Detailed Information
Cited 21 time in 
Cited 24 time in 
Cited 24 time in
Metadata Downloads
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
- John Wiley & Sons Ltd.
- Keywords
- Gold; Cyclization; Carbonyl compounds; Alkenes; Fused-ring systems
- Citation
- European Journal of Organic Chemistry, v.2011, no.20-21, pp 3904 - 3910
- Pages
- 7
- Indexed
- SCI
SCIE
SCOPUS
- Journal Title
- European Journal of Organic Chemistry
- Volume
- 2011
- Number
- 20-21
- Start Page
- 3904
- End Page
- 3910
- ISSN
- 1434-193X
1099-0690
- 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.
- Files in This Item
- Go to Link
- Appears in
Collections - 서울 자연과학대학 > 서울 화학과 > 1. Journal Articles
Items in ScholarWorks are protected by copyright, with all rights reserved, unless otherwise indicated.
Related Researcher
- Youn, So Won
- COLLEGE OF NATURAL SCIENCES (DEPARTMENT OF CHEMISTRY)