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                <identifier>oai:data.mendeley.com/xhg8r4kkyf.1</identifier>
                <datestamp>2019-01-11T18:32:04Z</datestamp>
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            <metadata><oai_dc:dc xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd" 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">
    <dc:creator>Rozo, Gladys</dc:creator>
    <dc:title>H1NMR data of Chemical structure of compounds</dc:title>
    <dc:publisher>Mendeley Data</dc:publisher>
    <dc:description>Both compounds were tested for purity using RP-HPLC with acetonitrile–water (1:5 v/v). Compound 1 showed a signal at a retention time of 15.87 min with some minor signals. Compound 2 showed a signal at a retention time of 21.06 min with some minor signals. 
Compounds were identified by their H1NMR data comparing with those recorded in the literature. The structure corresponding to compound 1 is presented in Figure 5 and agrees with the chemical structure of a catechin. Optical rotation of compound 1 was [α]20 = -53,4; which allows us to conclude that compound 1 is (-)-epicatechin.
The structure corresponding to compound 2, from extract of Hypnea musciformis, is presented in Figure 6 and agrees with the chemical structure of a dihydrochalcone known as phloretin. 
</dc:description>
    <dc:subject>Chemical Compound</dc:subject>
    <dc:contributor>Rozo, Claudia</dc:contributor>
    <dc:contributor>Puyana, Monica</dc:contributor>
    <dc:contributor>Ramos, Freddy A.</dc:contributor>
    <dc:contributor>Almonacid, Carmen</dc:contributor>
    <dc:contributor>Castro, Henry</dc:contributor>
    <dc:type>Dataset</dc:type>
    <dc:identifier>doi:10.17632/xhg8r4kkyf.1</dc:identifier>
    <dc:identifier>oai:data.mendeley.com/xhg8r4kkyf.1</dc:identifier>
    <dc:rights>Creative Commons Attribution 4.0 International</dc:rights>
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    <dc:date>2019-01-11T18:32:04Z</dc:date>
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