Form of presentation | Articles in international journals and collections |
Year of publication | 2023 |
Язык | английский |
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Grishaev Denis Yurevich, author
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Andreeva Vera Vladimirovna, author
Ivanova Elizaveta Sergeevna, author
Karpov Sergey Vladimirovich, author
Lodochnikova Olga Aleksandrovna, author
Maryasov Maksim Aleksandrovich, author
Nasakin Oleg Evgenevich, author
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Bibliographic description in the original language |
Nasakin O.E. 3,3,4,4-Tetracyanoalkanones as expedient reagents for utilization of N,N-dimethylhydrazine / O.E. Nasakin, E.S. Ivanova, M. A. Maryasov , V. V. Andreeva , S. V. Karpov, O. A. Lodochnikova, D.Yu. Grishaev // Mendeleev Communications. -2023. - Volume 33 - Issue 6.-Pages 856-857 |
Annotation |
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. |
Keywords |
N,N-dimethylhydrazine, formaldehyde dimethylhydrazone, tetracyanoethylene, 3,3,4,4-tetracyanoalkanones, Thorpe?Ziegler type cyclization, 1,2-dihydro-3H-pyrrole-3,3,4-tricarbonitriles, 4,5-dihydro-1H-pyrrolo[3,4-c]pyridine-3a,7a-dicarbonitriles |
The name of the journal |
MENDELEEV COMMUNICATIONS
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On-line resource for training course |
http://dspace.kpfu.ru/xmlui/bitstream/handle/net/183410/F_1_s2.0_S0959943623003309_mmc1.pdf?sequence=1&isAllowed=y
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URL |
https://www.sciencedirect.com/science/article/pii/S0959943623003309?via%3Dihub |
Please use this ID to quote from or refer to the card |
https://repository.kpfu.ru/eng/?p_id=297784&p_lang=2 |
Resource files | |
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Full metadata record |
Field DC |
Value |
Language |
dc.contributor.author |
Grishaev Denis Yurevich |
ru_RU |
dc.contributor.author |
Andreeva Vera Vladimirovna |
ru_RU |
dc.contributor.author |
Ivanova Elizaveta Sergeevna |
ru_RU |
dc.contributor.author |
Karpov Sergey Vladimirovich |
ru_RU |
dc.contributor.author |
Lodochnikova Olga Aleksandrovna |
ru_RU |
dc.contributor.author |
Maryasov Maksim Aleksandrovich |
ru_RU |
dc.contributor.author |
Nasakin Oleg Evgenevich |
ru_RU |
dc.date.accessioned |
2023-01-01T00:00:00Z |
ru_RU |
dc.date.available |
2023-01-01T00:00:00Z |
ru_RU |
dc.date.issued |
2023 |
ru_RU |
dc.identifier.citation |
Nasakin O.E. 3,3,4,4-Tetracyanoalkanones as expedient reagents for utilization of N,N-dimethylhydrazine / O.E. Nasakin, E.S. Ivanova, M. A. Мaryasov , V. V. Andreeva , S. V. Karpov, O. A. Lodochnikova, D.Yu. Grishaev // Mendeleev Communications. -2023. - Volume 33 - Issue 6.-Pages 856-857 |
ru_RU |
dc.identifier.uri |
https://repository.kpfu.ru/eng/?p_id=297784&p_lang=2 |
ru_RU |
dc.description.abstract |
MENDELEEV COMMUNICATIONS |
ru_RU |
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. |
ru_RU |
dc.language.iso |
ru |
ru_RU |
dc.subject |
N |
ru_RU |
dc.subject |
N-dimethylhydrazine |
ru_RU |
dc.subject |
formaldehyde dimethylhydrazone |
ru_RU |
dc.subject |
tetracyanoethylene |
ru_RU |
dc.subject |
3 |
ru_RU |
dc.subject |
3 |
ru_RU |
dc.subject |
4 |
ru_RU |
dc.subject |
4-tetracyanoalkanones |
ru_RU |
dc.subject |
Thorpe?Ziegler type cyclization |
ru_RU |
dc.subject |
1 |
ru_RU |
dc.subject |
2-dihydro-3H-pyrrole-3 |
ru_RU |
dc.subject |
3 |
ru_RU |
dc.subject |
4-tricarbonitriles |
ru_RU |
dc.subject |
4 |
ru_RU |
dc.subject |
5-dihydro-1H-pyrrolo[3 |
ru_RU |
dc.subject |
4-c]pyridine-3a |
ru_RU |
dc.subject |
7a-dicarbonitriles |
ru_RU |
dc.title |
3,3,4,4-Tetracyanoalkanones as expedient reagents for utilization of N,N-dimethylhydrazine |
ru_RU |
dc.type |
Articles in international journals and collections |
ru_RU |
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