A facile synthesis of 3-substituted pipecolic acids, chimeric amino acids
- 1 July 1997
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 38 (29) , 5069-5072
- https://doi.org/10.1016/s0040-4039(97)01128-3
Abstract
No abstract availableThis publication has 13 references indexed in Scilit:
- Design of MHC class II (DR4) ligands using conformationally restricted imino acids at p3 and p5Bioorganic & Medicinal Chemistry Letters, 1996
- Convenient preparations of racemic and enantiopure methyl 6-oxopipecolateSynthetic Communications, 1996
- An efficient route to the α-methyl ester ofL-glutamic acid, and its conversion into cis-5-hydroxy-L-pipecolic acidChemical Communications, 1996
- A short enantioselective synthesis of pipecolic acidTetrahedron: Asymmetry, 1995
- Ac-[3- and 4-Alkylthioproline31]-CCK4 Analogs: Synthesis and Implications for the CCK-B Receptor-Bound ConformationJournal of Medicinal Chemistry, 1995
- Highly enantioselective synthesis of pipecolic acid derivatives via an asymmetric aza-Diels–Alder reactionJournal of the Chemical Society, Chemical Communications, 1994
- Competitive NMDA antagonist that base their activity on a unique conformational effectBioorganic & Medicinal Chemistry Letters, 1992
- An improved synthesis of homoproline and derivativesThe Journal of Organic Chemistry, 1990
- Evaluation and synthesis of amino-hydroxy isoxazoles and pyrazoles as potential glycine agonistsJournal of Medicinal Chemistry, 1989
- A new, highly efficient method for the conversion of alcohols to thiolesters and thiolsTetrahedron Letters, 1981