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Organocatalytic Highly Enantioselective α-Arylation of β-Ketoesters
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Asymmetric Organocatalytic α-Arylation of Aldehydes
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Titelbild: Organocatalytic Highly Enantioselective α-Arylation of β-Ketoesters / Asymmetric Organocatalytic α-Arylation of Aldehydes (Angew. Chem. 29/2007)
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Asymmetric Organocatalytic α-Arylation of Aldehydes
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Cover Picture: Organocatalytic Highly Enantioselective α-Arylation of β-Ketoesters / Asymmetric Organocatalytic α-Arylation of Aldehydes (Angew. Chem. Int. Ed. 29/2007)
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Thermodynamic properties of solid epoxide prepolymers
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Asymmetric 1,4-Addition of Oxazolones to Nitroalkenes by Bifunctional Cinchona Alkaloid Thiourea Organocatalysts: Synthesis of α,α-Disubstituted α-Amino Acids
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Corrigendum: Asymmetric Synthesis of 4-Amino-4H-Chromenes by Organocatalytic Oxa-Michael/Aza-Baylis–Hillman Tandem Reactions
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Organocatalytic Highly Enantioselective α-Arylation of β-Ketoesters
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Asymmetric Organocatalytic α-Arylation of Aldehydes
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ChemInform Abstract: Organocatalytic Asymmetric “anti-Michael” Reaction of β-Ketoesters
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ChemInform Abstract: Organocatalytic Asymmetric Vinylogous Addition to Quinones — Formation of Optically Active α-Aryl Ketones
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ChemInform Abstract: Asymmetric 1,4-Addition of Oxazolones to Nitroalkenes by Bifunctional Cinchona Alkaloid Thiourea Organocatalysts: Synthesis of α,α-Disubstituted α-Amino Acids
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ChemInform Abstract: Synthesis of 4-Hydroxy-4H-chromenes by Reaction of Salicylic Aldehydes with Alkynals Catalyzed by Silyl Prolinol Ethers
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