The preparation of 1-(β-naphthyl)-3-ferrocenylpyrazole-4-carbaldehyde and syntheses on the base of it
Synthesis of 1-(β-naphthyl)-3-ferrocenyl pyrazole-4-carbaldehyde was carried out from acetylferrocene and naphthalen-2-ylhydrazine followed by intramolecular cyclization under Vilsmeier-Haack conditions. The reaction of reductive amination of aldehydes obtained with primary and secondary amines incl...
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| Format: | Article |
| Language: | Russian |
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MIREA - Russian Technological University
2009-04-01
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| Series: | Тонкие химические технологии |
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| Online Access: | https://www.finechem-mirea.ru/jour/article/view/1113 |
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| author | E. Yu. Osipova A. A. Simenel A. N. Rodionov V. V. Kachala K. Ya. Zherebker |
| author_facet | E. Yu. Osipova A. A. Simenel A. N. Rodionov V. V. Kachala K. Ya. Zherebker |
| author_sort | E. Yu. Osipova |
| collection | DOAJ |
| description | Synthesis of 1-(β-naphthyl)-3-ferrocenyl pyrazole-4-carbaldehyde was carried out from acetylferrocene and naphthalen-2-ylhydrazine followed by intramolecular cyclization under Vilsmeier-Haack conditions. The reaction of reductive amination of aldehydes obtained with primary and secondary amines including methyl esters of amino acids was studied. |
| format | Article |
| id | doaj-art-059db467a33d4b659efde0cea9c8df24 |
| institution | Matheson Library |
| issn | 2410-6593 2686-7575 |
| language | Russian |
| publishDate | 2009-04-01 |
| publisher | MIREA - Russian Technological University |
| record_format | Article |
| series | Тонкие химические технологии |
| spelling | doaj-art-059db467a33d4b659efde0cea9c8df242025-08-04T10:19:32ZrusMIREA - Russian Technological UniversityТонкие химические технологии2410-65932686-75752009-04-01421001051107The preparation of 1-(β-naphthyl)-3-ferrocenylpyrazole-4-carbaldehyde and syntheses on the base of itE. Yu. Osipova0A. A. Simenel1A. N. Rodionov2V. V. Kachala3K. Ya. Zherebker4МИТХТ им. М.В. Ломоносова, 119571, Москва, пр-т Вернадского, д. 86Институт элементоорганических соединений им. А.Н. Несмеянова РАНИнститут элементоорганических соединений им. А.Н. Несмеянова РАНИнститут органической химии им. Н.Д. Зелинского РАНМИТХТ им. М.В. Ломоносова, 119571, Москва, пр-т Вернадского, д. 86Synthesis of 1-(β-naphthyl)-3-ferrocenyl pyrazole-4-carbaldehyde was carried out from acetylferrocene and naphthalen-2-ylhydrazine followed by intramolecular cyclization under Vilsmeier-Haack conditions. The reaction of reductive amination of aldehydes obtained with primary and secondary amines including methyl esters of amino acids was studied.https://www.finechem-mirea.ru/jour/article/view/1113acetylferrocenevilsmeier-haack reagentpyrazolesreductive aminationtriacetoxiborhydride |
| spellingShingle | E. Yu. Osipova A. A. Simenel A. N. Rodionov V. V. Kachala K. Ya. Zherebker The preparation of 1-(β-naphthyl)-3-ferrocenylpyrazole-4-carbaldehyde and syntheses on the base of it Тонкие химические технологии acetylferrocene vilsmeier-haack reagent pyrazoles reductive amination triacetoxiborhydride |
| title | The preparation of 1-(β-naphthyl)-3-ferrocenylpyrazole-4-carbaldehyde and syntheses on the base of it |
| title_full | The preparation of 1-(β-naphthyl)-3-ferrocenylpyrazole-4-carbaldehyde and syntheses on the base of it |
| title_fullStr | The preparation of 1-(β-naphthyl)-3-ferrocenylpyrazole-4-carbaldehyde and syntheses on the base of it |
| title_full_unstemmed | The preparation of 1-(β-naphthyl)-3-ferrocenylpyrazole-4-carbaldehyde and syntheses on the base of it |
| title_short | The preparation of 1-(β-naphthyl)-3-ferrocenylpyrazole-4-carbaldehyde and syntheses on the base of it |
| title_sort | preparation of 1 β naphthyl 3 ferrocenylpyrazole 4 carbaldehyde and syntheses on the base of it |
| topic | acetylferrocene vilsmeier-haack reagent pyrazoles reductive amination triacetoxiborhydride |
| url | https://www.finechem-mirea.ru/jour/article/view/1113 |
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