A cascade A3 coupling strategy towards the regioselective synthesis of ?-carboline N-fused pyrrole derivatives with pyridine tethers
dc.contributor.author | Vaishali, None | |
dc.contributor.author | Malakar, Chandi C. | |
dc.contributor.author | Singh, Virender | |
dc.date.accessioned | 2024-01-21T10:33:05Z | |
dc.date.accessioned | 2024-08-13T11:16:18Z | |
dc.date.available | 2024-01-21T10:33:05Z | |
dc.date.available | 2024-08-13T11:16:18Z | |
dc.date.issued | 2022-12-01T00:00:00 | |
dc.description.abstract | A potential three component reaction strategy has been devised to generate nature inspired ?-carboline N-fused pyrroles containing pyridine tethers. These scaffolds were afforded in high yields via a one-pot cascade regioselective reaction of diverse Kumujian C, 2-aminopyridines and alkyne derivatives under Cu(ii)-catalysis. A library of 32 novel indolizino[8,7-b]indole derivatives with pyridine tethers has been developed. The current protocol offers excellent regioselectivity, high atom-economy and significant structural diversity. � 2023 The Royal Society of Chemistry. | en_US |
dc.identifier.doi | 10.1039/d2nj04620b | |
dc.identifier.issn | 11440546 | |
dc.identifier.uri | https://kr.cup.edu.in/handle/32116/3260 | |
dc.identifier.url | http://xlink.rsc.org/?DOI=D2NJ04620B | |
dc.language.iso | en_US | en_US |
dc.publisher | Royal Society of Chemistry | en_US |
dc.subject | Biomimetic processes | en_US |
dc.subject | Copper compounds | en_US |
dc.subject | Regioselectivity | en_US |
dc.subject | Scaffolds | en_US |
dc.subject | Synthesis (chemical) | en_US |
dc.subject | Tetherlines | en_US |
dc.subject | alkyne derivative | en_US |
dc.subject | beta carboline derivative | en_US |
dc.subject | copper | en_US |
dc.subject | indole derivative | en_US |
dc.subject | indolizino[8,7 b]indole derivative | en_US |
dc.subject | pyridine | en_US |
dc.subject | pyrrole derivative | en_US |
dc.subject | unclassified drug | en_US |
dc.subject | 2-Aminopyridine | en_US |
dc.subject | Fused pyrrole | en_US |
dc.subject | Higher yield | en_US |
dc.subject | One pot | en_US |
dc.subject | Pyrrole derivatives | en_US |
dc.subject | Reaction strategies | en_US |
dc.subject | Regioselective reactions | en_US |
dc.subject | Regioselective synthesis | en_US |
dc.subject | Three component reactions | en_US |
dc.subject | ?-carboline | en_US |
dc.subject | Article | en_US |
dc.subject | catalysis | en_US |
dc.subject | chemical structure | en_US |
dc.subject | cross coupling reaction | en_US |
dc.subject | economic aspect | en_US |
dc.subject | one pot synthesis | en_US |
dc.subject | regioselectivity | en_US |
dc.subject | synthesis | en_US |
dc.subject | Pyridine | en_US |
dc.title | A cascade A3 coupling strategy towards the regioselective synthesis of ?-carboline N-fused pyrrole derivatives with pyridine tethers | en_US |
dc.title.journal | New Journal of Chemistry | en_US |
dc.type | Article | en_US |
dc.type.accesstype | Closed Access | en_US |