Diastereoselective Synthesis of Functionalized Spirocyclopropyl Oxindoles via P(NMe2)3‑Mediated Reductive Cyclopropanation
收藏Figshare2016-02-16 更新2026-04-29 收录
下载链接：
https://figshare.com/articles/dataset/Diastereoselective_Synthesis_of_Functionalized_Spirocyclopropyl_Oxindoles_via_P_NMe_sub_2_sub_sub_3_sub_Mediated_Reductive_Cyclopropanation/2237833
下载链接
链接失效反馈官方服务：
资源简介：
A P(NMe2)3-mediated reductive cyclopropanation reaction of α-keto esters or amides with isatin-derived alkenes has been developed, providing efficient and diastereoselective synthesis of highly functionalized spirocyclopropyl oxindoles bearing two all-carbon quaternary centers. This reaction also represents a complementary and nonmetal-involving protocol for the challenging cyclopropanation of electron-deficient alkenes.
创建时间：
2016-02-16
