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A highly stereoselective Michael addition to an alpha,beta-unsaturated ester as the crucial step in the synthesis of a novel beta-amino acid-containing fibrinogen receptor antagonist

A highly stereoselective Michael addition to an alpha,beta-unsaturated ester as the crucial step in the synthesis of a novel beta-amino acid-containing fibrinogen receptor antagonist

Journal of Organic Chemistry 58(27): 7948-7951

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Accession: 029660245

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DOI: 10.1021/jo00079a054

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