Cargando…
A Direct Route to 6,6’-Disubstituted-2,2’-Bipyridines by Double Diels-Alder/retro Diels-Alder Reaction of 5,5’-bi-1,2,4-Triazines†
Inverse electron demand Diels-Alder reaction of functionalized 5,5’-bi-1,2,4-triazines with bicyclo[2.2.1]hepta-2,5-diene in boiling p-cymene leads to a range of 6,6’-disubstituted-2,2’-bipyridines in good yield.
Autor principal: | |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2005
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6147683/ https://www.ncbi.nlm.nih.gov/pubmed/18007296 http://dx.doi.org/10.3390/10010274 |
_version_ | 1783356603721842688 |
---|---|
author | Branowska, Danuta |
author_facet | Branowska, Danuta |
author_sort | Branowska, Danuta |
collection | PubMed |
description | Inverse electron demand Diels-Alder reaction of functionalized 5,5’-bi-1,2,4-triazines with bicyclo[2.2.1]hepta-2,5-diene in boiling p-cymene leads to a range of 6,6’-disubstituted-2,2’-bipyridines in good yield. |
format | Online Article Text |
id | pubmed-6147683 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2005 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-61476832018-11-19 A Direct Route to 6,6’-Disubstituted-2,2’-Bipyridines by Double Diels-Alder/retro Diels-Alder Reaction of 5,5’-bi-1,2,4-Triazines† Branowska, Danuta Molecules Article Inverse electron demand Diels-Alder reaction of functionalized 5,5’-bi-1,2,4-triazines with bicyclo[2.2.1]hepta-2,5-diene in boiling p-cymene leads to a range of 6,6’-disubstituted-2,2’-bipyridines in good yield. MDPI 2005-01-31 /pmc/articles/PMC6147683/ /pubmed/18007296 http://dx.doi.org/10.3390/10010274 Text en © 2005 by MDPI (http://www.mdpi.org). Reproduction is permitted for noncommercial purposes. |
spellingShingle | Article Branowska, Danuta A Direct Route to 6,6’-Disubstituted-2,2’-Bipyridines by Double Diels-Alder/retro Diels-Alder Reaction of 5,5’-bi-1,2,4-Triazines† |
title | A Direct Route to 6,6’-Disubstituted-2,2’-Bipyridines by Double Diels-Alder/retro Diels-Alder Reaction of 5,5’-bi-1,2,4-Triazines† |
title_full | A Direct Route to 6,6’-Disubstituted-2,2’-Bipyridines by Double Diels-Alder/retro Diels-Alder Reaction of 5,5’-bi-1,2,4-Triazines† |
title_fullStr | A Direct Route to 6,6’-Disubstituted-2,2’-Bipyridines by Double Diels-Alder/retro Diels-Alder Reaction of 5,5’-bi-1,2,4-Triazines† |
title_full_unstemmed | A Direct Route to 6,6’-Disubstituted-2,2’-Bipyridines by Double Diels-Alder/retro Diels-Alder Reaction of 5,5’-bi-1,2,4-Triazines† |
title_short | A Direct Route to 6,6’-Disubstituted-2,2’-Bipyridines by Double Diels-Alder/retro Diels-Alder Reaction of 5,5’-bi-1,2,4-Triazines† |
title_sort | direct route to 6,6’-disubstituted-2,2’-bipyridines by double diels-alder/retro diels-alder reaction of 5,5’-bi-1,2,4-triazines† |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6147683/ https://www.ncbi.nlm.nih.gov/pubmed/18007296 http://dx.doi.org/10.3390/10010274 |
work_keys_str_mv | AT branowskadanuta adirectrouteto66disubstituted22bipyridinesbydoubledielsalderretrodielsalderreactionof55bi124triazines AT branowskadanuta directrouteto66disubstituted22bipyridinesbydoubledielsalderretrodielsalderreactionof55bi124triazines |