完整後設資料紀錄
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dc.contributor.authorFukuyama, Takahideen_US
dc.contributor.authorOkada, Takumaen_US
dc.contributor.authorNakashima, Naoen_US
dc.contributor.authorRyu, Ilhyongen_US
dc.date.accessioned2019-12-13T01:12:16Z-
dc.date.available2019-12-13T01:12:16Z-
dc.date.issued2019-10-01en_US
dc.identifier.issn0018-019Xen_US
dc.identifier.urihttp://dx.doi.org/10.1002/hlca.201900186en_US
dc.identifier.urihttp://hdl.handle.net/11536/153144-
dc.description.abstractFormal [2+2+1] cycloaddition reaction involving acetylenes, aromatic imines, and CO was achieved by radical chain reaction, which gave five-membered unsaturated lactams in modest to good yields. When we used 5-chloropentyne, sequential carbonylation took place accompanied with double annulation events to give a cyclohexanone-fused lactam in excellent stereoselectivity.en_US
dc.language.isoen_USen_US
dc.subjectcycloadditionen_US
dc.subjectalkynesen_US
dc.subjectCOen_US
dc.subjectaromatic iminesen_US
dc.subjectlactamsen_US
dc.titleRadical Mediated Aza-Pauson-Khand Reaction of Acetylenes, Imines, and CO Leading to Five-Membered Unsaturated Lactamsen_US
dc.typeArticleen_US
dc.identifier.doi10.1002/hlca.201900186en_US
dc.identifier.journalHELVETICA CHIMICA ACTAen_US
dc.citation.volume102en_US
dc.citation.issue10en_US
dc.citation.spage0en_US
dc.citation.epage0en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000496451400002en_US
dc.citation.woscount0en_US
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