
资源简介：
Conjugate reduction by Stryker's reagent to form copper enolates, followed by intramolecular aldol cyclization, successfully generated five-
and six-membered carbocycles in one pot efficiently. This tandem reaction is generally diastereoselective and provides good yields of the
β-hydroxyketones without any dehydration at low temperatures.
创建时间：
2016-08-20
