A one-pot, multicomponent reaction for the synthesis of novel 2-alkyl substituted 4-aminoimidazo[1,2-a][1,3,5]triazines
A highly selective, one-pot, three-component synthesis of novel 2-alkyl-substituted 4-aminoimidazo[1,2-a] [1,3,5]triazines has been developed. The scope of the method was explored in two dimensions, varying the structures of trialkyl orthoesters and 2-aminoimidazoles in their reactions with cyanam...
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Royal Society of Chemistry
2018
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Online Access: | http://eprints.sunway.edu.my/842/1/Tieknink%20One%20Pot%20multicomponent.pdf http://eprints.sunway.edu.my/842/ http://doi.org/10.1039/c8ra03703e |
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my.sunway.eprints.8422020-10-07T09:05:47Z http://eprints.sunway.edu.my/842/ A one-pot, multicomponent reaction for the synthesis of novel 2-alkyl substituted 4-aminoimidazo[1,2-a][1,3,5]triazines Lim, Felicia Phei Lin Tan, Lin Yuing Tiekink, Edward R. T. * Dolzhenko, Anton V QD Chemistry A highly selective, one-pot, three-component synthesis of novel 2-alkyl-substituted 4-aminoimidazo[1,2-a] [1,3,5]triazines has been developed. The scope of the method was explored in two dimensions, varying the structures of trialkyl orthoesters and 2-aminoimidazoles in their reactions with cyanamide. Conveniently performed under microwave irradiation, this method was also proved to be efficient under conventional heating. A library of 24 novel compounds was prepared in high purity using this multicomponent approach. Molecular and crystal structures of representative molecules were studied using X-ray crystallography. Royal Society of Chemistry 2018-06-12 Article PeerReviewed text en http://eprints.sunway.edu.my/842/1/Tieknink%20One%20Pot%20multicomponent.pdf Lim, Felicia Phei Lin and Tan, Lin Yuing and Tiekink, Edward R. T. * and Dolzhenko, Anton V (2018) A one-pot, multicomponent reaction for the synthesis of novel 2-alkyl substituted 4-aminoimidazo[1,2-a][1,3,5]triazines. RSC Advances, 8 (38). pp. 21495-21504. ISSN 2046-2069 http://doi.org/10.1039/c8ra03703e doi:10.1039/c8ra03703e |
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QD Chemistry Lim, Felicia Phei Lin Tan, Lin Yuing Tiekink, Edward R. T. * Dolzhenko, Anton V A one-pot, multicomponent reaction for the synthesis of novel 2-alkyl substituted 4-aminoimidazo[1,2-a][1,3,5]triazines |
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A highly selective, one-pot, three-component synthesis of novel 2-alkyl-substituted 4-aminoimidazo[1,2-a]
[1,3,5]triazines has been developed. The scope of the method was explored in two dimensions, varying the
structures of trialkyl orthoesters and 2-aminoimidazoles in their reactions with cyanamide. Conveniently
performed under microwave irradiation, this method was also proved to be efficient under conventional heating. A library of 24 novel compounds was prepared in high purity using this multicomponent approach. Molecular and crystal structures of representative molecules were studied using X-ray crystallography. |
format |
Article |
author |
Lim, Felicia Phei Lin Tan, Lin Yuing Tiekink, Edward R. T. * Dolzhenko, Anton V |
author_facet |
Lim, Felicia Phei Lin Tan, Lin Yuing Tiekink, Edward R. T. * Dolzhenko, Anton V |
author_sort |
Lim, Felicia Phei Lin |
title |
A one-pot, multicomponent reaction for the synthesis of novel 2-alkyl substituted 4-aminoimidazo[1,2-a][1,3,5]triazines |
title_short |
A one-pot, multicomponent reaction for the synthesis of novel 2-alkyl substituted 4-aminoimidazo[1,2-a][1,3,5]triazines |
title_full |
A one-pot, multicomponent reaction for the synthesis of novel 2-alkyl substituted 4-aminoimidazo[1,2-a][1,3,5]triazines |
title_fullStr |
A one-pot, multicomponent reaction for the synthesis of novel 2-alkyl substituted 4-aminoimidazo[1,2-a][1,3,5]triazines |
title_full_unstemmed |
A one-pot, multicomponent reaction for the synthesis of novel 2-alkyl substituted 4-aminoimidazo[1,2-a][1,3,5]triazines |
title_sort |
one-pot, multicomponent reaction for the synthesis of novel 2-alkyl substituted 4-aminoimidazo[1,2-a][1,3,5]triazines |
publisher |
Royal Society of Chemistry |
publishDate |
2018 |
url |
http://eprints.sunway.edu.my/842/1/Tieknink%20One%20Pot%20multicomponent.pdf http://eprints.sunway.edu.my/842/ http://doi.org/10.1039/c8ra03703e |
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1680323398464438272 |
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13.160551 |