Abstract
Palladium(II)-catalyzed carboxylation of chiral olefins 6a-d has been examined under various conditions. In the weak basic condition (K2CO3), 7a-d were obtained in good yields. Alternatively, in the strong basic condition, pyrrolidinones 8a-d were obtained resulting in excellent yields and with high diastereoselectivity.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Alkenes / chemistry
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Antineoplastic Agents / chemical synthesis*
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Antineoplastic Agents / pharmacology*
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Catalysis
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Chromatography, Gel
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Indicators and Reagents
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Magnetic Resonance Spectroscopy
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Palladium / chemistry
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Pyrrolidinones / chemical synthesis*
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Pyrrolidinones / pharmacology*
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Solvents
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Stereoisomerism
Substances
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Alkenes
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Antineoplastic Agents
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Indicators and Reagents
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Pyrrolidinones
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Solvents
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Palladium