<?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>Marine natural occurring 2,5-diketopiperazines : isolation, synthesis and optical properties</dc:title>
  <dc:creator>Laville, R.</dc:creator>
  <dc:creator>Thanh Binh Nguyen</dc:creator>
  <dc:creator>Moriou, C.</dc:creator>
  <dc:creator>/Petek, Sylvain</dc:creator>
  <dc:creator>/Debitus, C&#xE9;cile</dc:creator>
  <dc:creator>Al-Mourabit, A.</dc:creator>
  <dc:subject>SUBSTANCE NATURELLE</dc:subject>
  <dc:subject>RECIF CORALLIEN</dc:subject>
  <dc:subject>INVERTEBRE AQUATIQUE</dc:subject>
  <dc:subject>EXTRACTION</dc:subject>
  <dc:subject>ANALYSE CHIMIQUE</dc:subject>
  <dc:subject>STRUCTURE CHIMIQUE</dc:subject>
  <dc:subject>SPECTROSCOPIE</dc:subject>
  <dc:subject>EPONGE MARINE</dc:subject>
  <dc:description>Seven 2,5-diketopiperazines (DKPs) were isolated from the Fijian marine sponge Acanthella cavernosa. NMR and circular dichroism (CD) comparison with synthetic L-L DKPs allowed us to determine unambiguously the L-L absolute configuration of the natural DKPs. This work initiated the setting up of an optical properties database of natural DKPs, including specific rotation and CD.</dc:description>
  <dc:date>2015</dc:date>
  <dc:type>text</dc:type>
  <dc:identifier>https://www.documentation.ird.fr/hor/fdi:010063520</dc:identifier>
  <dc:identifier>fdi:010063520</dc:identifier>
  <dc:identifier>Laville R., Thanh Binh Nguyen, Moriou C., Petek Sylvain, Debitus C&#xE9;cile, Al-Mourabit A.. Marine natural occurring 2,5-diketopiperazines : isolation, synthesis and optical properties. 2015, 90 (2),  1351-1366</dc:identifier>
  <dc:language>EN</dc:language>
  <dc:coverage>FIDJI</dc:coverage>
  <dc:coverage>PACIFIQUE</dc:coverage>
</oai_dc:dc>
