Asymmetric synthesis of seven-carbon segments of the phorboxazoles and (−)-discodermolide: Complementary route from racemic trans-2,4-dimethyl-8-oxabicyclo[3.2.1]oct-6-en-3-one-Reference-Cited by-同舟云学术

Asymmetric synthesis of seven-carbon segments of the phorboxazoles and (−)-discodermolide: Complementary route from racemic trans-2,4-dimethyl-8-oxabicyclo[3.2.1]oct-6-en-3-one

Published:1999-04 Issue:14 Volume:55 Page:4315-4324
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Misske Andrea M,Hoffmann H.M.R

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference46 articles.

1. Phorboxazoles A and B: potent cytostatic macrolides from marine sponge Phorbas species

2. Absolute Configuration of Phorboxazoles A and B from the Marine Sponge Phorbas sp. 1. Macrolide and Hemiketal Rings

3. Absolute configuration of phorboxazoles A and B from the marine sponge, Phorbas sp. 2. C43 and complete stereochemistry

4. Discodermolide: a new bioactive polyhydroxylated lactone from the marine sponge Discodermia dissoluta

5. Discodermolide: a new bioactive polyhydroxylated lactone from the marine sponge Discodermia dissoluta [Erratum to document cited in CA113(9):75187b]

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