Domino multicomponent intramolecular cyclization strategy for the multi functionalized Imidazo[1,2-a]pyrimidin-5(1h)-one derivatives
A microwave assisted novel domino synthetic approach to trifluoromethyl substituted imidazo[1,2-a]pyrimidin-5(1H)-one derivatives has been developed via a multi component cascade strategy in a single operation. The synthesized compounds can find application as structural components of biologically a...
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Pleiades Publishing
2021
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Online Access: | https://eprints.ums.edu.my/id/eprint/31189/1/Domino%20Multicomponent%20Intramolecular%20Cyclization%20Strategy%20for%20the%20Multi%20Functionalized%20Imidazo_ABSTRACT.pdf https://eprints.ums.edu.my/id/eprint/31189/ https://link.springer.com/article/10.1134/S1070363221060219 https://doi.org/10.1134/S1070363221060219 |
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my.ums.eprints.311892021-11-24T00:06:43Z https://eprints.ums.edu.my/id/eprint/31189/ Domino multicomponent intramolecular cyclization strategy for the multi functionalized Imidazo[1,2-a]pyrimidin-5(1h)-one derivatives P. R. Khan G. R. Alugubelli R. Sireesha K. Deepti Pasupuleti Visweswara Rao M. V. B. Rao QD241-441 Organic chemistry A microwave assisted novel domino synthetic approach to trifluoromethyl substituted imidazo[1,2-a]pyrimidin-5(1H)-one derivatives has been developed via a multi component cascade strategy in a single operation. The synthesized compounds can find application as structural components of biologically active compounds. Pleiades Publishing 2021 Article PeerReviewed text en https://eprints.ums.edu.my/id/eprint/31189/1/Domino%20Multicomponent%20Intramolecular%20Cyclization%20Strategy%20for%20the%20Multi%20Functionalized%20Imidazo_ABSTRACT.pdf P. R. Khan and G. R. Alugubelli and R. Sireesha and K. Deepti and Pasupuleti Visweswara Rao and M. V. B. Rao (2021) Domino multicomponent intramolecular cyclization strategy for the multi functionalized Imidazo[1,2-a]pyrimidin-5(1h)-one derivatives. Russian Journal of General Chemistry, 91. pp. 1123-1127. ISSN 1070-3632 (P-ISSN) , 1608-3350 (E-ISSN) https://link.springer.com/article/10.1134/S1070363221060219 https://doi.org/10.1134/S1070363221060219 |
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QD241-441 Organic chemistry P. R. Khan G. R. Alugubelli R. Sireesha K. Deepti Pasupuleti Visweswara Rao M. V. B. Rao Domino multicomponent intramolecular cyclization strategy for the multi functionalized Imidazo[1,2-a]pyrimidin-5(1h)-one derivatives |
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A microwave assisted novel domino synthetic approach to trifluoromethyl substituted imidazo[1,2-a]pyrimidin-5(1H)-one derivatives has been developed via a multi component cascade strategy in a single operation. The synthesized compounds can find application as structural components of biologically active compounds. |
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Article |
author |
P. R. Khan G. R. Alugubelli R. Sireesha K. Deepti Pasupuleti Visweswara Rao M. V. B. Rao |
author_facet |
P. R. Khan G. R. Alugubelli R. Sireesha K. Deepti Pasupuleti Visweswara Rao M. V. B. Rao |
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P. R. Khan |
title |
Domino multicomponent intramolecular cyclization strategy for the multi functionalized Imidazo[1,2-a]pyrimidin-5(1h)-one derivatives |
title_short |
Domino multicomponent intramolecular cyclization strategy for the multi functionalized Imidazo[1,2-a]pyrimidin-5(1h)-one derivatives |
title_full |
Domino multicomponent intramolecular cyclization strategy for the multi functionalized Imidazo[1,2-a]pyrimidin-5(1h)-one derivatives |
title_fullStr |
Domino multicomponent intramolecular cyclization strategy for the multi functionalized Imidazo[1,2-a]pyrimidin-5(1h)-one derivatives |
title_full_unstemmed |
Domino multicomponent intramolecular cyclization strategy for the multi functionalized Imidazo[1,2-a]pyrimidin-5(1h)-one derivatives |
title_sort |
domino multicomponent intramolecular cyclization strategy for the multi functionalized imidazo[1,2-a]pyrimidin-5(1h)-one derivatives |
publisher |
Pleiades Publishing |
publishDate |
2021 |
url |
https://eprints.ums.edu.my/id/eprint/31189/1/Domino%20Multicomponent%20Intramolecular%20Cyclization%20Strategy%20for%20the%20Multi%20Functionalized%20Imidazo_ABSTRACT.pdf https://eprints.ums.edu.my/id/eprint/31189/ https://link.springer.com/article/10.1134/S1070363221060219 https://doi.org/10.1134/S1070363221060219 |
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1760230862235893760 |
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13.211869 |