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Asymmetric One-Pot Synthesis of 1,3-Oxazolidines and 1,3?Oxazinanes via Hemiaminal Intermediates

机译:Hemiaminal中间体不对称一锅合成1,3-恶唑烷和1,3?恶嗪酮

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摘要

A highly efficient method for the enantioselective one-pot synthesis of 1,3-oxazolidines and 1,3-oxazinanes has been reported. The reaction proceeds via the formation of hemiaminal intermediates obtained by the enantioselective addition of respective alcohols to imines catalyzed by a chiral magnesium phosphate catalyst, followed by intramolecular cyclization under mildly basic conditions. A wide range of substrates have been converted to the respective chiral heterocyclic products in high yields and with excellent enantioselectivities using this one-pot procedure.
机译:已经报道了一种高效的1,3-恶唑烷和1,3-恶嗪酮的对映选择性一锅合成方法。该反应通过形成通过将相应的醇对映选择性地加成至手性磷酸镁催化剂催化的亚胺而获得的半胱氨酸中间体进行,然后在温和的碱性条件下进行分子内环化。使用这种一锅法,各种各样的底物已经以高收率和优异的对映选择性被转化为各自的手性杂环产物。

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