Ontology type: schema:ScholarlyArticle
1985-06
AUTHORSG. F. Bannikov, G. A. Nikiforov, V. V. Ershov
ABSTRACTConclusions1-(3,5-Di-tert-butyl-4-hydroxyphenyl)ethylamine and its analogs were prepared in high yield by the Leuckart reaction from the corresponding ketones or aldehyde and ammonium formate or formamide.The reaction of α-methyl-2,6-di-tert-butylmethylquinone with ammonia leads to 1-(3,5-di-tert-butyl-4-hydroxyphenyl)ethylamine.
PAGES1289-1291
http://scigraph.springernature.com/pub.10.1007/bf00956104
DOIhttp://dx.doi.org/10.1007/bf00956104
DIMENSIONShttps://app.dimensions.ai/details/publication/pub.1018202005
JSON-LD is the canonical representation for SciGraph data.
TIP: You can open this SciGraph record using an external JSON-LD service: JSON-LD Playground Google SDTT
[
{
"@context": "https://springernature.github.io/scigraph/jsonld/sgcontext.json",
"about": [
{
"id": "http://purl.org/au-research/vocabulary/anzsrc-for/2008/03",
"inDefinedTermSet": "http://purl.org/au-research/vocabulary/anzsrc-for/2008/",
"name": "Chemical Sciences",
"type": "DefinedTerm"
}
],
"author": [
{
"affiliation": {
"alternateName": "Institute of Chemical Physics, Academy of Sciences of the USSR, Moscow",
"id": "http://www.grid.ac/institutes/grid.424930.8",
"name": [
"Institute of Chemical Physics, Academy of Sciences of the USSR, Moscow"
],
"type": "Organization"
},
"familyName": "Bannikov",
"givenName": "G. F.",
"id": "sg:person.015576457351.97",
"sameAs": [
"https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.015576457351.97"
],
"type": "Person"
},
{
"affiliation": {
"alternateName": "Institute of Chemical Physics, Academy of Sciences of the USSR, Moscow",
"id": "http://www.grid.ac/institutes/grid.424930.8",
"name": [
"Institute of Chemical Physics, Academy of Sciences of the USSR, Moscow"
],
"type": "Organization"
},
"familyName": "Nikiforov",
"givenName": "G. A.",
"id": "sg:person.013720442355.52",
"sameAs": [
"https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.013720442355.52"
],
"type": "Person"
},
{
"affiliation": {
"alternateName": "Institute of Chemical Physics, Academy of Sciences of the USSR, Moscow",
"id": "http://www.grid.ac/institutes/grid.424930.8",
"name": [
"Institute of Chemical Physics, Academy of Sciences of the USSR, Moscow"
],
"type": "Organization"
},
"familyName": "Ershov",
"givenName": "V. V.",
"id": "sg:person.010414742241.10",
"sameAs": [
"https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.010414742241.10"
],
"type": "Person"
}
],
"datePublished": "1985-06",
"datePublishedReg": "1985-06-01",
"description": "Conclusions1-(3,5-Di-tert-butyl-4-hydroxyphenyl)ethylamine and its analogs were prepared in high yield by the Leuckart reaction from the corresponding ketones or aldehyde and ammonium formate or formamide.The reaction of \u03b1-methyl-2,6-di-tert-butylmethylquinone with ammonia leads to 1-(3,5-di-tert-butyl-4-hydroxyphenyl)ethylamine.",
"genre": "article",
"id": "sg:pub.10.1007/bf00956104",
"inLanguage": "en",
"isAccessibleForFree": false,
"isPartOf": [
{
"id": "sg:journal.1022309",
"issn": [
"1026-3500",
"1066-5285"
],
"name": "Russian Chemical Bulletin",
"publisher": "Springer Nature",
"type": "Periodical"
},
{
"issueNumber": "6",
"type": "PublicationIssue"
},
{
"type": "PublicationVolume",
"volumeNumber": "34"
}
],
"keywords": [
"Leuckart reaction",
"ammonium formate",
"carbonyl derivatives",
"Conclusions1",
"di",
"analogues",
"high yield",
"yield",
"reaction",
"ketones",
"aldehydes",
"formate",
"formamide",
"methyl",
"ammonia",
"butyl-4",
"derivatives",
"butylphenol"
],
"name": "Leuckart reaction of carbonyl derivatives of 2,6-di-tert-butylphenol",
"pagination": "1289-1291",
"productId": [
{
"name": "dimensions_id",
"type": "PropertyValue",
"value": [
"pub.1018202005"
]
},
{
"name": "doi",
"type": "PropertyValue",
"value": [
"10.1007/bf00956104"
]
}
],
"sameAs": [
"https://doi.org/10.1007/bf00956104",
"https://app.dimensions.ai/details/publication/pub.1018202005"
],
"sdDataset": "articles",
"sdDatePublished": "2022-05-10T09:43",
"sdLicense": "https://scigraph.springernature.com/explorer/license/",
"sdPublisher": {
"name": "Springer Nature - SN SciGraph project",
"type": "Organization"
},
"sdSource": "s3://com-springernature-scigraph/baseset/20220509/entities/gbq_results/article/article_187.jsonl",
"type": "ScholarlyArticle",
"url": "https://doi.org/10.1007/bf00956104"
}
]
Download the RDF metadata as: json-ld nt turtle xml License info
JSON-LD is a popular format for linked data which is fully compatible with JSON.
curl -H 'Accept: application/ld+json' 'https://scigraph.springernature.com/pub.10.1007/bf00956104'
N-Triples is a line-based linked data format ideal for batch operations.
curl -H 'Accept: application/n-triples' 'https://scigraph.springernature.com/pub.10.1007/bf00956104'
Turtle is a human-readable linked data format.
curl -H 'Accept: text/turtle' 'https://scigraph.springernature.com/pub.10.1007/bf00956104'
RDF/XML is a standard XML format for linked data.
curl -H 'Accept: application/rdf+xml' 'https://scigraph.springernature.com/pub.10.1007/bf00956104'
This table displays all metadata directly associated to this object as RDF triples.
86 TRIPLES
21 PREDICATES
43 URIs
36 LITERALS
6 BLANK NODES