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Synthesis of new functionalized 3,7-diazabicyclo[3.3.1]nonanes by aminomethylation of the Guareschi imides

The aminomethylation of 4,4-dialkyl-2,6-dioxopiperidine-3,5-dicarbonitriles (Guareschi imides) was studied for the first time. When the Guareschi imides were treated with primary aliphatic amines and an excess of formaldehyde, 2,4-dioxo-3,7-diazabicyclo[3.3.1]nonane-1,5-dicarbonitriles were obtained...

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Главные авторы: Dotsenko, V. V., Доценко, В. В., Aksenov, N. A., Аксенов, Н. А., Aksenova, I. V., Аксенова, И. В.
Формат: Статья
Язык:English
Опубликовано: Elsevier Ltd 2018
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Online-ссылка:https://dspace.ncfu.ru:443/handle/20.500.12258/497
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spelling ir-20.500.12258-4972025-02-12T12:49:17Z Synthesis of new functionalized 3,7-diazabicyclo[3.3.1]nonanes by aminomethylation of the Guareschi imides Dotsenko, V. V. Доценко, В. В. Aksenov, N. A. Аксенов, Н. А. Aksenova, I. V. Аксенова, И. В. 2,6-Dioxopiperidine-3,5-dicarbonitriles 3,7-Diazabicyclo[3.3.1]nonanes Guareschi imides Mannich reaction The aminomethylation of 4,4-dialkyl-2,6-dioxopiperidine-3,5-dicarbonitriles (Guareschi imides) was studied for the first time. When the Guareschi imides were treated with primary aliphatic amines and an excess of formaldehyde, 2,4-dioxo-3,7-diazabicyclo[3.3.1]nonane-1,5-dicarbonitriles were obtained in varying yields (15–67%). The structure of 9,9-dimethyl-7-(2-methylpropyl)-2,4-dioxo-3,7-diazabicyclo[3.3.1]nonane-1,5-dicarbonitrile was studied by X-ray diffraction analysis 2018-06-07T09:57:18Z 2018-06-07T09:57:18Z 2017 Статья Khrustaleva, A.N., Frolov, K.A., Dotsenko, V.V., Aksenov, N.A., Aksenova, I.V., Krivokolysko, S.G. Synthesis of new functionalized 3,7-diazabicyclo[3.3.1]nonanes by aminomethylation of the Guareschi imides // Tetrahedron Letters. - 2018. - Volume 58. - Issue 50. - pp. 4663-4666. https://dspace.ncfu.ru:443/handle/20.500.12258/497 en Tetrahedron Letters application/pdf application/pdf Elsevier Ltd
institution СКФУ
collection Репозиторий
language English
topic 2,6-Dioxopiperidine-3,5-dicarbonitriles
3,7-Diazabicyclo[3.3.1]nonanes
Guareschi imides
Mannich reaction
spellingShingle 2,6-Dioxopiperidine-3,5-dicarbonitriles
3,7-Diazabicyclo[3.3.1]nonanes
Guareschi imides
Mannich reaction
Dotsenko, V. V.
Доценко, В. В.
Aksenov, N. A.
Аксенов, Н. А.
Aksenova, I. V.
Аксенова, И. В.
Synthesis of new functionalized 3,7-diazabicyclo[3.3.1]nonanes by aminomethylation of the Guareschi imides
description The aminomethylation of 4,4-dialkyl-2,6-dioxopiperidine-3,5-dicarbonitriles (Guareschi imides) was studied for the first time. When the Guareschi imides were treated with primary aliphatic amines and an excess of formaldehyde, 2,4-dioxo-3,7-diazabicyclo[3.3.1]nonane-1,5-dicarbonitriles were obtained in varying yields (15–67%). The structure of 9,9-dimethyl-7-(2-methylpropyl)-2,4-dioxo-3,7-diazabicyclo[3.3.1]nonane-1,5-dicarbonitrile was studied by X-ray diffraction analysis
format Статья
author Dotsenko, V. V.
Доценко, В. В.
Aksenov, N. A.
Аксенов, Н. А.
Aksenova, I. V.
Аксенова, И. В.
author_facet Dotsenko, V. V.
Доценко, В. В.
Aksenov, N. A.
Аксенов, Н. А.
Aksenova, I. V.
Аксенова, И. В.
author_sort Dotsenko, V. V.
title Synthesis of new functionalized 3,7-diazabicyclo[3.3.1]nonanes by aminomethylation of the Guareschi imides
title_short Synthesis of new functionalized 3,7-diazabicyclo[3.3.1]nonanes by aminomethylation of the Guareschi imides
title_full Synthesis of new functionalized 3,7-diazabicyclo[3.3.1]nonanes by aminomethylation of the Guareschi imides
title_fullStr Synthesis of new functionalized 3,7-diazabicyclo[3.3.1]nonanes by aminomethylation of the Guareschi imides
title_full_unstemmed Synthesis of new functionalized 3,7-diazabicyclo[3.3.1]nonanes by aminomethylation of the Guareschi imides
title_sort synthesis of new functionalized 3,7-diazabicyclo[3.3.1]nonanes by aminomethylation of the guareschi imides
publisher Elsevier Ltd
publishDate 2018
url https://dspace.ncfu.ru:443/handle/20.500.12258/497
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