{"?xml":{"@version":"1.0"},"edm:RDF":{"@xmlns:dc":"http://purl.org/dc/elements/1.1/","@xmlns:edm":"http://www.europeana.eu/schemas/edm/","@xmlns:wgs84_pos":"http://www.w3.org/2003/01/geo/wgs84_pos","@xmlns:foaf":"http://xmlns.com/foaf/0.1/","@xmlns:rdaGr2":"http://rdvocab.info/ElementsGr2","@xmlns:oai":"http://www.openarchives.org/OAI/2.0/","@xmlns:owl":"http://www.w3.org/2002/07/owl#","@xmlns:rdf":"http://www.w3.org/1999/02/22-rdf-syntax-ns#","@xmlns:ore":"http://www.openarchives.org/ore/terms/","@xmlns:skos":"http://www.w3.org/2004/02/skos/core#","@xmlns:dcterms":"http://purl.org/dc/terms/","edm:WebResource":[{"@rdf:about":"http://www.dlib.si/stream/URN:NBN:SI:doc-APL1CVJU/ac6dc3df-b2b3-42e2-a333-28d080f46d6e/HTML","dcterms:extent":"16 KB"},{"@rdf:about":"http://www.dlib.si/stream/URN:NBN:SI:doc-APL1CVJU/67be5457-fdba-4ba3-9d55-a866ff145502/PDF","dcterms:extent":"164 KB"},{"@rdf:about":"http://www.dlib.si/stream/URN:NBN:SI:doc-APL1CVJU/3277a445-995c-4f17-a889-fa2422ed8193/TEXT","dcterms:extent":"13 KB"}],"edm:TimeSpan":{"@rdf:about":"1998-2025","edm:begin":{"@xml:lang":"en","#text":"1998"},"edm:end":{"@xml:lang":"en","#text":"2025"}},"edm:ProvidedCHO":{"@rdf:about":"URN:NBN:SI:doc-APL1CVJU","dcterms:isPartOf":[{"@rdf:resource":"https://www.dlib.si/details/URN:NBN:SI:spr-KC6O72BG"},{"@xml:lang":"sl","#text":"Acta chimica slovenica"}],"dcterms:issued":"2002","dc:creator":["Obreza, Aleš","Urleb, Uroš"],"dc:format":[{"@xml:lang":"sl","#text":"številka:3"},{"@xml:lang":"sl","#text":"letnik:49"},{"@xml:lang":"sl","#text":"7 strani"},{"@xml:lang":"sl","#text":"str. 605-611"}],"dc:identifier":["COBISSID:1172593","ISSN:1318-0207","URN:URN:NBN:SI:doc-APL1CVJU"],"dc:language":"en","dc:publisher":{"@xml:lang":"sl","#text":"Slovensko kemijsko društvo"},"dc:subject":[{"@xml:lang":"sl","#text":"analiza"},{"@xml:lang":"sl","#text":"hidrazinkarboskilati"},{"@xml:lang":"sl","#text":"hidrazoni"},{"@xml:lang":"sl","#text":"sinteza"}],"dcterms:temporal":{"@rdf:resource":"1998-2025"},"dc:title":{"@xml:lang":"sl","#text":"A new synthesis of substituted benzaldehyde N-(E)-phenylmethylidenehydrazones| Nova sinteza substituiranih benzaldehid N-(E)-fenilmetiliden-hidrazonov|"},"dc:description":[{"@xml:lang":"sl","#text":"Reaction of substituted tert-butyl 2-(phenylmethylidene)-1-hydrazinecarboxylates with gaseous HCl in various anhydrous solvents affords benzaldehyde N-(phenylmethylidene)-hydrazones in very good yields. A series of substituted benzaldehydes was used for the preparation of this type of compounds. The structure of the resulting compounds was investigated by 1H-NMR, IR and MS spectra"},{"@xml:lang":"sl","#text":"Pri reakciji substituiranih terc-butil 2-(fenilmetiliden)-1-hidrazinkarboksilatov s plinastim HCI v različnih brezvodnih topilih dobimo benzalehid N-(fenilmetiliden)hidrazone z zelo visokimi izkoristki. Za sintezo spojin tega tipa smo uporabili rsto različnih subsituiranih benzaldehidov. Strukturo nastalih produktov smo dokazali z uporabo H-NMR in IR spektroskopije ter masne spektrometrije"}],"edm:type":"TEXT","dc:type":[{"@xml:lang":"sl","#text":"znanstveno časopisje"},{"@xml:lang":"en","#text":"journals"},{"@rdf:resource":"http://www.wikidata.org/entity/Q361785"}]},"ore:Aggregation":{"@rdf:about":"http://www.dlib.si/?URN=URN:NBN:SI:doc-APL1CVJU","edm:aggregatedCHO":{"@rdf:resource":"URN:NBN:SI:doc-APL1CVJU"},"edm:isShownBy":{"@rdf:resource":"http://www.dlib.si/stream/URN:NBN:SI:doc-APL1CVJU/67be5457-fdba-4ba3-9d55-a866ff145502/PDF"},"edm:rights":{"@rdf:resource":"http://creativecommons.org/licenses/by/4.0/"},"edm:provider":"Slovenian National E-content Aggregator","edm:intermediateProvider":{"@xml:lang":"en","#text":"National and University Library of Slovenia"},"edm:dataProvider":{"@xml:lang":"sl","#text":"Slovensko kemijsko društvo"},"edm:object":{"@rdf:resource":"http://www.dlib.si/streamdb/URN:NBN:SI:doc-APL1CVJU/maxi/edm"},"edm:isShownAt":{"@rdf:resource":"http://www.dlib.si/details/URN:NBN:SI:doc-APL1CVJU"}}}}