Synthesis of a Furanosyl-pyranone Derivative Related to the Tri-O-heterocyclic Core of Herbicidins

doi:10.1002/jccs.201100744

完整後設資料紀錄

DC 欄位	值	語言
dc.contributor.author	Hsu, Ching-Yun	en_US
dc.contributor.author	Lee, I-Chi	en_US
dc.contributor.author	Lico, Larry S.	en_US
dc.contributor.author	Uang, Biing-Jiun	en_US
dc.contributor.author	Hung, Shang-Cheng	en_US
dc.date.accessioned	2014-12-08T15:21:53Z	-
dc.date.available	2014-12-08T15:21:53Z	-
dc.date.issued	2012-03-01	en_US
dc.identifier.issn	0009-4536	en_US
dc.identifier.uri	http://dx.doi.org/10.1002/jccs.201100744	en_US
dc.identifier.uri	http://hdl.handle.net/11536/15577	-
dc.description.abstract	A new compound that is structurally related to the undecose ring structure of herbicidins has been prepared. The synthesis of this novel furanosyl-pyranone derivative was made possible through the regioselective reductive ring-opening of a 3,5-O-benzylidene-D-xylofuranose and the hetero-Diels-Alder reaction of an aldehyde and a Danishefsky-type diene. The highly functionalized pyranone derivative can be a useful precursor for the synthesis of herbicidins.	en_US
dc.language.iso	en_US	en_US
dc.subject	Benzylidene acetal	en_US
dc.subject	Cycloaddition	en_US
dc.subject	Danishefsky-type diene	en_US
dc.subject	Herbicidins	en_US
dc.subject	Regioselectivity	en_US
dc.title	Synthesis of a Furanosyl-pyranone Derivative Related to the Tri-O-heterocyclic Core of Herbicidins	en_US
dc.type	Article	en_US
dc.identifier.doi	10.1002/jccs.201100744	en_US
dc.identifier.journal	JOURNAL OF THE CHINESE CHEMICAL SOCIETY	en_US
dc.citation.volume	59	en_US
dc.citation.issue	3	en_US
dc.citation.spage	421	en_US
dc.citation.epage	425	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:000301092800023	-
dc.citation.woscount	0	-
顯示於類別：	期刊論文

文件中的檔案：

000301092800023.pdf

若為 zip 檔案，請下載檔案解壓縮後，用瀏覽器開啟資料夾中的 index.html 瀏覽全文。