Vladimir V Ershov

Ontology type: schema:Person     

Person Info


Vladimir V



Publications in SciGraph latest 50 shown

  • 2002-10 Isotopic Study of the Formation of Phenoxazine Derivatives in the Transformations of 3,5-Di-tert-Butylcatechol Adsorbed in Thin SiO2-nTiO2 Layers in the Air in CHEMISTRY OF HETEROCYCLIC COMPOUNDS
  • 2000-08 Synthesis of heterocyclic derivatives of 3,6-di-tert-butyl-o-benzoquinone by catalytic dehydrocondensation with ethylene glycol, glycerol, and diethanolamine in CHEMISTRY OF HETEROCYCLIC COMPOUNDS
  • 2000-06 Solid-phase oxidation of 2,4-Di-tert-butylphenol and 3,6-Di-tert-butylpyrocatechol in the presence of alkali and alkaline earth metal halides under elastic deformation in RUSSIAN JOURNAL OF ELECTROCHEMISTRY
  • 1998-10 Hydroxylation of substituted diatomic phenols and their derivatives in RUSSIAN CHEMICAL BULLETIN
  • 1998-10 ESR study of products of transformation of 3,6-tert-butylpyrocatechol on alumina, zinca, silica, and titania in RUSSIAN CHEMICAL BULLETIN
  • 1997-07 Oxidation of 2-dialkylaminomethyl-4,6-di-tert-butylphenols in RUSSIAN CHEMICAL BULLETIN
  • 1997-02 The formation of nitrogen-containing organic compounds in the transformations of 3,5-di-tert-butylpyrocatechol adsorbed on thin layers of SiO2 in air in RUSSIAN CHEMICAL BULLETIN
  • 1996-08 Rearrangement fragmentation of aldoxime to isocyanide in RUSSIAN CHEMICAL BULLETIN
  • 1996-06 Reactivity in solid phase. Transformations of 2,4-di-tert-butylphenol and its derivatives under elastic deformation conditions in RUSSIAN CHEMICAL BULLETIN
  • 1996-05 Solid-phase bromination of hindered phenols in RUSSIAN CHEMICAL BULLETIN
  • 1996-04-01 The solid-phase anhydroheterocyclization of 2,2′-dihydroxy-3,3′,5,5′-tetra-tert-butylbiphenyl under the action of dioxane dibromide in RUSSIAN CHEMICAL BULLETIN
  • 1996-02 Some heterocyclic derivatives of sterically hindered phenols in RUSSIAN CHEMICAL BULLETIN
  • 1995-09 Reactions of isomeric 3,6- and 3,5-di-tert-butyl-ortho-benzoquinones with NH3 in RUSSIAN CHEMICAL BULLETIN
  • 1995-08 Synthesis and structure of anhydrodimers of salicylaldehydes in RUSSIAN CHEMICAL BULLETIN
  • 1994-10 The solid-phase catalytic oxydation of 2-hydroxy-3,5-di-tert-butylbenzyl alcohol in RUSSIAN CHEMICAL BULLETIN
  • 1994-01 Acetyl chloride-3,5-di(tert-butyl)-4-hydroxy-N,N-dimethylbenzylamme salt in the benzylation of organic and inorganic sulfur-containing compounds in RUSSIAN CHEMICAL BULLETIN
  • 1993-03 Salts of acyl halides and 3, 5-di-tert-butyl-4-hydroxy-N, N-dimethylbenzylamine in benzylation reactions in RUSSIAN CHEMICAL BULLETIN
  • 1992-10 Semi-hindered phenols. 1. Synthesis of 3,5-di-tert-butylsalicylic aldehyde in RUSSIAN CHEMICAL BULLETIN
  • 1991-10 Regiocontrolled nitration of di(tert-butyl)phenols in RUSSIAN CHEMICAL BULLETIN
  • 1990-09 Hydroxymethylation of 2,4-di-tert-butylphenol in RUSSIAN CHEMICAL BULLETIN
  • 1990-09 Adsorption of hydrogen on zeolite NaA at low temperatures in RUSSIAN CHEMICAL BULLETIN
  • 1990-08 Sodium persulfate in solid phase organic synthesis in RUSSIAN CHEMICAL BULLETIN
  • 1990-05 Redox reactions of 3,6-di-tert-butyl-ortho-benzoquinone, catalyzed by tetrafluorosilane in RUSSIAN CHEMICAL BULLETIN
  • 1989-12 Substituted dialkylaminomethylphenols in an exchange reaction with carboxylic acid anhydrides in RUSSIAN CHEMICAL BULLETIN
  • 1989-05 Formation of 3,6-di-tert-butyl-2-hydroxyphenoxyl radicals upon the inhibition of polymerization of methyl methacrylate by the system containing 3,6-di-tert-butylpryocatechol and 3,6-di-tert-butyl-1,2-benzoquinone in RUSSIAN CHEMICAL BULLETIN
  • 1989-01 Explosive chemical transformations of 4-bromo-2,4,6-tri-tert-butylcyclohexa-2,5-diene-1-one in strong uniaxial compression in RUSSIAN CHEMICAL BULLETIN
  • 1988-09 Anomalous Duff reaction with 2,4-di-tert-butylphenol in RUSSIAN CHEMICAL BULLETIN
  • 1988-05 Radical-cations of 3,6-di-tert-butylpyrocatechol esters in RUSSIAN CHEMICAL BULLETIN
  • 1987-10 Isomeric di-tert-butylorthophenylenequinols in redox reactions in RUSSIAN CHEMICAL BULLETIN
  • 1986-12 Reaction of 3,6-di-tert-butyl-ortho-benzoquinone with zinc and aluminum under high pressure and shear deformation conditions in RUSSIAN CHEMICAL BULLETIN
