<?xml version="1.0"?>
<oai_dc:dc xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
  <dc:title>Benzosceptrins A and B with a unique benzocyclobutane skeleton and nagelamide S and T from Pacific sponges</dc:title>
  <dc:creator>Appenzeller, J.</dc:creator>
  <dc:creator>Tilvi, S.</dc:creator>
  <dc:creator>Martin, M. T.</dc:creator>
  <dc:creator>Gallard, J. F.</dc:creator>
  <dc:creator>El-bitar, H.</dc:creator>
  <dc:creator>Dau, E. T. H.</dc:creator>
  <dc:creator>/Debitus, C&#xE9;cile</dc:creator>
  <dc:creator>/Laurent, Dominique</dc:creator>
  <dc:creator>Moriou, C.</dc:creator>
  <dc:creator>Al-Mourabit, A.</dc:creator>
  <dc:description>Four new dimeric pyrrole-2-aminoimidazole alkaloids have been isolated from the Pacific marine sponges Agelas cf. mauritiana and Phakellia sp. They include the unusual C2 symmetrical benzosceptrins A (4) and B (5), which each possess a unique benzocyclobutane skeleton and nagelamides S (6) and T (7). Their structures and relative configuration were elucidated from spectroscopic data. Plausible biogenetic paths for these compounds are also proposed in this paper.</dc:description>
  <dc:date>2009</dc:date>
  <dc:type>text</dc:type>
  <dc:identifier>https://www.documentation.ird.fr/hor/fdi:010090950</dc:identifier>
  <dc:identifier>fdi:010090950</dc:identifier>
  <dc:identifier>Appenzeller J., Tilvi S., Martin M. T., Gallard J. F., El-bitar H., Dau E. T. H., Debitus C&#xE9;cile, Laurent Dominique, Moriou C., Al-Mourabit A.. Benzosceptrins A and B with a unique benzocyclobutane skeleton and nagelamide S and T from Pacific sponges. 2009, 11 (21),  4874-4877</dc:identifier>
  <dc:language>EN</dc:language>
</oai_dc:dc>
