Stereoselective Preparation of 2 Substituted Succinic Acid Dervatives Field of the Invention

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Abstract	Tetrahedron. Asymmetry vol. 6, No. 2, pp. 381-384, 1995; “Resolution of 2-Azol-1-ylsuccinic Esters by Enantiose lective Inclusion Methodology”, P. Zaderenko et al. Tetrahedron.: Asymmetry vol. 4, No. 5, pp. 783–792, 1993, “Enzymatic Resolution of 3-Substituted-4-oxoesters’, L. Blanco et al. Synlett, 1993, pp. 155-157, “Short and Efficient Large Scale Synthesis of (R)-2-Benzyluccinic Acid 4-4-(BOC amino)-1-piperidideMonoamide: N-Terminal Component of Renin Inhibitors of Asymmetric Hydrogenation”, H. Jendralla et al. Tetrahedron Letters, vol. 34, No. 28, pp. 4485–4488, 1993, “N-(Boc)-L-(2-Bromoallyl)-Glycine: A Versatile Interme diate for the Synthesis of Optically Active Unnatural Amino Acids', M. R. Leanna et al. Tetrahedron Letters, vol. 34, No. 28, pp. 4485–4488, 1993, “Enzyme-Catalyzed Synthesis of Optically Pure Beta-Sul fonamidopropionic Acids. Useful Starting Materials for P-3 Site Modified Renin Inhibitors”, H. Mazdiyasni et al. J. Chem. Soc. Perkin Trans, 1, 1990, pp. 1441–1445, “Asymmetric Synthesis of (R)-and (S)-4-(Substituted Benzyl)dihydrofuran-2(3H)-ones: An Application of the Ruthenium-binap+Complex-catalysed Asymmetric Hydrogenation of AlkylideneSuccinic Acids’, L. Shao et al.
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