Development of Bifunctional Chiral Thioureas and Thiosquaramides in the Synthesis of Betti Bases

双功能手性硫脲和硫代方酰胺在贝蒂碱合成中的应用

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Abstract

Bifunctional thioureas and, for the first time, bifunctional thiosquaramides as organocatalysts were used in the asymmetric Betti reaction involving 1-, 2-naphthols and hydroxyquinoline with N-tosylimine and ketimine. The described methodology affords direct access to chiral aminoarylnaphthols in excellent yield (up to 98%) with high enantioselectivity (up to 80% ee) and enantioenriched 3-amino-2-oxindoles (up to 78% yield, up to 98% ee).

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