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Study of geometric isomerism of ethyl β-aryl(hetaryl)-α-nitroacrylates by 1H NMR spectroscopy method
Features of Z → E isomerization of ethyl α-nitrocinnamates as well as their furyl and thienyl heteroanalogs depending on the nature of the substituent in the β-position of α-nitroacrylates, deuterated solvent and duration of exposure of the sample were studied by means of 1 H NMR spectroscopy.
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| Published in: | Russian journal of general chemistry 2016, Vol.86 (1), p.51-57 |
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| Main Authors: | , , , , |
| Format: | Article |
| Language: | English |
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| cited_by | cdi_FETCH-LOGICAL-c1332-e2ab99129d6571d2932ccfc66b884f3f4732dc9e50349fe2137c52261794bd563 |
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| cites | cdi_FETCH-LOGICAL-c1332-e2ab99129d6571d2932ccfc66b884f3f4732dc9e50349fe2137c52261794bd563 |
| container_end_page | 57 |
| container_issue | 1 |
| container_start_page | 51 |
| container_title | Russian journal of general chemistry |
| container_volume | 86 |
| creator | Baichurin, R. I. Berestovitskaya, D. B. Baichurina, L. V. Aboskalova, N. I. Berestovitskaya, V. M. |
| description | Features of
Z
→
E
isomerization of ethyl α-nitrocinnamates as well as their furyl and thienyl heteroanalogs depending on the nature of the substituent in the β-position of α-nitroacrylates, deuterated solvent and duration of exposure of the sample were studied by means of
1
H NMR spectroscopy. |
| doi_str_mv | 10.1134/S1070363216010102 |
| format | article |
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Z
→
E
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1
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1
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1
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| fulltext | fulltext |
| identifier | ISSN: 1070-3632 |
| ispartof | Russian journal of general chemistry, 2016, Vol.86 (1), p.51-57 |
| issn | 1070-3632 1608-3350 |
| language | eng |
| recordid | cdi_crossref_primary_10_1134_S1070363216010102 |
| source | Springer Nature |
| subjects | Chemistry Chemistry and Materials Science Chemistry/Food Science |
| title | Study of geometric isomerism of ethyl β-aryl(hetaryl)-α-nitroacrylates by 1H NMR spectroscopy method |
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