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http://dspace.bits-pilani.ac.in:8080/jspui/xmlui/handle/123456789/3166| Title: | An Unprecedented Pseudo-[3+2] Annulation between N-(4-Methoxyphenyl)aldimines and Aqueous Glutaraldehyde: Direct Synthesis of Pyrrole-2,4-dialdehydes |
| Authors: | Kumar, Indresh |
| Keywords: | Chemistry Synthesis Aqueous Glutaraldehyde |
| Issue Date: | 26-Apr-2017 |
| Publisher: | Wiley |
| 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. |
| URI: | https://chemistry-europe.onlinelibrary.wiley.com/doi/10.1002/ejoc.201700500 http://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/3166 |
| Appears in Collections: | Department of Chemistry |
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