| 摘要 |
<p>The present invention provides a method for stereoselectively synthesizingβ-functionalized cyclic enone. Theβ-functionalized cyclic enone is stereoseletively synthesized by making non-functionalized cyclic enone react with diazoacetate in the presence of an oxazabororidium ion catalyst. According to the method,β-functionalized cyclic enone can be stereoselectively synthesized with high efficiency by a single step.</p> |
