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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 of 3-aryl-3,4-dihydroisocoumarins by regioselective domino '[3+3] cyclization/lactonization' reactions of 1,3-bis-(silyloxy)-1,3-butadienes with 1 -hydroxy-5-silyloxy-4-en-3-ones
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Synthesis of 3-aryl-3,4-dihydroisocoumarins by regioselective domino '[3+3] cyclization/lactonization' reactions of 1,3-bis-(silyloxy)-1,3-butadienes with 1 -hydroxy-5-silyloxy-4-en-3-ones

机译:1,3-双-(甲硅烷氧基)-1,3-丁二烯与1-羟基-5-甲硅烷氧基-的区域选择性多米诺“ [3 + 3]环化/内酯化”反应合成3-芳基-3,4-二氢异香豆素4-en-3-ones

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摘要

The [3+3] cyclization of 1,3-bis(silyloxy)-1,3-butadienes with 1-hydroxy-5-silyloxy-4-en-3-ones afforded 6-(2-aryl-2-chloroethyl)salicylates, which were transformed into 3-aryl-3,4-dihydroisocoumarins by silica gel-mediated lactonization.
机译:1,3-双(甲硅烷氧基)-1,3-丁二烯与1-羟基-5-甲硅烷氧基-4-烯-3-酮的[3 + 3]环化反应得到6-(2-芳基-2-氯乙基)水杨酸酯,通过硅胶介导的内酯化将其转化为3-芳基-3,4-二氢异香豆素。

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