首页> 外文期刊>Journal of Heterocyclic Chemistry: The International Journal of Heterocyclic Chemistry >MICHAEL ADDITION OF BENZOYLACETONITRILE TO CHIRAL ALPHA-CYANOACRYLATES DERIVED FROM ENANTIOMERICALLY PURE ALPHA-HYDROXYALDEHYDES - SYNTHESIS OF 3-ALKOXYCARBONYL-4-ALKYL-2-AMINO-5-CYANO-6-PHENYL-4H-PYRAN
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MICHAEL ADDITION OF BENZOYLACETONITRILE TO CHIRAL ALPHA-CYANOACRYLATES DERIVED FROM ENANTIOMERICALLY PURE ALPHA-HYDROXYALDEHYDES - SYNTHESIS OF 3-ALKOXYCARBONYL-4-ALKYL-2-AMINO-5-CYANO-6-PHENYL-4H-PYRAN

机译:苯甲酰基乙腈与对映体纯的羟基缩醛衍生的手性α-氰基丙烯酸酯的加成反应-合成3-烷氧基羰基-4-烷基-2-氨基-2-氰基-5-氰基-6-苯基-4H-吡喃

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摘要

We describe the Michael addition of benzoylacetonitrile to alpha-cyanoacrylates 4a-c and 5a obtained from readily available chiral alpha-hydroxyaldehydes 1a-c. The resulting polyfunctionalized 4-alkyl-2-amino-4H-pyrans 6a-c, 7a have been obtained in good yield and moderate diastereoselectivity. [References: 13]
机译:我们描述了从容易获得的手性α-羟基醛1a-c获得的α-氰基丙烯酸酯4a-c和5a的苯甲酰基乙腈的迈克尔加成。已经以良好的产率和中等的非对映选择性获得了所得的多官能化的4-烷基-2-氨基-4H-吡喃6a-c,7a。 [参考:13]

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