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首页> 外文期刊>Organic letters >Photochemical Rearrangement of Oxaziridines and Nitrones in the Hexahydroindole Series: A Convenient Synthetic Route to 1-Azabicyclo[5.2.0]nonan-2-ones as Novel GRD Mimetics
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Photochemical Rearrangement of Oxaziridines and Nitrones in the Hexahydroindole Series: A Convenient Synthetic Route to 1-Azabicyclo[5.2.0]nonan-2-ones as Novel GRD Mimetics

机译:六氢吲哚系列中的恶唑烷和硝基的光化学重排:合成新型GRD模拟物的1-Azabicyclo [5.2.0] nonan-2-one的简便合成路线

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摘要

Photolysis of oxaziridines a or nitrones b provides a convenient synthetic route to fused bicyclic lactams c adequately substituted on both cycles A and B as scaffolds for mimicking conformationally constrained β-turn peptides as in the tripeptide RGD signaling motif of fibronectin.
机译:恶唑烷酮a或硝酮b的光解提供了一条便利的合成路线,以合成在环A和B上都被取代的稠合双环内酰胺c,作为模拟纤连蛋白RGD信号转导基序的构象受限的β-turn肽的支架。

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