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A stannous chloride-induced deacetalisation-cyclisation process to prepare the ABC ring system of 'upenamide

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JournalTetrahedron Letters
DatePublished - 17 May 2004
Issue number21
Volume45
Number of pages3
Pages (from-to)4181-4183
Original languageEnglish

Abstract

A stannous chloride-induced deacetalisation-cyclisation approach to the ABC core of the macrocyclic alkaloid, 'upenamide is reported. The use of a substituted beta-lactone to prepare a C-2 substituted 'upenamide analogue is also disclosed. (C) 2004 Elsevier Ltd. All rights reserved.

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  • MARINE SPONGE

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