Pt-Catalyzed Tandem Epoxide Fragmentation/Pentannulation of Propargylic Esters
收藏NIAID Data Ecosystem2026-03-06 收录
数据链接：
官方服务：
资源简介：
A Pt-catalyzed pentannulation of propargylic esters containing an epoxide moiety has been developed. The present transformation achieves the formation of cyclopentenone products as single diastereomers in good yields. The observed products likely form from pyran intermediates that undergo an oxa-6π electrocyclic ring opening to a functionalized dienone, followed by ring closure with an accompanying acyl shift.
创建时间：
2016-05-05
