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首页> 外文期刊>ACS catalysis >Highly Enantioselective Synthesis of Dihydroquinazolinones Catalyzed by SPINOL-Phosphoric Acids
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Highly Enantioselective Synthesis of Dihydroquinazolinones Catalyzed by SPINOL-Phosphoric Acids

机译:SPINOL-磷酸催化高对映选择性合成二氢喹唑啉酮

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摘要

The asymmetric condensation/amine addition cascade sequence of 2-aminobenzamides and aldehydes catalyzed by chiral spirocyclic SPINOL-phosphoric acids was realized. SPINOL-phosphoric acid 1j was found to be a general, highly enantioselective organocatalyst for such cascade reactions at room temperature, affording 2,3-dihydroquinazolinones in excellent yields (up to 99%) with good to excellent ee’s (up to 98%). The best level of stereocontrol was obtained for aromatic aldehydes with an ortho substituent.
机译:实现了手性螺环SPINOL-磷酸催化2-氨基苯甲酰胺和醛的不对称缩合/胺加成级联序列。发现SPINOL-磷酸1j是在室温下进行此类级联反应的通用,高对映选择性的有机催化剂,能够以优异的收率(高达99%)和良好的ee(高达98%)提供2,3-二氢喹唑啉酮。对于具有邻位取代基的芳族醛,可获得最佳的立体控制水平。

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