The generation of quatenary chiral centers through catalytic asymmetric alkylation of ketone enolates has been the subject of investigation in recent years. [1] The palladiumcatalyzed asymmetric allylic alkylation (AAA) of prochiral nucleophiles represents one such strategy for the creation of quate
✦ LIBER ✦
Palladium-Catalyzed Asymmetric Allylic Alkylation of α-Aryl Ketones
✍ Scribed by Barry M. Trost; Gretchen M. Schroeder; Jesper Kristensen
- Publisher
- John Wiley and Sons
- Year
- 2002
- Tongue
- English
- Weight
- 115 KB
- Volume
- 114
- Category
- Article
- ISSN
- 0044-8249
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📜 SIMILAR VOLUMES
Palladium-Catalyzed Asymmetric Allylic A
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Barry M. Trost; Gretchen M. Schroeder; Jesper Kristensen
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Article
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⚖ 115 KB
👁 1 views
Palladium-Catalyzed Asymmetric Allylic A
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⚖ 200 KB
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Palladium-Catalyzed Asymmetric Allylic α
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Barry M. Trost; Jiayi Xu
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⚖ 42 KB
Palladium-Catalyzed Asymmetric Allylic A
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Barry M. Trost; Gretchen M. Schroeder
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Article
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John Wiley and Sons
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## Abstract Palladium‐catalyzed asymmetric allylic alkylation of nonstabilized ketone enolates to generate quaternary centers has been achieved in excellent yield and enantioselectivity. Optimized conditions consist of performing the reaction in the presence of two equivalents of LDA as base, one e
Palladium-Catalyzed Asymmetric Allylic A
✍
Barry M. Trost; Gretchen M. Schroeder
📂
Article
📅
2006
🏛
John Wiley and Sons
⚖ 54 KB
👁 1 views
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.
Versatile Ligands for Palladium-Catalyze
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