Palladium-Catalyzed Regio- and Stereoselective Hydrosulfonation of Propiolate Esters

doi:10.1055/s-0036-1588501

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DC 欄位	值	語言
dc.contributor.author	Raju, Selvam	en_US
dc.contributor.author	Annamalai, Pratheepkumar	en_US
dc.contributor.author	Chan, Fu-Wei	en_US
dc.contributor.author	Tseng, Po-Yen	en_US
dc.contributor.author	Chen, Po-Yen	en_US
dc.contributor.author	Kuo, Ting-Shen	en_US
dc.contributor.author	Chuang, Shih-Ching	en_US
dc.date.accessioned	2019-04-03T06:41:12Z	-
dc.date.available	2019-04-03T06:41:12Z	-
dc.date.issued	2017-11-01	en_US
dc.identifier.issn	0039-7881	en_US
dc.identifier.uri	http://dx.doi.org/10.1055/s-0036-1588501	en_US
dc.identifier.uri	http://hdl.handle.net/11536/144044	-
dc.description.abstract	An efficient palladium-catalyzed addition reaction of alkyland arylsulfonic acids to propiolate esters to yield alkenyl sulfonates is demonstrated. The formation of alkenyl sulfonates is highly regio- and stereoselective with favorable yields of up to 95%, and two of the alkenyl sulfonates are utilized for a Sonogashira cross-coupling reaction to produce (Z)-1,3-enynoates.	en_US
dc.language.iso	en_US	en_US
dc.subject	palladium	en_US
dc.subject	sulfonic acid	en_US
dc.subject	propiolate	en_US
dc.subject	regioselective	en_US
dc.subject	stereoselective	en_US
dc.subject	alkenyl sulfonate	en_US
dc.subject	Sonogashira cross-coupling	en_US
dc.title	Palladium-Catalyzed Regio- and Stereoselective Hydrosulfonation of Propiolate Esters	en_US
dc.type	Article	en_US
dc.identifier.doi	10.1055/s-0036-1588501	en_US
dc.identifier.journal	SYNTHESIS-STUTTGART	en_US
dc.citation.volume	49	en_US
dc.citation.issue	22	en_US
dc.citation.spage	5007	en_US
dc.citation.epage	5016	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:000414660900010	en_US
dc.citation.woscount	0	en_US
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