Multi-channel annulation of acetylene with 3-methyl-7,8-dihydro-cinnolin-5(6H)-one oxime in the KOH/DMSO superbasic system Full article
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Mendeleev Communications
ISSN: 0959-9436 |
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Output data | Year: 2017, Volume: 27, Number: 4, Pages: 344-345 Pages count : 2 DOI: 10.1016/j.mencom.2017.07.007 | ||||
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Abstract:
Acetylene in the KOH/DMSO system (1 bar, 140 degrees C, 12 h) is annulated with 3-methyl-7,8-dihydrocinnolin-5(6H)-one oxime in several directions: along with the building up of pyrrole fragment over cyclohexane ring, transformation of the oxime function to the amino one occurs. This amine undergoes other annulations to form tricyclic compounds with pyridine moieties.
Cite:
Petrova O.V.
, Sobenina L.N.
, Ushakov I.A.
, Budaev A.B.
, Ivanov A.V.
, Samsonov V.A.
, Tikhonov A.Y.
, Trofimov B.A.
Multi-channel annulation of acetylene with 3-methyl-7,8-dihydro-cinnolin-5(6H)-one oxime in the KOH/DMSO superbasic system
Mendeleev Communications. 2017. V.27. N4. P.344-345. DOI: 10.1016/j.mencom.2017.07.007 WOS Scopus РИНЦ
Multi-channel annulation of acetylene with 3-methyl-7,8-dihydro-cinnolin-5(6H)-one oxime in the KOH/DMSO superbasic system
Mendeleev Communications. 2017. V.27. N4. P.344-345. DOI: 10.1016/j.mencom.2017.07.007 WOS Scopus РИНЦ
Dates:
Published print: | Jul 1, 2017 |
Identifiers:
Web of science | WOS:000408783800006 |
Scopus | 2-s2.0-85026405006 |
Elibrary | 31062221 |
OpenAlex | W2742042942 |