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dc.contributor.author윤소원-
dc.date.accessioned2018-02-07T05:15:04Z-
dc.date.available2018-02-07T05:15:04Z-
dc.date.issued2011-07-
dc.identifier.citationEUROPEAN JOURNAL OF ORGANIC CHEMISTRY; JUL 2011, 20-21, p3904-p3910, 7p.en_US
dc.identifier.issn1434-193X-
dc.identifier.issn1099-0690-
dc.identifier.urihttp://onlinelibrary.wiley.com/doi/10.1002/ejoc.201100113/abstract-
dc.identifier.urihttp://hdl.handle.net/20.500.11754/35839-
dc.description.abstractA Au-I-catalyzed intramolecular cyclization reaction of 2-alkenylphenyl carbonyl compounds to afford a variety of indene, indenol, and indanone ring systems was developed. In this process, Au-I serves to activate the carbonyl group of beta-keto esters, aldehydes, and ketones, preferentially exhibiting oxophilicity in the presence of C-C multiple bonds. Furthermore, beta-keto esters could participate as the electrophilic partner in reactions with carbon nucleophile such as alkenes.en_US
dc.description.sponsorshipThis work was supported by the Mid-Career Researcher Program (No. R01-2009-008-3940) and Basic Science Research Program (Nos. 2010-0017149 and 2010-0007737) through the National Research Foundation of Korea (NRF) grant funded by the Ministry of Education, Science and Technology (MEST). A.R.J. is grateful for 2009 NRF Post-doctoral Fellowship Program for Foreign Researchers (No. K20802001473-10B120004500). We gratefully acknowledge Professor Juyoung Yoon (Department of Chemistry and Nano Science, Ewha Womans University) for his generous support. We also thank Dr. Ji-Eun Lee (Central Instrument Facility, Gyeongsang National University) for X-ray crystallographic analysis and Mr. Byung Seok Kim for assistance with spectroscopic data collection and analysis.en_US
dc.language.isoenen_US
dc.publisherWILEY-V C H VERLAG GMBH, POSTFACH 101161, 69451 WEINHEIM, GERMANYen_US
dc.subjectGolden_US
dc.subjectCyclizationen_US
dc.subjectCarbonyl compoundsen_US
dc.subjectAlkenesen_US
dc.subjectFused-ring systemsen_US
dc.titleAu-I-Catalyzed Intramolecular Cyclization of 2-Alkenylphenyl Carbonyl Compounds: Exploring the Oxophilic Lewis Acidity of Au-I Speciesen_US
dc.typeArticleen_US
dc.identifier.doi10.1002/ejoc.201100113-
dc.relation.page3904-3910-
dc.relation.journalEUROPEAN JOURNAL OF ORGANIC CHEMISTRY-
dc.contributor.googleauthorJagdale, Arun R.-
dc.contributor.googleauthorYoun, So Won-
dc.relation.code2011203042-
dc.sector.campusS-
dc.sector.daehakCOLLEGE OF NATURAL SCIENCES[S]-
dc.sector.departmentDEPARTMENT OF CHEMISTRY-
dc.identifier.pidsowony73-
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COLLEGE OF NATURAL SCIENCES[S](자연과학대학) > CHEMISTRY(화학과) > Articles
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