Three-component spiro heterocyclization of 1 H -pyrrole-2,3-diones with acetonitriles and 4-hydroxycoumarin. Crystal and molecular structure of ethyl 2-amino-3-cyano-1′-cyclohexyl-2′,5-dioxo-5′-phenyl-1′,2′-dihydro-5 H -spiro-[pyrano[3,2- c ]chromene-4,3′-pyrrole]-4′-carboxylate
Gespeichert in:
Verfasser / Beitragende:
[M. Dmitriev, P. Silaichev, A. Maslivets]
Ort, Verlag, Jahr:
2015
Enthalten in:
Russian Journal of Organic Chemistry, 51/1(2015-01-01), 74-77
Format:
Artikel (online)
Online Zugang:
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| 024 | 7 | 0 | |a 10.1134/S1070428015010121 |2 doi |
| 035 | |a (NATIONALLICENCE)springer-10.1134/S1070428015010121 | ||
| 245 | 0 | 0 | |a Three-component spiro heterocyclization of 1 H -pyrrole-2,3-diones with acetonitriles and 4-hydroxycoumarin. Crystal and molecular structure of ethyl 2-amino-3-cyano-1′-cyclohexyl-2′,5-dioxo-5′-phenyl-1′,2′-dihydro-5 H -spiro-[pyrano[3,2- c ]chromene-4,3′-pyrrole]-4′-carboxylate |h [Elektronische Daten] |c [M. Dmitriev, P. Silaichev, A. Maslivets] |
| 520 | 3 | |a Ethyl 4,5-dioxo-2-phenyl-4,5-dihydro-1H-pyrrole-3-carboxylates reacted with malononitrile (methyl cyanoacetate) and 4-hydroxycoumarin to produce substituted ethyl 2-amino-2′,5-dioxo-5′-phenyl-1′,2′-dihydro-5H-spiro[pyrano[3,2-c]chromene-4,3′-pyrrole]-4′-carboxylates. The crystal and molecular structure of ethyl 2-amino-3-cyano-1′-cyclohexyl-2′,5-dioxo-5′-phenyl-1′,2′-dihydro-5H-spiro[pyrano[3,2-c]chromene-4,3′-pyrrole]-4′-carboxylate was determined by X-ray analysis. | |
| 540 | |a Pleiades Publishing, Ltd., 2015 | ||
| 700 | 1 | |a Dmitriev |D M. |u Perm State National Research University, ul. Bukireva 15, 614990, Perm, Russia |4 aut | |
| 700 | 1 | |a Silaichev |D P. |u Perm State National Research University, ul. Bukireva 15, 614990, Perm, Russia |4 aut | |
| 700 | 1 | |a Maslivets |D A. |u Perm State National Research University, ul. Bukireva 15, 614990, Perm, Russia |4 aut | |
| 773 | 0 | |t Russian Journal of Organic Chemistry |d Pleiades Publishing |g 51/1(2015-01-01), 74-77 |x 1070-4280 |q 51:1<74 |1 2015 |2 51 |o 11178 | |
| 856 | 4 | 0 | |u https://doi.org/10.1134/S1070428015010121 |q text/html |z Onlinezugriff via DOI |
| 898 | |a BK010053 |b XK010053 |c XK010000 | ||
| 900 | 7 | |a Metadata rights reserved |b Springer special CC-BY-NC licence |2 nationallicence | |
| 908 | |D 1 |a research-article |2 jats | ||
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| 950 | |B NATIONALLICENCE |P 856 |E 40 |u https://doi.org/10.1134/S1070428015010121 |q text/html |z Onlinezugriff via DOI | ||
| 950 | |B NATIONALLICENCE |P 700 |E 1- |a Dmitriev |D M. |u Perm State National Research University, ul. Bukireva 15, 614990, Perm, Russia |4 aut | ||
| 950 | |B NATIONALLICENCE |P 700 |E 1- |a Silaichev |D P. |u Perm State National Research University, ul. Bukireva 15, 614990, Perm, Russia |4 aut | ||
| 950 | |B NATIONALLICENCE |P 700 |E 1- |a Maslivets |D A. |u Perm State National Research University, ul. Bukireva 15, 614990, Perm, Russia |4 aut | ||
| 950 | |B NATIONALLICENCE |P 773 |E 0- |t Russian Journal of Organic Chemistry |d Pleiades Publishing |g 51/1(2015-01-01), 74-77 |x 1070-4280 |q 51:1<74 |1 2015 |2 51 |o 11178 | ||