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Pyrimidine Acyclo-C-Nucleosides by Ring Transformations of 2-Formyl-L-arabinal
The protected 2-formyl-L-arabinal 2 reacted with thiourea and cyanamide in the presence of sodium hydride to afford via ring transformations the 5-[1R,2S-1,2-bis(benzyloxy)-3-hydroxypropyl]-1,2-dihydropyrimidines 3 and 4, respectively. Similarly, treatment of 2 with 3-amino-2H-1,2,4-triazole yielded...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2005
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6147699/ https://www.ncbi.nlm.nih.gov/pubmed/18007353 http://dx.doi.org/10.3390/10080837 |
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author | Bari, Ahmed Feist, Holger Michalik, Manfred Peseke, Klaus |
author_facet | Bari, Ahmed Feist, Holger Michalik, Manfred Peseke, Klaus |
author_sort | Bari, Ahmed |
collection | PubMed |
description | The protected 2-formyl-L-arabinal 2 reacted with thiourea and cyanamide in the presence of sodium hydride to afford via ring transformations the 5-[1R,2S-1,2-bis(benzyloxy)-3-hydroxypropyl]-1,2-dihydropyrimidines 3 and 4, respectively. Similarly, treatment of 2 with 3-amino-2H-1,2,4-triazole yielded 6-[1R,2S-1,2-bis(benzyloxy)-3-hydroxypropyl][1,2,4]-triazolo[1,5-a]pyrimidine (5). |
format | Online Article Text |
id | pubmed-6147699 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2005 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-61476992018-11-19 Pyrimidine Acyclo-C-Nucleosides by Ring Transformations of 2-Formyl-L-arabinal Bari, Ahmed Feist, Holger Michalik, Manfred Peseke, Klaus Molecules Article The protected 2-formyl-L-arabinal 2 reacted with thiourea and cyanamide in the presence of sodium hydride to afford via ring transformations the 5-[1R,2S-1,2-bis(benzyloxy)-3-hydroxypropyl]-1,2-dihydropyrimidines 3 and 4, respectively. Similarly, treatment of 2 with 3-amino-2H-1,2,4-triazole yielded 6-[1R,2S-1,2-bis(benzyloxy)-3-hydroxypropyl][1,2,4]-triazolo[1,5-a]pyrimidine (5). MDPI 2005-08-31 /pmc/articles/PMC6147699/ /pubmed/18007353 http://dx.doi.org/10.3390/10080837 Text en © 2005 by MDPI (http://www.mdpi.org). Reproduction is permitted for non commercial purposes. |
spellingShingle | Article Bari, Ahmed Feist, Holger Michalik, Manfred Peseke, Klaus Pyrimidine Acyclo-C-Nucleosides by Ring Transformations of 2-Formyl-L-arabinal |
title | Pyrimidine Acyclo-C-Nucleosides by Ring Transformations of 2-Formyl-L-arabinal |
title_full | Pyrimidine Acyclo-C-Nucleosides by Ring Transformations of 2-Formyl-L-arabinal |
title_fullStr | Pyrimidine Acyclo-C-Nucleosides by Ring Transformations of 2-Formyl-L-arabinal |
title_full_unstemmed | Pyrimidine Acyclo-C-Nucleosides by Ring Transformations of 2-Formyl-L-arabinal |
title_short | Pyrimidine Acyclo-C-Nucleosides by Ring Transformations of 2-Formyl-L-arabinal |
title_sort | pyrimidine acyclo-c-nucleosides by ring transformations of 2-formyl-l-arabinal |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6147699/ https://www.ncbi.nlm.nih.gov/pubmed/18007353 http://dx.doi.org/10.3390/10080837 |
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