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首页> 外文期刊>Tetrahedron >A NEW METHOD FOR PREPARATION OF 3,6-DIHYDRO-2H-1,3-OXAZINES AND EXPLORATIONS OF THEIR USE IN STEREOSELECTIVE SYNTHESIS OF 1,3-AMINO ALCOHOL DERIVATIVES
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A NEW METHOD FOR PREPARATION OF 3,6-DIHYDRO-2H-1,3-OXAZINES AND EXPLORATIONS OF THEIR USE IN STEREOSELECTIVE SYNTHESIS OF 1,3-AMINO ALCOHOL DERIVATIVES

机译:制备3,6-二氢-2H-1,3-恶嗪的新方法及其在立体选择性合成1,3-氨基醇衍生物中的用途的探索

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摘要

Condensation of P-hydroxy aldehydes with N-sulfonyl aldimines produces 3,6-dihydro-2H-1,3-oxazines in moderate to excellent yields. The process is stereoselective, with the C-2 and C-6 substituents having a trans relationship in these heterocycles. Some transformations of these oxazines as potential acyclic 1,3-amino alcohol synthons are described. [References: 30]
机译:P-羟基醛与N-磺酰基醛亚胺的缩合以中等至优异的产率产生3,6-二氢-2H-1,3-恶嗪。该方法是立体选择性的,在这些杂环中C-2和C-6取代基具有反式关系。描述了这些恶嗪作为潜在的无环1,3-氨基醇合成子的一些转化。 [参考:30]

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