REDUCTIVE REARRANGEMENT OF 5-NITROBICYCLO[2.2.1]HEPT-2-ENES - FORMATION OF 3-ARYLPYRIDINES

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DC Field	Value	Language
dc.contributor.author	HO, TL	en_US
dc.contributor.author	LIAO, PY	en_US
dc.date.accessioned	2014-12-08T15:04:02Z	-
dc.date.available	2014-12-08T15:04:02Z	-
dc.date.issued	1994-04-04	en_US
dc.identifier.issn	0040-4039	en_US
dc.identifier.uri	http://dx.doi.org/10.1016/S0040-4039(00)76799-2	en_US
dc.identifier.uri	http://hdl.handle.net/11536/2539	-
dc.description.abstract	Treatment of 6-aryl-5-nitrobicyclo[2.2.1]hept-2-enes with tin(II) chloride in refluxing THF or dioxane gave 3-arylpyridines via a deep-seated rearrangement.	en_US
dc.language.iso	en_US	en_US
dc.title	REDUCTIVE REARRANGEMENT OF 5-NITROBICYCLO[2.2.1]HEPT-2-ENES - FORMATION OF 3-ARYLPYRIDINES	en_US
dc.type	Article	en_US
dc.identifier.doi	10.1016/S0040-4039(00)76799-2	en_US
dc.identifier.journal	TETRAHEDRON LETTERS	en_US
dc.citation.volume	35	en_US
dc.citation.issue	14	en_US
dc.citation.spage	2211	en_US
dc.citation.epage	2212	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:A1994NE62100027	-
dc.citation.woscount	1	-
Appears in Collections:	Articles