首页> 外文期刊>The Journal of Organic Chemistry >Novel Synthons from Mucochloric Acid: The First Use of α,β-Dichloro-γ-butenolides and γ-Butyrolactams for Direct Vinylogous Aldol Addition
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Novel Synthons from Mucochloric Acid: The First Use of α,β-Dichloro-γ-butenolides and γ-Butyrolactams for Direct Vinylogous Aldol Addition

机译:来自粘氯酸的新型合成子:α,β-二氯-γ-丁烯内酯和γ-丁内酰胺首次用于直接葡萄酒醛缩醛加成

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摘要

Novel 5-(1′-hydroxy)-γ-butyrolactone and γ-butyrolactam subunits were synthesized by direct vinylogous aldol addition of α,β-dichloro γ-butyrolactones and γ-butyrolactams with aldehydes under basic conditions. Different bases and solvents were screened in the context of generating γ-butyrolactones. Diastereo-selectivity was observed and γ-butenolides and γ-butyrolactams showed opposite diastereoselectivity under the same reaction condition.
机译:在碱性条件下,通过醛基直接将α,β-二氯γ-丁内酯和γ-丁内酰胺与乙烯醛乙烯基醇醛加成,合成了新型的5-(1'-羟基)-γ-丁内酯和γ-丁内酰胺亚基。在生成γ-丁内酯的背景下筛选了不同的碱和溶剂。在相同的反应条件下,观察到非对映选择性,并且γ-丁烯内酯和γ-丁内酰胺显示相反的非对映选择性。

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