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3,3,4,4-Tetracyanoalkanones as expedient reagents for utilization of N,N-dimethylhydrazine

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dc.contributor Казанский федеральный университет
dc.contributor.author Nasakin Oleg Evgenevich
dc.contributor.author Ivanova Elizaveta Sergeevna
dc.contributor.author Maryasov Maksim Aleksandrovich
dc.contributor.author Andreeva Vera Vladimirovna
dc.contributor.author Karpov Sergey Vladimirovich
dc.contributor.author Lodochnikova Olga Aleksandrovna
dc.contributor.author Grishaev Denis Yurievich
dc.date.accessioned 2024-04-05T10:04:08Z
dc.date.available 2024-04-05T10:04:08Z
dc.date.issued 2023
dc.identifier.citation 3,3,4,4-Tetracyanoalkanones as expedient reagents for utilization of N,N-dimethylhydrazine / O.E. Nasakin, [et al.] // Mendeleev Communications. - 2023. - Vol. 33, Is. 6.- PP. 856-857.
dc.identifier.uri https://dspace.kpfu.ru/xmlui/handle/net/183410
dc.description.abstract To utilize N,N-dimethylhydrazine, the corresponding +formaldehyde hydrazone was reacted with 1,1,2,2-tetra-cyanoethane or 3,3,4,4-tetracyanoalkanones. The first process yielded 5-amino-1-dimethylamino-1,2-dihydro-3H-pyrrole-3,3,4-tricarbonitrile while the second afforded pyrrolo[3,4-c]quinolone multifunctional derivatives. These resultant products hold promise in molecular design and pharmaceutical chemistry.
dc.language.iso en
dc.relation.ispartofseries MENDELEEV COMMUNICATIONS
dc.rights открытый доступ
dc.subject N
dc.subject N-dimethylhydrazine
dc.subject formaldehyde dimethylhydrazone
dc.subject tetracyanoethylene
dc.subject 3
dc.subject 3
dc.subject 4
dc.subject 4-tetracyanoalkanones
dc.subject Thorpe?Ziegler type cyclization
dc.subject 1
dc.subject 2-dihydro-3H-pyrrole-3
dc.subject 3
dc.subject 4-tricarbonitriles
dc.subject 4
dc.subject 5-dihydro-1H-pyrrolo[3
dc.subject 4-c]pyridine-3a
dc.subject 7a-dicarbonitriles
dc.subject.other Химия
dc.title 3,3,4,4-Tetracyanoalkanones as expedient reagents for utilization of N,N-dimethylhydrazine
dc.type Article
dc.contributor.org НОЦ фармацевтики
dc.description.pages 856-857
dc.relation.ispartofseries-issue 6
dc.relation.ispartofseries-volume 33
dc.pub-id 297784
dc.identifier.doi 10.1016/j.mencom.2023.10.039


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