A general strategy for diverse syntheses of anhydrolandomycinone, tetrangulol, and landomycinone

完整後設資料紀錄

DC 欄位	值	語言
dc.contributor.author	Sie, Cheng-Jhe	en_US
dc.contributor.author	Patteti, Venukumar	en_US
dc.contributor.author	Yang, Yi-Ru	en_US
dc.contributor.author	Mong, Kwok-Kong Tony	en_US
dc.date.accessioned	2018-08-21T05:53:19Z	-
dc.date.available	2018-08-21T05:53:19Z	-
dc.date.issued	2018-02-21	en_US
dc.identifier.issn	1359-7345	en_US
dc.identifier.uri	http://dx.doi.org/10.1039/c7cc09818a	en_US
dc.identifier.uri	http://hdl.handle.net/11536/144530	-
dc.description.abstract	A general synthetic strategy based on a protecting group-promoted CH arylation method was developed for total syntheses of anhydro-landomycinone (1), tetrangulol (2), and landomycinone (3) from the same set of starting materials.	en_US
dc.language.iso	en_US	en_US
dc.title	A general strategy for diverse syntheses of anhydrolandomycinone, tetrangulol, and landomycinone	en_US
dc.type	Article	en_US
dc.identifier.doi	10.1039/c7cc09818a	en_US
dc.identifier.journal	CHEMICAL COMMUNICATIONS	en_US
dc.citation.volume	54	en_US
dc.citation.spage	1885	en_US
dc.citation.epage	1888	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:000425192800017	en_US
顯示於類別：	期刊論文