Reaction of 1,2-hydroxylaminooximes with 1,2-diketones. Conversion of 2-acyl-1-hydroxy-3-imidazoline 3-oxides to pyrazine 1,4-dioxides Full article
Journal |
Chemistry of Heterocyclic Compounds
ISSN: 0009-3122 , E-ISSN: 1573-8353 |
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Output data | Year: 1986, Volume: 22, Number: 3, Pages: 268-275 Pages count : 8 DOI: 10.1007/BF00514993 | ||||
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Abstract:
The reaction of acyclic primary and secondary 1,2-hydroxylaminooximes with aliphatic, alkylaromatic, and alkylheteroaromatic 1,2-diketones, depending on the structure of the starting compounds and the reaction conditions, gives derivatives of pyrazine 1,4-dioxide, 2-acyl-1-hydroxy-3-imidazoline 3-oxide, or mixtures thereof. 2-Acyl-1-hydroxy-3-imidazoline 3-oxides have been converted to pyrazine 1,4-dioxides. © 1986 Plenum Publishing Corporation.
Cite:
Grigor'eva L.N.
, Tikhonov A.Y.
, Amitina S.A.
, Volodarskii L.B.
, Korobeinicheva I.K.
Reaction of 1,2-hydroxylaminooximes with 1,2-diketones. Conversion of 2-acyl-1-hydroxy-3-imidazoline 3-oxides to pyrazine 1,4-dioxides
Chemistry of Heterocyclic Compounds. 1986. V.22. N3. P.268-275. DOI: 10.1007/BF00514993 Scopus РИНЦ OpenAlex
Reaction of 1,2-hydroxylaminooximes with 1,2-diketones. Conversion of 2-acyl-1-hydroxy-3-imidazoline 3-oxides to pyrazine 1,4-dioxides
Chemistry of Heterocyclic Compounds. 1986. V.22. N3. P.268-275. DOI: 10.1007/BF00514993 Scopus РИНЦ OpenAlex
Original:
Grigoryeva L.N.
, Tikhonov A.Y.
, Amitina S.A.
, Volodarskii L.B.
, Korobeinicheva I.K.
INTERACTION OF 1,2-HYDROXYLAMINOOXIMES WITH 1,2-DIKETONES - TRANSFORMATION OF 2-ACYL-1-HYDROXY-3-IMIDAZOLINE-3-OXIDES INTO PYRAZINE-1,4-DIOXIDES [in Russian]
Химия гетероциклических соединений/Khimiya Geterotsiklicheskikh Soedinenii. 1986. №3. С.331-338. WOS
INTERACTION OF 1,2-HYDROXYLAMINOOXIMES WITH 1,2-DIKETONES - TRANSFORMATION OF 2-ACYL-1-HYDROXY-3-IMIDAZOLINE-3-OXIDES INTO PYRAZINE-1,4-DIOXIDES [in Russian]
Химия гетероциклических соединений/Khimiya Geterotsiklicheskikh Soedinenii. 1986. №3. С.331-338. WOS
Dates:
Published print: | Mar 1, 1986 |
Identifiers:
Scopus: | 2-s2.0-33750687980 |
Elibrary: | 30831291 |
OpenAlex: | W2094548906 |