Structure and stereochemistry of an anti-inflammatory anhydrosugar from the Australian marine sponge Plakinastrella clathrata and the synthesis of two analogues-Reference-Cited by-同舟云学术

Structure and stereochemistry of an anti-inflammatory anhydrosugar from the Australian marine sponge Plakinastrella clathrata and the synthesis of two analogues

Published:2013-09 Issue:37 Volume:69 Page:8074-8079
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Katavic Peter L.,Yong Ken W.L.,Herring Joel N.,Deseo Myrna A.,Blanchfield Joanne T.,Ferro Vito,Garson Mary J.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference14 articles.

1. Glycolipids from Sponges. 6.1 Plakoside A and B, Two Unique Prenylated Glycosphingolipids with Immunosuppressive Activity from the Marine Sponge Plakortis simplex

2. Glycolipids from Sponges. 11. Isocrasserides, Novel Glycolipids with a Five-Membered Cyclitol Widely Distributed in Marine Sponges

3. Configurational Assignment of Cyclic Peroxy Metabolites Provides an Insight into Their Biosynthesis: Isolation of Plakortolides, seco-Plakortolides, and Plakortones from the Australian Marine Sponge Plakinastrella clathrata

4. Oxidative Processes in the Australian Marine Sponge Plakinastrella clathrata: Isolation of Plakortolides with Oxidatively Modified Side Chains

5. Plakortolide Stereochemistry Revisited: The Checkered History of Plakortolides E and I

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