| dc.contributor.author | Kumar, Anil | |
| dc.date.accessioned | 2021-10-17T13:59:13Z | |
| dc.date.available | 2021-10-17T13:59:13Z | |
| dc.date.issued | 2013 | |
| dc.identifier.uri | https://pubs.acs.org/doi/abs/10.1021/ol4016354 | |
| dc.identifier.uri | http://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/2897 | |
| dc.description.abstract | A new strategy is reported for the synthesis of 6-aminoquinoline derivatives via a tandem Povarov reaction, dihydroquinoline oxidation, and imine reduction. These products allow access to symmetrical as well as unsymmetrical tetraarylpyrido[2,3-g]quinolines, potentially useful organic electronics | en_US |
| dc.language.iso | en | en_US |
| dc.publisher | ACS | en_US |
| dc.subject | Chemistry | en_US |
| dc.subject | Transfer reactions | en_US |
| dc.subject | Catalysts | en_US |
| dc.subject | Reaction products | en_US |
| dc.title | Povarov-Reductive Amination Cascade to Access 6-Aminoquinolines and Anthrazolines | en_US |
| dc.type | Article | en_US |
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