4.4 Article

Spirocyclization strategy toward indole phytoalexins. The first synthesis of (±)-1-methoxyspirobrassinin, (±)-1-methoxyspirobrassinol, and (±)-1-methoxyspirobrassinol methyl ether

Journal

TETRAHEDRON LETTERS
Volume 43, Issue 52, Pages 9489-9492

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/S0040-4039(02)02452-8

Keywords

phytoalexins; indoles; dioxane dibromide; spirocyclization; antitumor activity

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The first syntheses of cruciferous indole phytoalexins (+/-)-1-methoxyspirobrassinin, (+/-)-1-methoxyspirobrassinol, (+/-)-1-methoxyspirobrassinol methyl ether as well as a new syntheses of phytoalexins (+/-)-spirobrassinin and cyclobrassinin were achieved by dioxane dibromide (DDB)-mediated spirocyclization of brassinin and its I-substituted derivatives. (C) 2002 Elsevier Science Ltd. All rights reserved.

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