| 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 |
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