3-Formylpyrroles from 3-Furfurylamines by Bromine Oxidation Reaction
| dc.citation.epage | 1326 | en_US |
| dc.citation.issue | 6B | en_US |
| dc.citation.spage | 1321 | en_US |
| dc.citation.volume | 57 | en_US |
| dc.citation.woscount | 1 | |
| dc.contributor.author | Harn, Piin-Jye | en_US |
| dc.contributor.author | Lin, Chu-Chung | en_US |
| dc.contributor.author | Wu, Hsien-Jen | en_US |
| dc.contributor.department | 應用化學系 | zh_TW |
| dc.contributor.department | Department of Applied Chemistry | en_US |
| dc.date.accessioned | 2014-12-08T15:38:20Z | |
| dc.date.available | 2014-12-08T15:38:20Z | |
| dc.date.issued | 2010-12-01 | en_US |
| dc.description.abstract | Oxidation of 3-furfurylamines 3a-e with bromine in acetone-water solution gave N-substituted 3-formylpyrroles 4a-e in good yields. A reaction mechanism via the Clauson-Kaas reaction followed by the cis-trans isomerization of the 2-ene-1,4-diones 13 and 14 was proposed to account for the formation of the pyrroles 4a-e. | en_US |
| dc.identifier.issn | 0009-4536 | en_US |
| dc.identifier.journal | JOURNAL OF THE CHINESE CHEMICAL SOCIETY | en_US |
| dc.identifier.uri | https://ir.lib.nycu.edu.tw/handle/11536/26259 | |
| dc.identifier.wosnumber | WOS:000288050400016 | |
| dc.language.iso | en_US | en_US |
| dc.subject | 3-Furfurylamines | en_US |
| dc.subject | 3-Formylpyrroles | en_US |
| dc.subject | Oxidation with bromine | en_US |
| dc.title | 3-Formylpyrroles from 3-Furfurylamines by Bromine Oxidation Reaction | en_US |
| dc.type | Article | en_US |
Files
License bundle
1 - 1 of 1
Loading...
- Name:
- license.txt
- Size:
- 1.71 KB
- Format:
- Item-specific license agreed to upon submission
- Description: