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

M  Reid; R J K  Taylor

doi:10.1016/j.tetlet.2004.03.119

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

M Reid, R J K Taylor

Chemistry

Research output: Contribution to journal › Article › peer-review

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.

Original language	English
Pages (from-to)	4181-4183
Number of pages	3
Journal	Tetrahedron Letters
Volume	45
Issue number	21
DOIs	https://doi.org/10.1016/j.tetlet.2004.03.119
Publication status	Published - 17 May 2004

Keywords

MARINE SPONGE

Access to Document

10.1016/j.tetlet.2004.03.119

Cite this

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

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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AB - 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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U2 - 10.1016/j.tetlet.2004.03.119

DO - 10.1016/j.tetlet.2004.03.119

M3 - Article

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