Synthesis of 3,11-dioxatetracyclo[6.3.0.0(2,6).0(5,9)]undecanes and 3,5,7-trioxapentacyclo[7.2.1.0(2,8).0(4,11).0(6,10)]dodecane

完整後設資料紀錄

DC 欄位	值	語言
dc.contributor.author	Lin, HC	en_US
dc.contributor.author	Wu, CY	en_US
dc.contributor.author	Wu, HJ	en_US
dc.date.accessioned	2014-12-08T15:01:16Z	-
dc.date.available	2014-12-08T15:01:16Z	-
dc.date.issued	1997-12-01	en_US
dc.identifier.issn	0009-4536	en_US
dc.identifier.uri	http://hdl.handle.net/11536/157	-
dc.description.abstract	The synthesis of 3,11-dioxatetracyclo[6.3.0.0(2,6).0(5,9)]undecanes has been accomplished from furans in a short sequence by iodine-induced cyclization reaction. The application of iodine-induced cyclization reaction for the synthesis of 3,5,7-trioxapentacyclo[7.2.1.0(2,8).0(4,11).0(6,10)]dodecane itself was also demonstrated.	en_US
dc.language.iso	en_US	en_US
dc.subject	3,11-dioxatetracyclo[6.3.0.0(2,6).0(5,9)]undecanes	en_US
dc.subject	3,5,7-trioxapentacyclo[7.2.1.0(2,8).0(4,11).0(6,10)]dodecane	en_US
dc.subject	iodine-induced cyclization	en_US
dc.title	Synthesis of 3,11-dioxatetracyclo[6.3.0.0(2,6).0(5,9)]undecanes and 3,5,7-trioxapentacyclo[7.2.1.0(2,8).0(4,11).0(6,10)]dodecane	en_US
dc.type	Article	en_US
dc.identifier.journal	JOURNAL OF THE CHINESE CHEMICAL SOCIETY	en_US
dc.citation.volume	44	en_US
dc.citation.issue	6	en_US
dc.citation.spage	609	en_US
dc.citation.epage	616	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:000071324900010	-
dc.citation.woscount	13	-
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