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Synthesis of 5-unsubstituted dihydropyrimidinone-4-carboxylates from deep eutectic mixtures
A facile one-pot synthesis of 5-unsubstituted dihydropyrimidinones from β,γ-unsaturated ketoesters in low melting ʟ-(+)-tartaric acid–N,N-dimethylurea mixtures is reported. This solvent-free method is very general and provides easy access to 5-unsubstituted dihydropyrimidinone-4-carboxylate derivati...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Beilstein-Institut
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8965339/ https://www.ncbi.nlm.nih.gov/pubmed/35387381 http://dx.doi.org/10.3762/bjoc.18.37 |
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author | Gore, Sangram Baskaran, Sundarababu König, Burkhard |
author_facet | Gore, Sangram Baskaran, Sundarababu König, Burkhard |
author_sort | Gore, Sangram |
collection | PubMed |
description | A facile one-pot synthesis of 5-unsubstituted dihydropyrimidinones from β,γ-unsaturated ketoesters in low melting ʟ-(+)-tartaric acid–N,N-dimethylurea mixtures is reported. This solvent-free method is very general and provides easy access to 5-unsubstituted dihydropyrimidinone-4-carboxylate derivatives in good yields. |
format | Online Article Text |
id | pubmed-8965339 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Beilstein-Institut |
record_format | MEDLINE/PubMed |
spelling | pubmed-89653392022-04-05 Synthesis of 5-unsubstituted dihydropyrimidinone-4-carboxylates from deep eutectic mixtures Gore, Sangram Baskaran, Sundarababu König, Burkhard Beilstein J Org Chem Full Research Paper A facile one-pot synthesis of 5-unsubstituted dihydropyrimidinones from β,γ-unsaturated ketoesters in low melting ʟ-(+)-tartaric acid–N,N-dimethylurea mixtures is reported. This solvent-free method is very general and provides easy access to 5-unsubstituted dihydropyrimidinone-4-carboxylate derivatives in good yields. Beilstein-Institut 2022-03-22 /pmc/articles/PMC8965339/ /pubmed/35387381 http://dx.doi.org/10.3762/bjoc.18.37 Text en Copyright © 2022, Gore et al. https://creativecommons.org/licenses/by/4.0/This is an open access article licensed under the terms of the Beilstein-Institut Open Access License Agreement (https://www.beilstein-journals.org/bjoc/terms/terms), which is identical to the Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0 (https://creativecommons.org/licenses/by/4.0/) ). The reuse of material under this license requires that the author(s), source and license are credited. Third-party material in this article could be subject to other licenses (typically indicated in the credit line), and in this case, users are required to obtain permission from the license holder to reuse the material. |
spellingShingle | Full Research Paper Gore, Sangram Baskaran, Sundarababu König, Burkhard Synthesis of 5-unsubstituted dihydropyrimidinone-4-carboxylates from deep eutectic mixtures |
title | Synthesis of 5-unsubstituted dihydropyrimidinone-4-carboxylates from deep eutectic mixtures |
title_full | Synthesis of 5-unsubstituted dihydropyrimidinone-4-carboxylates from deep eutectic mixtures |
title_fullStr | Synthesis of 5-unsubstituted dihydropyrimidinone-4-carboxylates from deep eutectic mixtures |
title_full_unstemmed | Synthesis of 5-unsubstituted dihydropyrimidinone-4-carboxylates from deep eutectic mixtures |
title_short | Synthesis of 5-unsubstituted dihydropyrimidinone-4-carboxylates from deep eutectic mixtures |
title_sort | synthesis of 5-unsubstituted dihydropyrimidinone-4-carboxylates from deep eutectic mixtures |
topic | Full Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8965339/ https://www.ncbi.nlm.nih.gov/pubmed/35387381 http://dx.doi.org/10.3762/bjoc.18.37 |
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