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A general synthesis of the acarnidines
Authors:John W Blunt  Murray HG Munro  Selwyn C Yorke
Institution:Chemistry Department, University of Canterbury, Christchurch, New Zealand
Abstract:A general synthetic route to the biologically active marine natural products, the acarnidines (10a–c),1 and bolecules of the acarnidine type, is presented. The substituted homospermidine skeleton of the acarnidines was synthesised via an aldimine intermediate prepared from mono-BOC protected 1,5-diaminopentane (5) and the aldehyde (4).
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