Iodine-Mediated, Microwave-Assisted Synthesis of 1-Arylnaphthofurans via Cyclization of 1-(1′-Arylvinyl)-2-naphthols

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DC Field	Value	Language
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
Appears in Collections:	Department of Chemistry

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