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repchem_organic_name_reactions.ttl
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repchem_organic_name_reactions.ttl
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@prefix : </> .
@prefix dc: <http://purl.org/dc/elements/1.1/> .
@prefix dbr: <http://dbpedia.org/resource/> .
@prefix dct: <http://purl.org/dc/terms/> .
@prefix dul: <http://www.ontologydesignpatterns.org/ont/dul/DUL.owl#> .
@prefix obo: <http://purl.obolibrary.org/obo/> .
@prefix owl: <http://www.w3.org/2002/07/owl#> .
@prefix rdf: <http://www.w3.org/1999/02/22-rdf-syntax-ns#> .
@prefix xml: <http://www.w3.org/XML/1998/namespace> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .
@prefix chem: <http://www.physical-chemistry.com/> .
@prefix foaf: <http://xmlns.com/foaf/0.1/> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix skos: <http://www.w3.org/2004/02/skos/core#> .
@prefix ontology: <http://dbpedia.org/ontology/> .
@prefix property: <http://dbpedia.org/property/> .
@base <http://www.w3.org/2002/07/owl#> .
[ rdf:type owl:Ontology
] .
#################################################################
#
# Classes
#
#################################################################
### http://dbpedia.org/class/yago/NameReactions
<http://dbpedia.org/class/yago/NameReactions> rdf:type owl:Class .
### https://dbpedia.org/resource/Diels–Alder_reaction
<https://dbpedia.org/resource/Diels–Alder_reaction> rdf:type owl:Class ;
rdfs:subClassOf <http://dbpedia.org/class/yago/NameReactions> ;
rdfs:comment "The Diels–Alder reaction is an organic chemical reaction (specifically, a [4+2] cycloaddition) between a conjugated diene and a substituted alkene, commonly termed the dienophile, to form a substituted cyclohexene system. It was first described by Otto Paul Hermann Diels and Kurt Alder in 1928, for which work they were awarded the Nobel Prize in Chemistry in 1950. The Diels–Alder reaction is particularly useful in synthetic organic chemistry as a reliable method for forming 6-membered systems with good control over regio- and stereochemical properties. The underlying concept has also been applied to other π-systems, such as carbonyls and imines, to furnish the corresponding heterocycles, known as the hetero-Diels–Alder reaction. Diels–Alder reactions can be reversible under certain conditions; the reverse reaction is known as the retro-Diels–Alder reaction."@en ;
rdfs:label "Diels-Alder reaction"@en .
### Generated by the OWL API (version 4.2.1.20160306-0033) https://github.com/owlcs/owlapi