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Reactions of 1-bromo-1-nitro-3,3,3-trichloropropene with O- and N-nucleophiles
Reactions of 1-bromo-1-nitro-3,3,3-trichloropropene with alcohols, benzidine and o -, m -, and p -phenylenediamines was investigated and the reaction conditions were developed. The alkoxylation and amination products and an unusual nitrogen-containing bis-aziridine were obtained; their structures we...
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| Published in: | Russian journal of general chemistry 2010-12, Vol.80 (12), p.2460-2465 |
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| Main Authors: | , , , |
| Format: | Article |
| Language: | English |
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| cited_by | cdi_FETCH-LOGICAL-c288t-6f5b0d9f4fba591636450ab2b85ecac91ffeea08c8d1c56b3f7d71d4c5a59e883 |
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| cites | cdi_FETCH-LOGICAL-c288t-6f5b0d9f4fba591636450ab2b85ecac91ffeea08c8d1c56b3f7d71d4c5a59e883 |
| container_end_page | 2465 |
| container_issue | 12 |
| container_start_page | 2460 |
| container_title | Russian journal of general chemistry |
| container_volume | 80 |
| creator | Stukan’, E. V. Makarenko, S. V. Berkova, G. A. Berestovitskaya, V. M. |
| description | Reactions of 1-bromo-1-nitro-3,3,3-trichloropropene with alcohols, benzidine and
o
-,
m
-, and
p
-phenylenediamines was investigated and the reaction conditions were developed. The alkoxylation and amination products and an unusual nitrogen-containing bis-aziridine were obtained; their structures were characterized by the spectral (IR,
1
H,
13
C NMR, HMQC, and HMBC) methods. |
| doi_str_mv | 10.1134/S1070363210120108 |
| format | article |
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-phenylenediamines was investigated and the reaction conditions were developed. The alkoxylation and amination products and an unusual nitrogen-containing bis-aziridine were obtained; their structures were characterized by the spectral (IR,
1
H,
13
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-phenylenediamines was investigated and the reaction conditions were developed. The alkoxylation and amination products and an unusual nitrogen-containing bis-aziridine were obtained; their structures were characterized by the spectral (IR,
1
H,
13
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o
-,
m
-, and
p
-phenylenediamines was investigated and the reaction conditions were developed. The alkoxylation and amination products and an unusual nitrogen-containing bis-aziridine were obtained; their structures were characterized by the spectral (IR,
1
H,
13
C NMR, HMQC, and HMBC) methods.</abstract><cop>Dordrecht</cop><pub>SP MAIK Nauka/Interperiodica</pub><doi>10.1134/S1070363210120108</doi><tpages>6</tpages></addata></record> |
| fulltext | fulltext |
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| ispartof | Russian journal of general chemistry, 2010-12, Vol.80 (12), p.2460-2465 |
| issn | 1070-3632 1608-3350 |
| language | eng |
| recordid | cdi_crossref_primary_10_1134_S1070363210120108 |
| source | Springer Nature |
| subjects | Chemistry Chemistry and Materials Science Chemistry/Food Science |
| title | Reactions of 1-bromo-1-nitro-3,3,3-trichloropropene with O- and N-nucleophiles |
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