Two-pot synthesis and photophysical studies of 1,6-disubstituted 5-aza-indoles from succinaldehyde and N-aryl propargylic-imines

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DC Field	Value	Language
dc.contributor.author	Kumar, Indresh	-
dc.date.accessioned	2024-09-12T04:34:54Z	-
dc.date.available	2024-09-12T04:34:54Z	-
dc.date.issued	2021	-
dc.identifier.uri	https://pubs.rsc.org/en/content/articlelanding/2021/ob/d1ob01949j	-
dc.identifier.uri	http://dspace.bits-pilani.ac.in:8080/jspui/xmlui/handle/123456789/15548	-
dc.description.abstract	A two-pot synthesis of 5-aza-indoles has been developed from aqueous succinaldehyde and N-aryl propargylic-imines. This overall protocol involves: (i) the metal-free [3 + 2] annulation of aqueous succinaldehyde and N-aryl propargylic-imines to access 2-alkynyl-pyrrole-3-aldehydes and (ii) Ag-catalyzed 6-endo-dig-cyclization to obtain substituted 5-aza-indoles in the second pot. The 5-aza-indoles showed engaging photophysical activities, and the practicality of this pot-economic gram-scale synthesis has been demonstrated.	en_US
dc.language.iso	en	en_US
dc.publisher	RSC	en_US
dc.subject	Synthesis	en_US
dc.subject	Chemistry	en_US
dc.subject	Succinaldehyde	en_US
dc.title	Two-pot synthesis and photophysical studies of 1,6-disubstituted 5-aza-indoles from succinaldehyde and N-aryl propargylic-imines	en_US
dc.type	Article	en_US
Appears in Collections:	Department of Chemistry

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