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Development of Phase-Transfer-CatalyzedAsymmetric Strecker Reaction Basedon the Molecular Design of Chiral QuaternaryAmmonium Salts

机译:基于手性季铵盐的分子设计的相转移催化不对称反应的发展

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Asymmetric Strecker reaction of aldimines using aqueouspotassium cyanide (KCN) as a cyanide source has beendevised through the molecular design of chiral phase-transfercatalyst 9 bearing a stereochemically defined tetranaphthylbackbone. Further, highly efficient, enantioselective synthesisof N-protected a-amino nitriles from the corresponding a-amido sulfones under similar biphasic conditions is alsodescribed, featuring its practical advantages.
机译:使用氰化钾(KCN)作为氰化物源的非对称斑块反应,作为氰化物源,致力于载有立体化学定义的四萘啶酮的手性相转移催化剂9的分子设计。此外,在相似的双相条件下,高效高效地,来自相应的A-氨基砜的N保护的A-氨基腈的致力化合成是Alsodscribed,具有其实际优点。

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