A novel hydride rearrangement of the acetal group of tetraacetal tetraoxa-cages mediated by Lewis acids

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DC Field	Value	Language
dc.contributor.author	Wu, HJ	en_US
dc.contributor.author	Chern, JH	en_US
dc.date.accessioned	2014-12-08T15:01:55Z	-
dc.date.available	2014-12-08T15:01:55Z	-
dc.date.issued	1997-03-21	en_US
dc.identifier.issn	1359-7345	en_US
dc.identifier.uri	http://dx.doi.org/10.1039/a607403k	en_US
dc.identifier.uri	http://hdl.handle.net/11536/662	-
dc.description.abstract	Treatment of tetraoxa-cages 1a-f with Lewis acids such as TlC4, AlCl3, BF3 . OEt(2) and MeSO(3)H in dichloromethane at 25 degrees C gives the rearrangement products 2a-f in 90% yields regioselectively and stereoselectively; a novel hydride rearrangement of the acetal group of tetraacetal tetraoxa-cages mediated by Lewis acids.	en_US
dc.language.iso	en_US	en_US
dc.title	A novel hydride rearrangement of the acetal group of tetraacetal tetraoxa-cages mediated by Lewis acids	en_US
dc.type	Article	en_US
dc.identifier.doi	10.1039/a607403k	en_US
dc.identifier.journal	CHEMICAL COMMUNICATIONS	en_US
dc.citation.volume		en_US
dc.citation.issue	6	en_US
dc.citation.spage	547	en_US
dc.citation.epage	548	en_US
dc.contributor.department	交大名義發表	zh_TW
dc.contributor.department	應用化學系	zh_TW
dc.contributor.department	National Chiao Tung University	en_US
dc.contributor.department	Department of Applied Chemistry	en_US
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