首页> 外文期刊>Tetrahedron letters: The International Journal for the Rapid Publication of Preliminary Communications in Organic Chemistry >Access to enantiopure polycyclic beta-lactams by Diels-Alder reaction of novel inner-outer-ring 2-(silyloxy)dienes with a carbacepham skeleton
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Access to enantiopure polycyclic beta-lactams by Diels-Alder reaction of novel inner-outer-ring 2-(silyloxy)dienes with a carbacepham skeleton

机译:新型内-外环2-(甲硅烷氧基)二烯与咔唑骨架的Diels-Alder反应获得对映纯多环β-内酰胺

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摘要

The synthesis of unprecedented inner-outer-ring 2-[tert-butyldimethylsilyloxy]dienes with a carbacepham structure in optically pure form and their totally pi-facial endo selective Diels-Alder reactions to structurally novel polycyclic P-lactams is reported.
机译:据报道,以纯净的形式合成了前所未有的具有咔巴庚结构的内外环2- [叔丁基二甲基甲硅烷氧基]二烯,以及它们对整个结构新颖的多环P-内酰胺的全部表面内选择性Diels-Alder反应。

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