Pseudo-five-component stereoselective synthesis of highly functionalized 3-azabicyclo[3.3.1]nona-2,7-dienes
The reaction of aromatic aldehydes with malononitrile, ethyl or butyl cyanoacetate and acetylacetone in the presence of NaOH under mild conditions (EtOH, 25 degrees C) led to the formation of new series of (1S,5R,6R,9R)/(1R,5S,6S,9S)-2-amino-6,9-diaryl-7-acetyl-8-methyl-4-oxo-5-cyano-3-azabicyclo[3....
Kaydedildi:
Asıl Yazarlar: | , , , , , |
---|---|
Materyal Türü: | Статья |
Dil: | English |
Baskı/Yayın Bilgisi: |
MAIK NAUKA/INTERPERIODICA/SPRINGER
2021
|
Konular: | |
Online Erişim: | https://dspace.ncfu.ru/handle/20.500.12258/16377 |
Etiketler: |
Etiketle
Etiket eklenmemiş, İlk siz ekleyin!
|
id |
ir-20.500.12258-16377 |
---|---|
record_format |
dspace |
spelling |
ir-20.500.12258-163772021-07-05T14:13:28Z Pseudo-five-component stereoselective synthesis of highly functionalized 3-azabicyclo[3.3.1]nona-2,7-dienes Dotsenko, V. V. Доценко, В. В. Aksenov, N. A. Аксенов, Н. А. Aksenova, I. V. Аксенова, И. В. 3-azabicyclo[3; 3; 1]nonane 2-amino-4H-pyrans Methylene active nitriles Cyanoacetic ester Multicomponent reactions (MCRs) Cascade reactions The reaction of aromatic aldehydes with malononitrile, ethyl or butyl cyanoacetate and acetylacetone in the presence of NaOH under mild conditions (EtOH, 25 degrees C) led to the formation of new series of (1S,5R,6R,9R)/(1R,5S,6S,9S)-2-amino-6,9-diaryl-7-acetyl-8-methyl-4-oxo-5-cyano-3-azabicyclo[3.3.1]nona-2,7-diene-1-carboxylic acids esters. A plausible mechanism of the cascade reaction was proposed. 2021-07-02T12:17:03Z 2021-07-02T12:17:03Z 2021 Статья Ismiyev, AI; Dotsenko, VV; Aksenov, NA; Aksenova, IV; Magarramov, AM. Pseudo-five-component stereoselective synthesis of highly functionalized 3-azabicyclo[3.3.1]nona-2,7-dienes // RUSSIAN JOURNAL OF GENERAL CHEMISTRY. - 2021. - Том: 91. - Выпуск: 5. - Стр.: 758-767 http://hdl.handle.net/20.500.12258/16377 en Russian Journal of General Chemistry application/pdf application/pdf MAIK NAUKA/INTERPERIODICA/SPRINGER |
institution |
СКФУ |
collection |
Репозиторий |
language |
English |
topic |
3-azabicyclo[3; 3; 1]nonane 2-amino-4H-pyrans Methylene active nitriles Cyanoacetic ester Multicomponent reactions (MCRs) Cascade reactions |
spellingShingle |
3-azabicyclo[3; 3; 1]nonane 2-amino-4H-pyrans Methylene active nitriles Cyanoacetic ester Multicomponent reactions (MCRs) Cascade reactions Dotsenko, V. V. Доценко, В. В. Aksenov, N. A. Аксенов, Н. А. Aksenova, I. V. Аксенова, И. В. Pseudo-five-component stereoselective synthesis of highly functionalized 3-azabicyclo[3.3.1]nona-2,7-dienes |
description |
The reaction of aromatic aldehydes with malononitrile, ethyl or butyl cyanoacetate and acetylacetone in the presence of NaOH under mild conditions (EtOH, 25 degrees C) led to the formation of new series of (1S,5R,6R,9R)/(1R,5S,6S,9S)-2-amino-6,9-diaryl-7-acetyl-8-methyl-4-oxo-5-cyano-3-azabicyclo[3.3.1]nona-2,7-diene-1-carboxylic acids esters. A plausible mechanism of the cascade reaction was proposed. |
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 |
Pseudo-five-component stereoselective synthesis of highly functionalized 3-azabicyclo[3.3.1]nona-2,7-dienes |
title_short |
Pseudo-five-component stereoselective synthesis of highly functionalized 3-azabicyclo[3.3.1]nona-2,7-dienes |
title_full |
Pseudo-five-component stereoselective synthesis of highly functionalized 3-azabicyclo[3.3.1]nona-2,7-dienes |
title_fullStr |
Pseudo-five-component stereoselective synthesis of highly functionalized 3-azabicyclo[3.3.1]nona-2,7-dienes |
title_full_unstemmed |
Pseudo-five-component stereoselective synthesis of highly functionalized 3-azabicyclo[3.3.1]nona-2,7-dienes |
title_sort |
pseudo-five-component stereoselective synthesis of highly functionalized 3-azabicyclo[3.3.1]nona-2,7-dienes |
publisher |
MAIK NAUKA/INTERPERIODICA/SPRINGER |
publishDate |
2021 |
url |
https://dspace.ncfu.ru/handle/20.500.12258/16377 |
work_keys_str_mv |
AT dotsenkovv pseudofivecomponentstereoselectivesynthesisofhighlyfunctionalized3azabicyclo331nona27dienes AT docenkovv pseudofivecomponentstereoselectivesynthesisofhighlyfunctionalized3azabicyclo331nona27dienes AT aksenovna pseudofivecomponentstereoselectivesynthesisofhighlyfunctionalized3azabicyclo331nona27dienes AT aksenovna pseudofivecomponentstereoselectivesynthesisofhighlyfunctionalized3azabicyclo331nona27dienes AT aksenovaiv pseudofivecomponentstereoselectivesynthesisofhighlyfunctionalized3azabicyclo331nona27dienes AT aksenovaiv pseudofivecomponentstereoselectivesynthesisofhighlyfunctionalized3azabicyclo331nona27dienes |
_version_ |
1760599371347394560 |