| dc.contributor.author | Kumar, Dalip | |
| dc.date.accessioned | 2021-10-27T04:24:10Z | |
| dc.date.available | 2021-10-27T04:24:10Z | |
| dc.date.issued | 1998-12-10 | |
| dc.identifier.uri | https://www.sciencedirect.com/science/article/pii/S0040403998020590?via%3Dihub | |
| dc.identifier.uri | http://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/3106 | |
| dc.description.abstract | Easily accessible 2-aryl-1,2,3,4-tetrahydro-4-quinolones are readily oxidized to the corresponding 4-alkoxy-2-arylquinolines using a relatively safe hypervalent iodine reagent, [hydroxy (tosyloxy)iodo]benzene (HTIB), in high yields, thus providing a concise route to an important class of naturally occurring alkaloids. 2-Aryl-1,2,3,4-tetrahydro-4-quinolones are readily oxidized to the corresponding 4-alkoxy-2-arylquinolines by [hydroxy(tosyloxy)iodo]benzene(HTIB), thus providing a concise route to a class of naturally occurring alkaloids. | en_US |
| dc.language.iso | en | en_US |
| dc.publisher | Elsiever | en_US |
| dc.subject | Chemistry | en_US |
| dc.subject | Hypervalent | en_US |
| dc.title | Hypervalent iodine oxidation of 2-aryl-1,2,3,4-tetrahydro-4-quinolones: An expedient route to naturally occurring 4-alkoxy-2-arylquinolines | en_US |
| dc.type | Article | en_US |
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