对映体药物
化学
立体中心
废止
吲哚
对映体
分子内力
催化作用
亚砜
对映选择合成
表面改性
组合化学
立体化学
有机化学
物理化学
作者
Somratan Sau,Kallol Mukherjee,Koneti Kondalarao,Vincent Gandon,Akhila K. Sahoo
出处
期刊:Organic Letters
[American Chemical Society]
日期:2023-10-16
卷期号:25 (42): 7667-7672
被引量:11
标识
DOI:10.1021/acs.orglett.3c02969
摘要
Developed herein is a chiral sulfoximine-enabled Ru(II)-catalyzed asymmetric C-H activation/functionalization involving intramolecular hydroarylation and functionalization/annulation of alkynes. This process constructs dihydrobenzofuran- or indoline-fused isoquinolinones having a tertiary or quaternary stereocenter with good yields and enantioselectivities (up to 97:3 enantiomeric ratio). The chiral sulfoxide precursor used in synthesizing the enantiopure sulfoximines is spontaneously eliminated during the reaction. It can be recovered without losing enantiopurity (∼99% enantiomeric excess) and reused.
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