摘要
报道了一种钯催化三取代烯烃的不对称分子间氢羧基化反应,以中等到优秀的产率、对映选择性以及优异的非对映选择性得到了一系列含有两个手性中心的琥珀酸衍生物.所得手性丁二酸酯类化合物通过简单的衍生化即可制备高光学纯度的γ-丁内酯类化合物,彰显了该催化方法在有机合成中的潜在应用.
A palladium-catalyzed asymmetric intermolecular hydrocarboxylation of trisubstituted alkenes was reported,which afforded a series of succinic acid derivatives containing two chiral centers with moderate to excellent yields,enantioselectivity,and high diastereoselectivity.The resulting dimethyl succinates can be easily converted to optically activeγ-butyrolactones,demonstrating the potential application of this method.
作者
王震
董开武
Wang Zhen;Dong Kaiwu(Shanghai Key Laboratory of Green Chemistry and Chemical Processes,Chang-Kung Chuang Institute,School of Chemistry and Molecular Engineering,East China Normal University,Shanghai 200062)
出处
《有机化学》
SCIE
CAS
CSCD
北大核心
2024年第10期3249-3257,共9页
Chinese Journal of Organic Chemistry
基金
国家自然科学基金(No.22271094)资助项目.
关键词
钯
不对称
氢羰基化
烯烃
琥珀酸
一氧化碳
palladium
asymmetric
hydrocarbonylation
alkene
succinic acid
carbon monoxide