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引用次数: 0

摘要

芳香醛的-烷基烯丙酸酯得到4 H -1,3-二氧辛-6-基丙酸14,具有优异的非对映选择性。机理研究表明,这些复杂杂环是由α -和γ -位置上连续的Morita-Baylis-Hillman反应、缩化反应和最终的分子内oxa-Michael反应组成的四步反应级联反应的结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A
-alkyl allenoate esters aromatic aldehydes to give 4 H -1,3-di-oxin-6-yl-propanoates 14 with excellent diastereoselectivity. Mech- anistic studies revealed that these complex heterocycles are obtained as a result of a four-step reaction cascade consisting of two consec-utive Morita–Baylis–Hillman reactions on the α - and γ -position, an acetalization, and a final ring-closing intramolecular oxa-Michael reaction.
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