  • 1986-09 Stimulation of an intermolecular redox reaction by the combined action of high pressure and shear deformation in RUSSIAN CHEMICAL BULLETIN
  • 1986-03 Reaction of 2,4,6-tri-tert-butylphenoxyl with oxygen in the presence of metal compounds in RUSSIAN CHEMICAL BULLETIN
  • 1986-03 Oxidative heterocyclization of 6-bromo-2,4-di-tert-butylphenol in RUSSIAN CHEMICAL BULLETIN
  • 1986-01 Oxidation and alkoxylation of 3,6-di-tert-butyl-pyrocatechol catalyzed by manganese diacetate in RUSSIAN CHEMICAL BULLETIN
  • 1985-06 Leuckart reaction of carbonyl derivatives of 2,6-di-tert-butylphenol in RUSSIAN CHEMICAL BULLETIN
  • 1985-06 2-alkoxy-3,6-di-tert-butylphenoxyls in RUSSIAN CHEMICAL BULLETIN
  • 1985-05 Reaction of 6,8-di-tert-butyl-1-oxaspiro[4.5]deca-5,8-diene-2,7-dione with amines in RUSSIAN CHEMICAL BULLETIN
  • 1984-10 Oxidation of sterically hindered phenols by manganese triacetate and potassium bichromate in neutral and acidic media in RUSSIAN CHEMICAL BULLETIN
  • 1984-07 Ortho-esters based on 3, 6-di-tertbutylpyrocatechol in RUSSIAN CHEMICAL BULLETIN
  • 1984-07 Reaction of 3,6-di-tert-butylpyrocatechol with thionyl chloride in the presence of dimethylformamide in RUSSIAN CHEMICAL BULLETIN
  • 1984-06 Direct synthesis of tris(3,6-di-tert-butylorthobenzoquinono)chromium under high pressure and shearing strain conditions in RUSSIAN CHEMICAL BULLETIN
  • 1984-02 Conversion of 3,6-di-tert-butylorthobenzoquinone in bridgman presses in RUSSIAN CHEMICAL BULLETIN
  • 1983-06 Halogenation of 3,6-di-tert-butylpyrocatechol with retention of the alkyl substituents in RUSSIAN CHEMICAL BULLETIN
  • 1983-03 Dienone-phenol conversions of 4-x-substituted 4-hydroxy-2,6-di-tert-butylcyclohexa-2,5-dienones in acid media in RUSSIAN CHEMICAL BULLETIN
  • 1983-02 Reaction of o-benzoquinones with benzylidenetriphenylphosphorane under the conditions of the common effect of high pressure and shear deformation in RUSSIAN CHEMICAL BULLETIN
  • 1983-02 Migration of alkyl groups of o-tert-butyl-substituted hydroxyaromatic compounds under high pressure in combination with shearing stress in RUSSIAN CHEMICAL BULLETIN
  • 1983-01 Kinetics and mechanism of alkylation of sterically hindered phenol salts by functionally substituted olefins in RUSSIAN CHEMICAL BULLETIN
  • 1982-07 Oxidation of 4-substituted 2,6-di-tert-butylphenols by oxygen in alkaline medium in RUSSIAN CHEMICAL BULLETIN
  • 1982-07 Reaction of 6, 8-di-tert-butylspiro[4,5]deca-1-oxa-5,8-diene-2,7-dione with acid agents in RUSSIAN CHEMICAL BULLETIN
  • 1982-03 Atypical case of dienone-phenol isomerization in RUSSIAN CHEMICAL BULLETIN
  • 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", 
        "affiliation": [
            "affiliation": {
              "id": "http://www.grid.ac/institutes/grid.4886.2", 
              "type": "Organization"
            "isCurrent": true, 
            "type": "OrganizationRole"
            "id": "http://www.grid.ac/institutes/grid.70465.30", 
            "type": "Organization"
            "id": "http://www.grid.ac/institutes/grid.6988.f", 
            "type": "Organization"
            "id": "http://www.grid.ac/institutes/grid.418751.e", 
            "type": "Organization"
            "id": "http://www.grid.ac/institutes/grid.418949.9", 
            "type": "Organization"
            "id": "http://www.grid.ac/institutes/grid.482651.c", 
            "type": "Organization"
            "id": "http://www.grid.ac/institutes/grid.466123.4", 
            "type": "Organization"
            "id": "http://www.grid.ac/institutes/grid.465443.4", 
            "type": "Organization"
            "id": "http://www.grid.ac/institutes/grid.424930.8", 
            "type": "Organization"
            "id": "http://www.grid.ac/institutes/grid.439283.7", 
            "type": "Organization"
        "familyName": "Ershov", 
        "givenName": "Vladimir V", 
        "id": "sg:person.010414742241.10", 
        "sameAs": [
        "sdDataset": "persons", 
        "sdDatePublished": "2022-01-01T19:58", 
        "sdLicense": "https://scigraph.springernature.com/explorer/license/", 
        "sdPublisher": {
          "name": "Springer Nature - SN SciGraph project", 
          "type": "Organization"
        "sdSource": "s3://com-springernature-scigraph/baseset/20220101/entities/gbq_results/person/person_910.jsonl", 
        "type": "Person"

