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Relative and absolute stereochemistry of diacarperoxides: antimalarial norditerpene endoperoxides fr...

Relative and absolute stereochemistry of diacarperoxides: antimalarial norditerpene endoperoxides fr...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_3bfccd1f58e14c46bf9cdbbb521966cb

Relative and absolute stereochemistry of diacarperoxides: antimalarial norditerpene endoperoxides from marine sponge Diacarnus megaspinorhabdosa

About this item

Full title

Relative and absolute stereochemistry of diacarperoxides: antimalarial norditerpene endoperoxides from marine sponge Diacarnus megaspinorhabdosa

Publisher

Switzerland: MDPI AG

Journal title

Marine drugs, 2014-08, Vol.12 (8), p.4399-4416

Language

English

Formats

Publication information

Publisher

Switzerland: MDPI AG

More information

Scope and Contents

Contents

Five new norditerpene endoperoxides, named diacarperoxides H-L (1-5), and a new norditerpene diol, called diacardiol B (6), were isolated from the South China Sea sponge, Diacarnus megaspinorhabdosa. Their structures, including conformations and absolute configurations, were determined by using spectroscopic analyses, computational approaches and c...

Alternative Titles

Full title

Relative and absolute stereochemistry of diacarperoxides: antimalarial norditerpene endoperoxides from marine sponge Diacarnus megaspinorhabdosa

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_doaj_primary_oai_doaj_org_article_3bfccd1f58e14c46bf9cdbbb521966cb

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_3bfccd1f58e14c46bf9cdbbb521966cb

Other Identifiers

ISSN

1660-3397

E-ISSN

1660-3397

DOI

10.3390/md12084399

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