Synthesis of dioxa-cages as a new probe for the stereochemistry of the bisadducts of p-quinone with cyclopentadiene and cyclohexadiene

dc.citation.epage	804	en_US
dc.citation.issue	6	en_US
dc.citation.spage	799	en_US
dc.citation.volume	45	en_US
dc.citation.woscount	6
dc.contributor.author	Yen, CH	en_US
dc.contributor.author	Tsai, SH	en_US
dc.contributor.author	Wu, HJ	en_US
dc.contributor.department	應用化學系	zh_TW
dc.contributor.department	Department of Applied Chemistry	en_US
dc.date.accessioned	2014-12-08T15:47:15Z
dc.date.available	2014-12-08T15:47:15Z
dc.date.issued	1998-12-01	en_US
dc.description.abstract	The synthesis of dioxa-cages via iodine-induced cyclization reaction can be used as a new method for the determination of the stereochemistry of the bisadducts of p-quinone with cyclopentadiene and cyclohexadiene. The bisadducts 2 and 8 were converted into the dioxa-cages 13a and 13b via a three-step sequence, respectively. The stereochemistry of 13a and 13b was determined on the basis of NOE experiments.	en_US
dc.identifier.issn	0009-4536	en_US
dc.identifier.journal	JOURNAL OF THE CHINESE CHEMICAL SOCIETY	en_US
dc.identifier.uri	https://ir.lib.nycu.edu.tw/handle/11536/31706
dc.identifier.wosnumber	WOS:000077788100014
dc.language.iso	en_US	en_US
dc.subject	synthesis of dioxa-cages	en_US
dc.subject	bisadducts of p-quinone with cyclopentadiene and cyclohexadiene	en_US
dc.title	Synthesis of dioxa-cages as a new probe for the stereochemistry of the bisadducts of p-quinone with cyclopentadiene and cyclohexadiene	en_US
dc.type	Article	en_US

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