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Asymmetric Mukaiyama aldol reaction of silyl enol ethers with aldehydes using a polymer-supported chiral Lewis acid catalyst

机译:聚合物负载的手性路易斯酸催化剂对甲硅烷基烯醇醚与醛的不对称向海山醇醛反应

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摘要

Chiral N-sulfonylated a-amino acid monomer (5) derived from (S)-tryptophan was copolymerized with styrene and divinylbenzene under radical polymerization conditions to give a polymer-supported N-sulfonyl-(S)-tryptophan (6). Treatment of the polymer-supported chiral ligand with 3,5-bis(trifluoromethyl)phenyl boron dichloride afforded a polymeric Lewis acid catalyst (16) effective for asymmetric Mukaiyama aldol reaction of silyl enol ethers and aldehydes. Various aldehydes were allowed to react with silyl enol ethers in the presence of the polymeric chiral Lewis acid to give the corresponding aldol adducts in high yield with high levels of enantioselectivity. (c) 2005 Elsevier Ltd. All rights reserved.
机译:在自由基聚合条件下,将衍生自(S)-色氨酸的手性N-磺酰化α-氨基酸单体(5)与苯乙烯和二乙烯基苯共聚,得到聚合物负载的N-磺酰基-(S)-色氨酸(6)。用3,5-双(三氟甲基)苯基二氯化硼处理聚合物负载的手性配体,得到聚合物路易斯酸催化剂(16),其对于甲硅烷基烯醇醚和醛的不对称Mukaiyama aldol反应有效。在聚合手性路易斯酸的存在下,使各种醛与甲硅烷基烯醇醚反应,以高收率和高对映体选择性得到相应的羟醛加合物。 (c)2005 Elsevier Ltd.保留所有权利。

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