<?xml version="1.0"?>
<?xml-stylesheet type="text/xsl" href="https://ontobee.org/ontology/view/RXNO?iri=http://purl.obolibrary.org/obo/RXNO_0000668"?>
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    <AnnotationProperty rdf:about="http://purl.obolibrary.org/obo/IAO_0000115"/>
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    <!-- http://purl.obolibrary.org/obo/RXNO_0000423 -->

    <ObjectProperty rdf:about="http://purl.obolibrary.org/obo/RXNO_0000423">
        <rdfs:label rdf:datatype="http://www.w3.org/2001/XMLSchema#string">has specified product</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/RXNO_0000424 -->

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        <rdfs:label rdf:datatype="http://www.w3.org/2001/XMLSchema#string">has specified reactant</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/CHEBI_15734 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/CHEBI_15734">
        <rdfs:label rdf:datatype="http://www.w3.org/2001/XMLSchema#string">primary alcohol</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/CHEBI_17087 -->

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    <!-- http://purl.obolibrary.org/obo/CHEBI_17478 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/CHEBI_17478">
        <rdfs:label rdf:datatype="http://www.w3.org/2001/XMLSchema#string">aldehyde</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/CHEBI_35681 -->

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        <rdfs:label rdf:datatype="http://www.w3.org/2001/XMLSchema#string">secondary alcohol</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/RXNO_0000012 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/RXNO_0000012">
        <rdfs:label rdf:datatype="http://www.w3.org/2001/XMLSchema#string">functional group oxidation</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/RXNO_0000668 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/RXNO_0000668">
        <rdfs:label xml:lang="en">Albright-Goldman oxidation</rdfs:label>
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        <dc:date rdf:datatype="http://www.w3.org/2001/XMLSchema#dateTime">2021-11-15T09:30:47Z</dc:date>
        <ns4:IAO_0000115 rdf:datatype="http://www.w3.org/2001/XMLSchema#string">A particularly mild oxidation method in which, for example, dimethyl sulfoxide and acetic anhydride can be used as oxidizing agents to selectively produce aldehydes from primary alcohols without further oxidation to carboxylic acids. Analogously, secondary alcohols can be oxidized to form ketones.</ns4:IAO_0000115>
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<!-- Generated by the OWL API (version 3.2.4.1806) http://owlapi.sourceforge.net -->