    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/person.010414742241.10'

    N-Triples is a line-based linked data format ideal for batch operations.

    curl -H 'Accept: application/n-triples' 'https://scigraph.springernature.com/person.010414742241.10'

    Turtle is a human-readable linked data format.

    curl -H 'Accept: text/turtle' 'https://scigraph.springernature.com/person.010414742241.10'

    RDF/XML is a standard XML format for linked data.

    curl -H 'Accept: application/rdf+xml' 'https://scigraph.springernature.com/person.010414742241.10'


    This table displays all metadata directly associated to this object as RDF triples.

    34 TRIPLES      10 PREDICATES      20 URIs      7 LITERALS      2 BLANK NODES

    Subject Predicate Object
    1 sg:person.010414742241.10 schema:affiliation N9956f4ae1c5f46b3b7fcd40e1ae10772
    2 grid-institutes:grid.418751.e
    3 grid-institutes:grid.418949.9
    4 grid-institutes:grid.424930.8
    5 grid-institutes:grid.439283.7
    6 grid-institutes:grid.465443.4
    7 grid-institutes:grid.466123.4
    8 grid-institutes:grid.482651.c
    9 grid-institutes:grid.6988.f
    10 grid-institutes:grid.70465.30
    11 schema:familyName Ershov
    12 schema:givenName Vladimir V
    13 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.010414742241.10
    14 schema:sdDatePublished 2022-01-01T19:58
    15 schema:sdLicense https://scigraph.springernature.com/explorer/license/
    16 schema:sdPublisher N86183954a06042aeaa7ce9b09e1c66ee
    17 sgo:license sg:explorer/license/
    18 sgo:sdDataset persons
    19 rdf:type schema:Person
    20 N86183954a06042aeaa7ce9b09e1c66ee schema:name Springer Nature - SN SciGraph project
    21 rdf:type schema:Organization
    22 N9956f4ae1c5f46b3b7fcd40e1ae10772 schema:affiliation grid-institutes:grid.4886.2
    23 sgo:isCurrent true
    24 rdf:type schema:OrganizationRole
    25 grid-institutes:grid.418751.e schema:Organization
    26 grid-institutes:grid.418949.9 schema:Organization
    27 grid-institutes:grid.424930.8 schema:Organization
    28 grid-institutes:grid.439283.7 schema:Organization
    29 grid-institutes:grid.465443.4 schema:Organization
    30 grid-institutes:grid.466123.4 schema:Organization
    31 grid-institutes:grid.482651.c schema:Organization
    32 grid-institutes:grid.4886.2 schema:Organization
    33 grid-institutes:grid.6988.f schema:Organization
    34 grid-institutes:grid.70465.30 schema:Organization

    Preview window. Press ESC to close (or click here)