2-(4-nitrophenyl)oxirane amino derivatives in heterocyclization reactions
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| 024 | 7 | 0 | |a 10.1134/S1070428015080096 |2 doi |
| 035 | |a (NATIONALLICENCE)springer-10.1134/S1070428015080096 | ||
| 100 | 1 | |a Pal'chikov |D V. |u Oles' Honchar Dnepropetrovsk National University, pr. Gagarina 72, 49010, Dnepropetrovsk, Ukraine |4 aut | |
| 245 | 1 | 0 | |a 2-(4-nitrophenyl)oxirane amino derivatives in heterocyclization reactions |h [Elektronische Daten] |c [V. Pal'chikov] |
| 520 | 3 | |a Reactions of 2-amino-1-(4-nitrophenyl)ethanol with various electrophilic reagents led to the formation of oxazaheterocycles (1,3-oxazolidin-2-one, 1,3-oxazolidine, morpholin-2-, -3-one, and -2,3-dione). In reactions of 2-{(bicyclo[2.2.1]hept-5-en-2-ylmethyl)amino}-1-(4-nitrophenyl)ethan-1-ol with carbonyldiimidazole, oxalyl chloride, benzaldehyde, and formaldehyde the corresponding derivatives of 1,3-oxazolidin-2- one, morpholin-2,3-dione, and 1,3-oxazolidine were obtained. | |
| 540 | |a Pleiades Publishing, Ltd., 2015 | ||
| 773 | 0 | |t Russian Journal of Organic Chemistry |d Pleiades Publishing |g 51/8(2015-08-01), 1114-1118 |x 1070-4280 |q 51:8<1114 |1 2015 |2 51 |o 11178 | |
| 856 | 4 | 0 | |u https://doi.org/10.1134/S1070428015080096 |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 | ||
| 949 | |B NATIONALLICENCE |F NATIONALLICENCE |b NL-springer | ||
| 950 | |B NATIONALLICENCE |P 856 |E 40 |u https://doi.org/10.1134/S1070428015080096 |q text/html |z Onlinezugriff via DOI | ||
| 950 | |B NATIONALLICENCE |P 100 |E 1- |a Pal'chikov |D V. |u Oles' Honchar Dnepropetrovsk National University, pr. Gagarina 72, 49010, Dnepropetrovsk, Ukraine |4 aut | ||
| 950 | |B NATIONALLICENCE |P 773 |E 0- |t Russian Journal of Organic Chemistry |d Pleiades Publishing |g 51/8(2015-08-01), 1114-1118 |x 1070-4280 |q 51:8<1114 |1 2015 |2 51 |o 11178 | ||