☆ 4.6 Article

Highly Enantioselective Decarboxylative Mannich Reaction of Malonic Acid Half Oxyesters with Cyclic Trifluoromethyl Ketimines: Synthesis of β-Amino Esters and Anti-HIV Drug DPC 083

CHEMISTRY-A EUROPEAN JOURNAL (2013)

Journal

CHEMISTRY-A EUROPEAN JOURNAL

Volume 19, Issue 47, Pages 15856-15860

Publisher

WILEY-V C H VERLAG GMBH

DOI: 10.1002/chem.201303307

Keywords

asymmetric catalysis; beta-amino esters; decarboxylative Mannich reaction; malonic acid half oxyesters; saccharide-derived amino-thioureas

Funding

National Natural Science Foundation of China
National Basic Research Program of China (973 Program) [2014CB745100]

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Highly Enantioselective Decarboxylative Mannich Reaction of Malonic Acid Half Oxyesters with Cyclic Trifluoromethyl Ketimines: Synthesis of β-Amino Esters and Anti-HIV Drug DPC 083

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CHEMISTRY-A EUROPEAN JOURNAL

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WILEY-V C H VERLAG GMBH

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Highly Enantioselective Decarboxylative Mannich Reaction of Malonic Acid Half Oxyesters with Cyclic Trifluoromethyl Ketimines: Synthesis of β-Amino Esters and Anti-HIV Drug DPC 083

Journal

CHEMISTRY-A EUROPEAN JOURNAL

Publisher

WILEY-V C H VERLAG GMBH

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