立体中心
分子内力
芯(光纤)
催化作用
化学
四级碳
配体(生物化学)
中心(范畴论)
组合化学
立体化学
对映选择合成
计算机科学
有机化学
结晶学
受体
电信
生物化学
作者
Yankun Zhao,Hongya Yan,Yulian Zhang,Tao Zhou,Mengxing Tian,Chongzhou Zhang,Shan Yuan,Han‐Yue Qiu,Ling He,Min Zhang
出处
期刊:Chemical Science
[Royal Society of Chemistry]
日期:2024-01-01
卷期号:15 (28): 10963-10968
被引量:4
摘要
The catalytic asymmetric propargylation of enol(ate) intermediates is a well-established method for the synthesis of α-propargyl-substituted carbonyl compounds. However, the propargylation of homo-enol(ate) or its equivalents for the synthesis of β-propargyl-substituted carbonyl compounds remains underdeveloped. A catalytic enantioselective decarboxylative intramolecular propargylation of cyclopropanols has been developed using a PyBox-complexed copper catalyst. This reaction offers an effective approach to assemble a cyclopentanone skeleton bearing an all-carbon quaternary stereogenic center and an adjacent quaternary gem-dimethyl carbon center, which is the core scaffold of the naturally occurring cuparenoids. Key to the success of this protocol is the use of a new structurally optimized PyBox ligand. This study represents the first example of catalytic asymmetric intramolecular propargylation of cyclopropanols.
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