Microwave assisted synthesis of 2,6-diaryl-4-piperidones and 2,4,6,8-tetraaryl-3,7-diazabicyclo[3.3.1]nonan-9-ones

One pot, three-component synthesis of 2,6-diaryl-4-piperidones and 2,4,6,8-tetraaryl-3,7-diazabicyclo[3.3.1]nonan-9-ones under microwave irradiation, was found to be efficient to afford good to excellent yields. This method has many advantages, which avoids the use of catalysts, accelerates the rate...

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Main Authors: G.L. Balaji, V. Vijayakumar, K. Rajesh
Format: Article
Language:English
Published: Elsevier 2016-11-01
Series:Arabian Journal of Chemistry
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S1878535211003121
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spelling doaj-39481c09726542f0b525a7cd9adf912d2020-11-25T01:57:55ZengElsevierArabian Journal of Chemistry1878-53522016-11-019S2S1101S110410.1016/j.arabjc.2011.12.011Microwave assisted synthesis of 2,6-diaryl-4-piperidones and 2,4,6,8-tetraaryl-3,7-diazabicyclo[3.3.1]nonan-9-onesG.L. BalajiV. VijayakumarK. RajeshOne pot, three-component synthesis of 2,6-diaryl-4-piperidones and 2,4,6,8-tetraaryl-3,7-diazabicyclo[3.3.1]nonan-9-ones under microwave irradiation, was found to be efficient to afford good to excellent yields. This method has many advantages, which avoids the use of catalysts, accelerates the rate of reaction, high yields, methodological simplicity and eco-friendliness.http://www.sciencedirect.com/science/article/pii/S1878535211003121Microwave irradiation2,6-Diaryl-4-piperidinones2,4,6,8-Tetraaryl-3,7-diazabicyclo[3.3.1]nonan-9-ones
collection DOAJ
language English
format Article
sources DOAJ
author G.L. Balaji
V. Vijayakumar
K. Rajesh
spellingShingle G.L. Balaji
V. Vijayakumar
K. Rajesh
Microwave assisted synthesis of 2,6-diaryl-4-piperidones and 2,4,6,8-tetraaryl-3,7-diazabicyclo[3.3.1]nonan-9-ones
Arabian Journal of Chemistry
Microwave irradiation
2,6-Diaryl-4-piperidinones
2,4,6,8-Tetraaryl-3,7-diazabicyclo[3.3.1]nonan-9-ones
author_facet G.L. Balaji
V. Vijayakumar
K. Rajesh
author_sort G.L. Balaji
title Microwave assisted synthesis of 2,6-diaryl-4-piperidones and 2,4,6,8-tetraaryl-3,7-diazabicyclo[3.3.1]nonan-9-ones
title_short Microwave assisted synthesis of 2,6-diaryl-4-piperidones and 2,4,6,8-tetraaryl-3,7-diazabicyclo[3.3.1]nonan-9-ones
title_full Microwave assisted synthesis of 2,6-diaryl-4-piperidones and 2,4,6,8-tetraaryl-3,7-diazabicyclo[3.3.1]nonan-9-ones
title_fullStr Microwave assisted synthesis of 2,6-diaryl-4-piperidones and 2,4,6,8-tetraaryl-3,7-diazabicyclo[3.3.1]nonan-9-ones
title_full_unstemmed Microwave assisted synthesis of 2,6-diaryl-4-piperidones and 2,4,6,8-tetraaryl-3,7-diazabicyclo[3.3.1]nonan-9-ones
title_sort microwave assisted synthesis of 2,6-diaryl-4-piperidones and 2,4,6,8-tetraaryl-3,7-diazabicyclo[3.3.1]nonan-9-ones
publisher Elsevier
series Arabian Journal of Chemistry
issn 1878-5352
publishDate 2016-11-01
description One pot, three-component synthesis of 2,6-diaryl-4-piperidones and 2,4,6,8-tetraaryl-3,7-diazabicyclo[3.3.1]nonan-9-ones under microwave irradiation, was found to be efficient to afford good to excellent yields. This method has many advantages, which avoids the use of catalysts, accelerates the rate of reaction, high yields, methodological simplicity and eco-friendliness.
topic Microwave irradiation
2,6-Diaryl-4-piperidinones
2,4,6,8-Tetraaryl-3,7-diazabicyclo[3.3.1]nonan-9-ones
url http://www.sciencedirect.com/science/article/pii/S1878535211003121
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AT vvijayakumar microwaveassistedsynthesisof26diaryl4piperidonesand2468tetraaryl37diazabicyclo331nonan9ones
AT krajesh microwaveassistedsynthesisof26diaryl4piperidonesand2468tetraaryl37diazabicyclo331nonan9ones
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