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Au-I-Catalyzed Intramolecular Cyclization of 2-Alkenylphenyl Carbonyl Compounds: Exploring the Oxophilic Lewis Acidity of Au-I Species
- Authors
- Jagdale, Arun R.; Youn, So Won
- Issue Date
- Jul-2011
- Publisher
- WILEY-V C H VERLAG GMBH
- Keywords
- Gold; Cyclization; Carbonyl compounds; Alkenes; Fused-ring systems
- Citation
- EUROPEAN JOURNAL OF ORGANIC CHEMISTRY, v.2011, no.20-21, pp.3904 - 3910
- Indexed
- SCIE
SCOPUS
- Journal Title
- EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
- Volume
- 2011
- Number
- 20-21
- Start Page
- 3904
- End Page
- 3910
- ISSN
- 1434-193X
- Abstract
- A 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.
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Related Researcher
- Youn, So Won
- COLLEGE OF NATURAL SCIENCES (DEPARTMENT OF CHEMISTRY)