A Tandem 1,3-H-Shift–6π-Electrocyclization–Cyclic 2-Amido-diene Intramolecular Diels–Alder Cycloaddition Approach to BCD-Ring of Atropurpuran
Organic Letters2011Vol. 14(1), pp. 252–255
Citations Over TimeTop 10% of 2011 papers
Abstract
An approach toward the BCD-ring of atropurpuran via a sequence of allenic 1,3-H shift, 6π-electron pericyclic ring closure, and intramolecular Diels-Alder cycloaddition of cyclic 2-amidodiene is described.
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