作者:Tadakatsu Mandai、Kengo Nishikawa、Hirofumi Yamaguchi、Mikio Kawada、Junzo Otera
DOI:10.1246/cl.1981.473
日期:1981.4.5
A sequence of allylation, the Wacker reaction, and desulfonylation of homoallyl sulfones provided a new synthetic method for the α,β,γ,δ-unsaturated ketone system often encountered in natural products. This procedure was successfully applied to ionone and irone synthesis.
高烯丙基砜的一系列烯丙基化、瓦克反应和脱磺酰化为天然产物中经常遇到的α,β,γ,δ-不饱和酮体系提供了一种新的合成方法。该程序成功应用于紫罗兰酮和铁的合成。