Hydroxy-Group-Facilitated Vinylic Iodination of ortho-Vinylnaphthols Using Molecular Iodine

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dc.contributor.authorKumar, Anil
dc.date.accessioned2021-10-14T13:13:03Z
dc.date.available2021-10-14T13:13:03Z
dc.date.issued2016
dc.description.abstractAn 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.identifier.urihttps://www.thieme-connect.com/products/ejournals/abstract/10.1055/s-0035-1560559
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/2842
dc.language.isoenen_US
dc.publisherThiemeen_US
dc.subjectChemistryen_US
dc.subjectVinylic Iodinationen_US
dc.subjectIodovinylnaphtholsen_US
dc.subjectMolecular Iodineen_US
dc.titleHydroxy-Group-Facilitated Vinylic Iodination of ortho-Vinylnaphthols Using Molecular Iodineen_US
dc.typeArticleen_US

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