Iodine-induced cyclization reaction of endo-thioester substituted norbornenes followed by methylthio group rearrangement

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DC Field	Value	Language
dc.contributor.author	Wu, HJ	en_US
dc.contributor.author	Tsai, SH	en_US
dc.contributor.author	Chung, WS	en_US
dc.date.accessioned	2014-12-08T15:02:14Z	-
dc.date.available	2014-12-08T15:02:14Z	-
dc.date.issued	1996-11-04	en_US
dc.identifier.issn	0040-4039	en_US
dc.identifier.uri	http://dx.doi.org/10.1016/0040-4039(96)01869-2	en_US
dc.identifier.uri	http://hdl.handle.net/11536/933	-
dc.description.abstract	Treatment of the endo-thioester group substituted norbornenes 3a-3d with iodine in aqueous tetrahydrofuran at 25 degrees C gave the novel methylthio group rearranged lactonization products 4a-4d in 80% yields; iodolactonization reaction of 9 was applied to the synthesis of novel diacetal trioxa-cage compound 13. Copyright (C) 1996 Elsevier Science Ltd	en_US
dc.language.iso	en_US	en_US
dc.title	Iodine-induced cyclization reaction of endo-thioester substituted norbornenes followed by methylthio group rearrangement	en_US
dc.type	Article	en_US
dc.identifier.doi	10.1016/0040-4039(96)01869-2	en_US
dc.identifier.journal	TETRAHEDRON LETTERS	en_US
dc.citation.volume	37	en_US
dc.citation.issue	45	en_US
dc.citation.spage	8209	en_US
dc.citation.epage	8212	en_US
dc.contributor.department	應用化學系	zh_TW
dc.contributor.department	Department of Applied Chemistry	en_US
dc.identifier.wosnumber	WOS:A1996VR55300041	-
dc.citation.woscount	22	-
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