首页> 外文期刊>Tetrahedron letters: The International Journal for the Rapid Publication of Preliminary Communications in Organic Chemistry >Stereoselective synthesis of tetrahydro-2H-[2]benzopyrano[3,4-c]pyrrol-3-ones and related compounds as precursors of serotonin 5-HT_(2C) receptor agonists
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Stereoselective synthesis of tetrahydro-2H-[2]benzopyrano[3,4-c]pyrrol-3-ones and related compounds as precursors of serotonin 5-HT_(2C) receptor agonists

机译:立体选择性合成四氢-2H- [2]苯并吡喃并[3,4-c]吡咯-3-酮和相关化合物作为5-羟色胺5-HT_(2C)受体激动剂的前体

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摘要

Tetrahydro-2H-[2]benzopyrano[3,4-c]pyrroI-3-ones and the related 3a-methyl-2,3.3a,4,5,9b-hexahydro-1H-benzo[e]isoindole analogues were synthesised by an intramolecular Diels-Alder reaction. The observed stereoselectivity was dependent upon the nature of the tethered dienophile as well as the judicious placement of the amide.
机译:合成了四氢-2H- [2]苯并吡喃并[3,4-c]吡咯I-3-酮和相关的3a-甲基-2,3.3a,4,5,9b-六氢-1H-苯并[e]异吲哚类似物通过分子内Diels-Alder反应。观察到的立体选择性取决于束缚的双亲物的性质以及酰胺的明智位置。

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