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dc.contributor.author신승훈-
dc.date.accessioned2018-02-13T08:40:45Z-
dc.date.available2018-02-13T08:40:45Z-
dc.date.issued2011-06-
dc.identifier.citationChemistry - An Asian Journal, Vol.6 No.8 [2011], 1977-1981en_US
dc.identifier.issn1861-4728-
dc.identifier.urihttp://onlinelibrary.wiley.com/doi/10.1002/asia.201100159/abstract;jsessionid=53F0DDA59A08339FD8B21C6FA97E7526.f01t04-
dc.identifier.urihttp://hdl.handle.net/20.500.11754/37228-
dc.description.abstractAs strong as an aux: An electronically-tuned hydroxylamine functions as an excellent chiral auxiliary for [3+2] cycloaddition of the azomethine ylides generated in-situ from gold-catalyzed redox reaction of alkynyl nitrones.en_US
dc.description.sponsorshipFinancial support from the National Research Foundation of Korea (KRF-2009-0803) is gratefully acknowledged. This work was supported by Hi Seoul Science Humanities Fellowship (to H.S.Y.) from the Seoul Scholarship Foundation.en_US
dc.language.isoenen_US
dc.publisherWILEY-BLACKWELL, COMMERCE PLACE, 350 MAIN ST, MALDEN 02148, MA USAen_US
dc.subject[3+2] dipolar cycloadditionen_US
dc.subjectchiral auxiliariesen_US
dc.subjectgolden_US
dc.subjecthydroxylaminesen_US
dc.subjectylidesen_US
dc.titleAuxiliary-Controlled Asymmetric [3+2]-Dipolar Cycloaddition of Azomethine Ylides Generated from Au-Catalyzed Intramolecular Redox Reaction of Nitronyl Alkynesen_US
dc.typeArticleen_US
dc.relation.volume6-
dc.identifier.doi10.1002/asia.201100159-
dc.relation.page1977-1981-
dc.relation.journalCHEMISTRY-AN ASIAN JOURNAL-
dc.contributor.googleauthorJeong, Jaewon-
dc.contributor.googleauthorYeom, Hyun-Suk-
dc.contributor.googleauthorKwon, Ohyun-
dc.contributor.googleauthorShin, Seunghoon-
dc.relation.code2011215214-
dc.sector.campusS-
dc.sector.daehakCOLLEGE OF NATURAL SCIENCES[S]-
dc.sector.departmentDEPARTMENT OF CHEMISTRY-
dc.identifier.pidsshin-
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COLLEGE OF NATURAL SCIENCES[S](자연과학대학) > CHEMISTRY(화학과) > Articles
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