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Asymmetric synthesis of α-aminophosphonates by means of direct organocatalytic three-component hydrophosphonylation

Asymmetric synthesis of α-aminophosphonates by means of direct organocatalytic three-component hydrophosphonylation
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摘要 The direct asymmetric three-component reaction of an aromatic (or cinnamic) aldehyde, an amine and a phosphite was investigated by employing chiral BrΦnsted acid. In general, modest to good enantioselectivities (31%–87% ee) could be obtained in acceptable isolated yields (61%–91%) for a series of substrates. The direct asymmetric three-component reaction of an aromatic (or cinnamic) aldehyde, an amine and a phosphite was investigated by employing chiral BrФnsted acid. In general, modest to good enantioselectivities (31%-87% ee) could be obtained in acceptable isolated yields (61%-91%) for a series of substrates.
出处 《Chinese Science Bulletin》 SCIE EI CAS 2010年第17期1729-1731,共3页
基金 supported by the National Natural Science Foundation of China (20772091) Tianjin Municipal Science and Technology Commis-sion (07JCZDJC04700)
关键词 不对称合成 Α-氨基膦酸酯 三组分 有机催化 对映选择性 亚磷酸酯 手性 Ф-aminophosphonate, organocatalysis, aromatic aldehyde, three-component reaction, enantioselectivity
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