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首页> 外文期刊>Advanced synthesis & catalysis >Phosphine-Catalyzed Asymmetric [4+2] Annulation of Vinyl Ketones with Oxindole-Derived α,β-Unsaturated Imines: Enantioselective Syntheses of 2',3'-Dihydro-1'H-spiro[indoline-3,4'-pyridin] -2-ones
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Phosphine-Catalyzed Asymmetric [4+2] Annulation of Vinyl Ketones with Oxindole-Derived α,β-Unsaturated Imines: Enantioselective Syntheses of 2',3'-Dihydro-1'H-spiro[indoline-3,4'-pyridin] -2-ones

机译:膦催化的含氧吲哚衍生的α,β-不饱和亚胺的乙烯基酮的不对称[4 + 2]环状:2',3'-Dihydro-1'H-spiro [indoline-3,4'-pyridin]的对映选择性合成-2-一

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摘要

A novel asymmetric [4+2] annulation of vinyl ketones with oxindole-derived α,β-unsaturated imines has been developed in the presence of a multifunctional thiourea-phosphine catalyst derived from a natural amino acid, providing the first phos-phine-catalyzed enantioselective synthesis of 2',3'-dihydro-1'H-spiro[indoline-3,4'-pyridin]-2-ones in good yields with excellent stereoselectivities under mild conditions.
机译:在衍生自天然氨基酸的多功能硫脲-膦催化剂的存在下,开发了一种新型的不对称的[4 + 2]乙烯基酮与羟吲哚衍生的α,β-不饱和亚胺环合的方法,该方法提供了首个被膦膦催化的化合物在温和条件下以良好的收率和良好的立体选择性对映体选择性合成2',3'-dihydro-1'H-spiro [indoline-3,4'-pyridin] -2-one。

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