An Expedient Method for Resolution of 3-Amino-3-(3‘-pyridyl)propionic Acid and Related Compounds
- 26 October 2000
- journal article
- Published by American Chemical Society (ACS) in Organic Process Research & Development
- Vol. 5 (1), 23-27
- https://doi.org/10.1021/op990192m
Abstract
No abstract availableThis publication has 17 references indexed in Scilit:
- Potent, Orally Active GPIIb/IIIa Antagonists Containing a Nipecotic Acid Subunit. Structure−Activity Studies Leading to the Discovery of RWJ-53308Journal of Medicinal Chemistry, 1999
- The tert-Butanesulfinyl Group: An Ideal Chiral Directing Group and Boc-Surrogate for the Asymmetric Synthesis and Applications of β-Amino AcidsThe Journal of Organic Chemistry, 1998
- Solid-phase parallel synthesis applied to lead optimization: Discovery of potent analogues of the GPIIb/IIIa antagonist RWJ-50042Bioorganic & Medicinal Chemistry Letters, 1996
- An Efficient Synthesis of (S)-(+)-Ethyl β-Amino-3-pyridinepropanoate Using Enantiopure SulfiniminesThe Journal of Organic Chemistry, 1996
- Biocatalytic approach to enantiomerically pure β-amino acidsTetrahedron: Asymmetry, 1995
- 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 antagonistThe Journal of Organic Chemistry, 1993
- Nicotine analogs: synthesis of pyridylazetidinesThe Journal of Organic Chemistry, 1979
- Über die Kondensation von β‐Aryl‐β‐amino‐säuren mit δ‐Valero‐und ε‐Caprolactimäthern und die Cyclisierungsmöglichkeit der erhaltenen KondensationsprodukteJournal für Praktische Chemie, 1965
- The Synthesis of Possible Degradation Products of NicotineJournal of the American Pharmaceutical Association (Scientific ed.), 1954
- Researches on Pyrimidines. CXLIX. The Synthesis of Aryl Substituted Dihydrouracils and their Conversion to Uracil Derivatives1Journal of the American Chemical Society, 1936