Publication: Catalytic Michael reactions of ketoesters with a camphor-derived acrylate equivalent: stereoselective access to all-carbon quaternary centers
Date
Date
Date
2008
Journal Article
Published version
Abstract
Abstract
Abstract
A camphor-based alpha'-hydroxy enone reagent acts as a chiral acrylate equivalent in copper-catalyzed Michael reactions of beta-keto esters and affords products that possess all-carbon quaternary stereocenters of high enantiomeric purity.
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2 since deposited on 2009-01-19
Acq. date: 2025-11-14
Views
179 since deposited on 2009-01-19
Acq. date: 2025-11-14
Additional indexing
Creators (Authors)
- Palomo, C
- Oiarbide, M
- Odriozola, J M
- Razkin, J
Volume
Volume
Volume
10
Number
Number
Number
13
Page range/Item number
Page range/Item number
Page range/Item number
2637
Page end
Page end
Page end
2640
Item Type
Item Type
Item Type
Journal Article
In collections
Dewey Decimal Classifikation
Dewey Decimal Classifikation
Dewey Decimal Classifikation
Language
Language
Language
English
Publication date
Publication date
Publication date
2008
Date available
Date available
Date available
2009-01-19
ISSN or e-ISSN
ISSN or e-ISSN
ISSN or e-ISSN
1523-7052
OA Status
OA Status
OA Status
Closed
Publisher DOI
Metrics
Downloads
2 since deposited on 2009-01-19
Acq. date: 2025-11-14
Views
179 since deposited on 2009-01-19
Acq. date: 2025-11-14
Closed
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Files
Files
Files available to download:1
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Linden_Catalytic_Michael_reactions_V.pdfview file PDF|1Download126.05 KB
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