| dc.contributor.author |
Kumar, Indresh |
|
| dc.date.accessioned |
2021-10-27T04:27:32Z |
|
| dc.date.available |
2021-10-27T04:27:32Z |
|
| dc.date.issued |
2017-04-26 |
|
| dc.identifier.uri |
https://chemistry-europe.onlinelibrary.wiley.com/doi/10.1002/ejoc.201700500 |
|
| dc.identifier.uri |
http://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/3166 |
|
| dc.description.abstract |
The 2-iodoxybenzoic acid (IBX)-mediated oxidative rearrangement of tetrahydropyridine intermediates, prepared through proline-catalyzed annulation between glutaraldehyde and imines, is explored as a means for the regioselective synthesis of pyrrole-2,4-dialdehydes. PMP = 4-MeOC6H4. |
en_US |
| dc.language.iso |
en |
en_US |
| dc.publisher |
Wiley |
en_US |
| dc.subject |
Chemistry |
en_US |
| dc.subject |
Synthesis |
en_US |
| dc.subject |
Aqueous Glutaraldehyde |
en_US |
| dc.title |
An Unprecedented Pseudo-[3+2] Annulation between N-(4-Methoxyphenyl)aldimines and Aqueous Glutaraldehyde: Direct Synthesis of Pyrrole-2,4-dialdehydes |
en_US |
| dc.type |
Article |
en_US |