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首页> 外文期刊>Tetrahedron letters: The International Journal for the Rapid Publication of Preliminary Communications in Organic Chemistry >Synthesis and reactions of hydroxyspiro[5.2]cyclooctenones based on the cyclization of the dianions of acetone and diethyl 2-oxopropylphosphonate with 1,1-diacylcyclopropanes
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Synthesis and reactions of hydroxyspiro[5.2]cyclooctenones based on the cyclization of the dianions of acetone and diethyl 2-oxopropylphosphonate with 1,1-diacylcyclopropanes

机译:基于丙酮和2-氧丙基丙基二膦酸二乙酯与1,1-二酰基环丙烷的环化反应,羟基螺[5.2]环辛烯酮的合成和反应

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摘要

The cyclization of the dianions of diethyl 2-oxopropylphosphonate and of acetone with 1,1-diacylopropanes afforded hydroxy-spiro[5.2]cyclooctenones which were transformed,by homo-Michael reactions with tetrabutylammonium halides,into various function-alized phenols or their dimers.
机译:将2-氧丙基丙基膦酸二乙酯和丙酮的二价阴离子与1,1-二酰基丙烷环合,得到羟基-螺[5.2]环辛烯酮,通过与四丁基卤化铵的均一迈克尔反应,转化为各种官能化的酚或其二聚体。

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