Ontology type: schema:ScholarlyArticle
2010-07
AUTHORSD. M. Musatov, E. V. Starodubtseva, O. V. Turova, D. V. Kurilov, M. G. Vinogradov, A. K. Rakishev, M. I. Struchkova
ABSTRACTDifferent synthetic approaches to functionally substituted benzylamines were examined: reductive amination of alkyl aryl ketones and reduction of aromatic aldehyde oximes. The most efficient procedures were used to prepare a series of previously unknown hydroxy-, alkoxy-, and halogen-substituted benzylamines.
PAGES1021-1028
http://scigraph.springernature.com/pub.10.1134/s1070428010070110
DOIhttp://dx.doi.org/10.1134/s1070428010070110
DIMENSIONShttps://app.dimensions.ai/details/publication/pub.1005896975
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"
},
{
"id": "http://purl.org/au-research/vocabulary/anzsrc-for/2008/0305",
"inDefinedTermSet": "http://purl.org/au-research/vocabulary/anzsrc-for/2008/",
"name": "Organic Chemistry",
"type": "DefinedTerm"
}
],
"author": [
{
"affiliation": {
"alternateName": "Zelinskii Institute of Organic Chemistry, Russian Academy of Sciences, Leninskii pr. 47, 119991, Moscow, Russia",
"id": "http://www.grid.ac/institutes/grid.4886.2",
"name": [
"Zelinskii Institute of Organic Chemistry, Russian Academy of Sciences, Leninskii pr. 47, 119991, Moscow, Russia"
],
"type": "Organization"
},
"familyName": "Musatov",
"givenName": "D. M.",
"id": "sg:person.016040426570.45",
"sameAs": [
"https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.016040426570.45"
],
"type": "Person"
},
{
"affiliation": {
"alternateName": "Zelinskii Institute of Organic Chemistry, Russian Academy of Sciences, Leninskii pr. 47, 119991, Moscow, Russia",
"id": "http://www.grid.ac/institutes/grid.4886.2",
"name": [
"Zelinskii Institute of Organic Chemistry, Russian Academy of Sciences, Leninskii pr. 47, 119991, Moscow, Russia"
],
"type": "Organization"
},
"familyName": "Starodubtseva",
"givenName": "E. V.",
"id": "sg:person.011417521145.28",
"sameAs": [
"https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.011417521145.28"
],
"type": "Person"
},
{
"affiliation": {
"alternateName": "Zelinskii Institute of Organic Chemistry, Russian Academy of Sciences, Leninskii pr. 47, 119991, Moscow, Russia",
"id": "http://www.grid.ac/institutes/grid.4886.2",
"name": [
"Zelinskii Institute of Organic Chemistry, Russian Academy of Sciences, Leninskii pr. 47, 119991, Moscow, Russia"
],
"type": "Organization"
},
"familyName": "Turova",
"givenName": "O. V.",
"id": "sg:person.016555476053.35",
"sameAs": [
"https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.016555476053.35"
],
"type": "Person"
},
{
"affiliation": {
"alternateName": "Zelinskii Institute of Organic Chemistry, Russian Academy of Sciences, Leninskii pr. 47, 119991, Moscow, Russia",
"id": "http://www.grid.ac/institutes/grid.4886.2",
"name": [
"Zelinskii Institute of Organic Chemistry, Russian Academy of Sciences, Leninskii pr. 47, 119991, Moscow, Russia"
],
"type": "Organization"
},
"familyName": "Kurilov",
"givenName": "D. V.",
"id": "sg:person.016245401745.85",
"sameAs": [
"https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.016245401745.85"
],
"type": "Person"
},
{
"affiliation": {
"alternateName": "Zelinskii Institute of Organic Chemistry, Russian Academy of Sciences, Leninskii pr. 47, 119991, Moscow, Russia",
"id": "http://www.grid.ac/institutes/grid.4886.2",
"name": [
"Zelinskii Institute of Organic Chemistry, Russian Academy of Sciences, Leninskii pr. 47, 119991, Moscow, Russia"
],
"type": "Organization"
},
"familyName": "Vinogradov",
"givenName": "M. G.",
"id": "sg:person.0751717767.16",
"sameAs": [
"https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.0751717767.16"
],
"type": "Person"
},
{
"affiliation": {
