| dc.contributor.author |
Kumar, Anil |
|
| dc.date.accessioned |
2021-10-17T13:56:14Z |
|
| dc.date.available |
2021-10-17T13:56:14Z |
|
| dc.date.issued |
2015 |
|
| dc.identifier.uri |
https://www.thieme-connect.com/products/ejournals/abstract/10.1055/s-0035-1560268 |
|
| dc.identifier.uri |
http://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/2856 |
|
| dc.description.abstract |
A metal-free, one-pot, iodine-mediated, microwave-assisted cyclization of 1-(1′-arylvinyl)-2-naphthols (ortho-vinylnaphthols) into 1-arylnaphthofurans is developed. The 1-arylnaphthofurans are isolated in good to excellent yields (65–90%) using two equivalents of iodine in acetonitrile. The reactions proceed via the formation of 1-(2-iodo-1-phenylvinyl)naphthalen-2-ols as intermediates. Overall, the protocol is convenient as the reactions occur smoothly without the requirement of a transition-metal catalyst. |
en_US |
| dc.language.iso |
en |
en_US |
| dc.publisher |
Thieme |
en_US |
| dc.subject |
Chemistry |
en_US |
| dc.subject |
Iodine-mediated |
en_US |
| dc.subject |
Microwave-assisted |
en_US |
| dc.subject |
Hydroarylation |
en_US |
| dc.subject |
1-arylnaphthofurans |
en_US |
| dc.subject |
one-pot reaction |
en_US |
| dc.title |
Iodine-Mediated, Microwave-Assisted Synthesis of 1-Arylnaphthofurans via Cyclization of 1-(1′-Arylvinyl)-2-naphthols |
en_US |
| dc.type |
Article |
en_US |