跳转至内容
Merck
CN
  • Attempts to improve the overall stereoselectivity of the Ireland-Claisen rearrangement.

Attempts to improve the overall stereoselectivity of the Ireland-Claisen rearrangement.

Organic letters (2009-01-09)
Chi-Li Chen, Kosuke Namba, Yoshito Kishi
摘要

With focus on the steric effects present in the transition states for the [3,3]-sigmatropic rearrangement, the substrate 5 has been designed to improve the overall stereoselectivity of the Ireland-Claisen rearrangement. Experimentally, it has been found that (1) only Z-6 rearranges to 7 at 80 degrees C and (2) E-6 isomerizes to Z-6 at 80 degrees C, thereby allowing the transformation of 5 into 7 in an almost quantitative yield. To illustrate the usefulness of this approach, two additional examples are given.