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 Field	Value	Language
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
Appears in Collections:	Department of Chemistry

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