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

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DC Field	Value	Language
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
Appears in Collections:	Department of Chemistry

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