An Unprecedented Pseudo-[3+2] Annulation between N-(4-Methoxyphenyl)aldimines and Aqueous Glutaraldehyde: Direct Synthesis of Pyrrole-2,4-dialdehydes

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dc.contributor.authorKumar, Indresh
dc.date.accessioned2021-10-27T04:27:32Z
dc.date.available2021-10-27T04:27:32Z
dc.date.issued2017-04-26
dc.description.abstractThe 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.identifier.urihttps://chemistry-europe.onlinelibrary.wiley.com/doi/10.1002/ejoc.201700500
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/3166
dc.language.isoenen_US
dc.publisherWileyen_US
dc.subjectChemistryen_US
dc.subjectSynthesisen_US
dc.subjectAqueous Glutaraldehydeen_US
dc.titleAn Unprecedented Pseudo-[3+2] Annulation between N-(4-Methoxyphenyl)aldimines and Aqueous Glutaraldehyde: Direct Synthesis of Pyrrole-2,4-dialdehydesen_US
dc.typeArticleen_US

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