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dc.contributor.authorRaju, Selvamen_US
dc.contributor.authorAnnamalai, Pratheepkumaren_US
dc.contributor.authorChan, Fu-Weien_US
dc.contributor.authorTseng, Po-Yenen_US
dc.contributor.authorChen, Po-Yenen_US
dc.contributor.authorKuo, Ting-Shenen_US
dc.contributor.authorChuang, Shih-Chingen_US
dc.date.accessioned2019-04-03T06:41:12Z-
dc.date.available2019-04-03T06:41:12Z-
dc.date.issued2017-11-01en_US
dc.identifier.issn0039-7881en_US
dc.identifier.urihttp://dx.doi.org/10.1055/s-0036-1588501en_US
dc.identifier.urihttp://hdl.handle.net/11536/144044-
dc.description.abstractAn 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.isoen_USen_US
dc.subjectpalladiumen_US
dc.subjectsulfonic aciden_US
dc.subjectpropiolateen_US
dc.subjectregioselectiveen_US
dc.subjectstereoselectiveen_US
dc.subjectalkenyl sulfonateen_US
dc.subjectSonogashira cross-couplingen_US
dc.titlePalladium-Catalyzed Regio- and Stereoselective Hydrosulfonation of Propiolate Estersen_US
dc.typeArticleen_US
dc.identifier.doi10.1055/s-0036-1588501en_US
dc.identifier.journalSYNTHESIS-STUTTGARTen_US
dc.citation.volume49en_US
dc.citation.issue22en_US
dc.citation.spage5007en_US
dc.citation.epage5016en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000414660900010en_US
dc.citation.woscount0en_US
Appears in Collections:Articles


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