Total synthesis of (-)-nakadomarin A: alkyne ring-closing metathesis

A 13-step, highly stereoselective synthesis of (-)-nakadomarin A has been achieved using the combination of a bifunctional organocatalyst controlled Michael addition, a nitro-Mannich/lactamization cascade, an alkyne ring-closing metathesis/syn-reduction, and furan/iminium ion cyclization/reduction a...

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Bibliografski detalji
Glavni autori: Jakubec, P, Kyle, A, Calleja, J, Dixon, D
Format: Journal article
Jezik:English
Izdano: 2011