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Asymmetric Henry reaction catalyzed by chiral Cu(II) salalen and salan complexes derived from (S)-proline

机译:由手性铜(II)催化的不对称亨利反应均唾液和盐酸盐络合物衍生自-Proline

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摘要

Single chiral center C-1 symmetric salalen and salan ligands were synthesized from (S)-proline and their Cu(II) complexes were used as catalysts for the asymmetric Henry reaction between aromatic aldehydes and nitromethane/nitroethane. The reaction of 4-nitrobenzaldehyde and nitromethane using salalen ligand (10 mol%) and Cu(OAc)(2) .H(2)0 (10 mol%) in isopropanol with 4-methoxyphenol (10 mol%) as an additive at room temperature, afforded the (S)-2-nitro-l-(4-nitrophenyl)ethanol in 82% yield and 81% ee. We have also generalized the catalysis of nitro-aldol reaction for a variety of substrates using nitromethane, gave 67-94% yields with 49-98% ee after 96-120 h. The absolute configuration of nitro-aldol product was governed by the use of the metal, Mn(III) complex of the ligand 2 gives (R)-enantiomer while Cu(II) complex of same ligand gives the (S)-enantiomer. (C) 2018 Elsevier B.V. All rights reserved.
机译:从(S) - 脯氨酸中合成单手性中心C-1对称的Salalen和Salan配体,用它们的Cu(II)配合物用作芳香族醛和硝基甲烷/硝基乙烷之间的不对称亨利反应的催化剂。 用4-甲氧基苯酚(10mol%)作为添加剂,使用Salalen配体(10mol%)和硝基甲烷(10mol%)和Cu(2).h(2).h(2)0(10mol%)作为添加剂的异丙醇(10mol%)的反应。 室温,得到(S)-2-硝基-1-(4-硝基苯基)乙醇,82%收率和81%EE。 我们还在使用硝基甲烷的各种基材的催化剂上推出了硝基-Aldol反应的催化,得到67-94%的产率,96-120小时后49-98%EE。 硝基-Aldol产物的绝对构型通过使用配体2的金属,Mn(III)络合物来控制(R) - 蒽料,而同一配体的Cu(II)复合物给予(S) - 蒽酸甲酯。 (c)2018年elestvier b.v.保留所有权利。

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