| dc.contributor.author | Kumar, Anil | |
| dc.date.accessioned | 2021-10-14T13:13:03Z | |
| dc.date.available | 2021-10-14T13:13:03Z | |
| dc.date.issued | 2016 | |
| dc.identifier.uri | https://www.thieme-connect.com/products/ejournals/abstract/10.1055/s-0035-1560559 | |
| dc.identifier.uri | http://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/2842 | |
| dc.description.abstract | An efficient and simple one-pot method for the iodination of ortho-vinylnaphthols using molecular iodine is disclosed. The reaction is believed to proceed through formation of quinone methide intermediate. The method tolerates different functional groups and provides corresponding ortho-iodovinylnaphthols in good to excellent yields. | en_US |
| dc.language.iso | en | en_US |
| dc.publisher | Thieme | en_US |
| dc.subject | Chemistry | en_US |
| dc.subject | Vinylic Iodination | en_US |
| dc.subject | Iodovinylnaphthols | en_US |
| dc.subject | Molecular Iodine | en_US |
| dc.title | Hydroxy-Group-Facilitated Vinylic Iodination of ortho-Vinylnaphthols Using Molecular Iodine | en_US |
| dc.type | Article | en_US |
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