"alternateName": "Zelinskii Institute of Organic Chemistry, Russian Academy of Sciences, Leninskii pr. 47, 119991, Moscow, Russia",
"id": "http://www.grid.ac/institutes/grid.4886.2",
"name": [
"Zelinskii Institute of Organic Chemistry, Russian Academy of Sciences, Leninskii pr. 47, 119991, Moscow, Russia"
],
"type": "Organization"
},
"familyName": "Rakishev",
"givenName": "A. K.",
"id": "sg:person.012400316113.76",
"sameAs": [
"https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.012400316113.76"
],
"type": "Person"
},
{
"affiliation": {
"alternateName": "Zelinskii Institute of Organic Chemistry, Russian Academy of Sciences, Leninskii pr. 47, 119991, Moscow, Russia",
"id": "http://www.grid.ac/institutes/grid.4886.2",
"name": [
"Zelinskii Institute of Organic Chemistry, Russian Academy of Sciences, Leninskii pr. 47, 119991, Moscow, Russia"
],
"type": "Organization"
},
"familyName": "Struchkova",
"givenName": "M. I.",
"id": "sg:person.01342454222.91",
"sameAs": [
"https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.01342454222.91"
],
"type": "Person"
}
],
"datePublished": "2010-07",
"datePublishedReg": "2010-07-01",
"description": "Different synthetic approaches to functionally substituted benzylamines were examined: reductive amination of alkyl aryl ketones and reduction of aromatic aldehyde oximes. The most efficient procedures were used to prepare a series of previously unknown hydroxy-, alkoxy-, and halogen-substituted benzylamines.",
"genre": "article",
"id": "sg:pub.10.1134/s1070428010070110",
"inLanguage": "en",
"isAccessibleForFree": false,
"isPartOf": [
{
"id": "sg:journal.1136317",
"issn": [
"0514-7492",
"1070-4280"
],
"name": "Russian Journal of Organic Chemistry",
"publisher": "Pleiades Publishing",
"type": "Periodical"
},
{
"issueNumber": "7",
"type": "PublicationIssue"
},
{
"type": "PublicationVolume",
"volumeNumber": "46"
}
],
"keywords": [
"alkyl aryl ketones",
"aryl ketones",
"aromatic aldehydes",
"different synthetic approaches",
"synthetic approach",
"reductive amination",
"benzylamine",
"aldehydes",
"ketones",
"efficient procedure",
"amination",
"alkoxy",
"hydroxy",
"synthesis",
"series",
"reduction",
"procedure",
"system",
"comparison",
"approach"
],
"name": "Comparison of different reducing systems in the synthesis of functionally substituted benzylamines from alkyl aryl ketones and aromatic aldehydes",
"pagination": "1021-1028",
"productId": [
{
"name": "dimensions_id",
"type": "PropertyValue",
"value": [
"pub.1005896975"
]
},
{
"name": "doi",
"type": "PropertyValue",
"value": [
"10.1134/s1070428010070110"
]
}
],
"sameAs": [
"https://doi.org/10.1134/s1070428010070110",
"https://app.dimensions.ai/details/publication/pub.1005896975"
],
"sdDataset": "articles",
"sdDatePublished": "2022-06-01T22:09",
"sdLicense": "https://scigraph.springernature.com/explorer/license/",
"sdPublisher": {
"name": "Springer Nature - SN SciGraph project",
"type": "Organization"
},
"sdSource": "s3://com-springernature-scigraph/baseset/20220601/entities/gbq_results/article/article_521.jsonl",
"type": "ScholarlyArticle",
"url": "https://doi.org/10.1134/s1070428010070110"
}
]
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.10.1134/s1070428010070110'
N-Triples is a line-based linked data format ideal for batch operations.
curl -H 'Accept: application/n-triples' 'https://scigraph.springernature.com/pub.10.1134/s1070428010070110'
Turtle is a human-readable linked data format.
curl -H 'Accept: text/turtle' 'https://scigraph.springernature.com/pub.10.1134/s1070428010070110'
RDF/XML is a standard XML format for linked data.
curl -H 'Accept: application/rdf+xml' 'https://scigraph.springernature.com/pub.10.1134/s1070428010070110'
This table displays all metadata directly associated to this object as RDF triples.
120 TRIPLES
21 PREDICATES
46 URIs
38 LITERALS
6 BLANK NODES