Synthesis of 3-hydroxyindolin-2-one alkaloids, (±)-donaxaridine and (±)-convolutamydines A and E, through enolization–Claisen rearrangement of 2-allyloxyindolin-3-ones-Reference-Cited by-同舟云学术

Synthesis of 3-hydroxyindolin-2-one alkaloids, (±)-donaxaridine and (±)-convolutamydines A and E, through enolization–Claisen rearrangement of 2-allyloxyindolin-3-ones

Published:2004-04 Issue:15 Volume:60 Page:3493-3503
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Kawasaki Tomomi,Nagaoka Miyuki,Satoh Tomoko,Okamoto Ayako,Ukon Rie,Ogawa Atsuyo

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference67 articles.

1. Total Synthesis of Donaxaridine

2. Convolutamydine A, a novel bioactive hydroxyoxindole alkaloid from marine bryozoan Amathia convoluta

3. Isolation and structure of convolutamydines B ∼ D from marine bryozoan Amathia convoluta

4. Three New Alkaloids, Convolutamines F and G, and Convolutamydine E, from the Floridian Marine Bryozoan Amathia convoluta

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