Synthesis of sub-units of marine polycyclic ethers by ring-closing metathesis and hydroboration of enol ethers
作者:J. Stephen Clark、Jason G. Kettle
DOI:10.1016/s0040-4020(99)00303-8
日期:1999.7
The construction of polycyclic ethers by sequential ring-closing metathesis and stereoselective hydroboration of enol ethers has been explored. This reaction sequence has been used to prepare bicyclic ethers corresponding to sub-units found in the brevetoxins and related marine natural products.
已经探索了通过连续的闭环易位和烯醇醚的立体选择性氢硼化来构建多环醚。该反应序列已用于制备与在短毒素和相关海洋天然产物中发现的亚单位相对应的双环醚。