Abstract
We report herein full details of the first example of a Cope rearrangement in which the C3-C4 bond of the β-lactam nucleus is the central bond of the 1,5-hexadiene system, thus providing an easy and efficient entry to novel, and in some cases optically pure functionalized azocinones.
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Almendros, P., Aragoncillo, C., Cabrero, G., Callejo, R., Carrascosa, R., Luna, A., … Ruizb, M. P. (2010). Thermal Cope reaction of 2-azetidinone-tethered 1,5-dienes: Synthesis of tetrahydroazocinones. Arkivoc, 2010(3), 74–92. https://doi.org/10.3998/ark.5550190.0011.308
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