DSpace at EWHA: Gold-catalyzed intramolecular hydroalkoxylation/cyclization of conjugated dienyl alcohols

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DC Field	Value	Language
dc.contributor.author	류재상	*
dc.date.accessioned	2016-08-28T12:08:30Z	-
dc.date.available	2016-08-28T12:08:30Z	-
dc.date.issued	2012	*
dc.identifier.issn	0040-4020	*
dc.identifier.other	OAK-8866	*
dc.identifier.uri	https://dspace.ewha.ac.kr/handle/2015.oak/222719	-
dc.description.abstract	Catalytic intramolecular additions of hydroxyl groups to tethered conjugated dienes are described. The reactions proceed smoothly at 60 °C in the presence of 5 mol % of (PPh 3)AuCl/AgOTf as a catalyst. A broad range of structurally diverse conjugated dienes produce substituted tetrahydrofurans and tetrahydropyrans in good yields. This reaction represents an atom-economic route to construct five- and six-membered cyclic ethers. © 2012 Elsevier Ltd. All rights reserved.	*
dc.language	English	*
dc.title	Gold-catalyzed intramolecular hydroalkoxylation/cyclization of conjugated dienyl alcohols	*
dc.type	Article	*
dc.relation.issue	24	*
dc.relation.volume	68	*
dc.relation.index	SCI	*
dc.relation.index	SCIE	*
dc.relation.index	SCOPUS	*
dc.relation.startpage	4805	*
dc.relation.lastpage	4812	*
dc.relation.journaltitle	Tetrahedron	*
dc.identifier.doi	10.1016/j.tet.2012.03.120	*
dc.identifier.wosid	WOS:000304798800029	*
dc.identifier.scopusid	2-s2.0-84861221977	*
dc.author.google	Chandrasekhar B.	*
dc.author.google	Ryu J.-S.	*
dc.contributor.scopusid	류재상(36081118200)	*
dc.date.modifydate	20231120165709	*