Pyrrolidines bearing a quaternary α-stereogenic center. Part 2: Access to proline chimeras, stereoselective approach and mechanistic aspects
- 21 May 2000
- journal article
- research article
- Published by Elsevier in Tetrahedron Letters
- Vol. 41 (20) , 3843-3847
- https://doi.org/10.1016/s0040-4039(00)00505-0
Abstract
No abstract availableKeywords
This publication has 41 references indexed in Scilit:
- New Conformationally Restricted Phosphorus- and Sulfur-Containing Structure Mimetics of Glutamic Acid - Pro-Glu ChimerasSynthesis, 1999
- Synthesis of novel proline and ψ-lactam derivatives as non-peptide mimics of Somatostatin/Sandostatin®Tetrahedron, 1999
- cis- and trans-3-(3-Indolyl)proline Derivatives as Conformationally Restricted Analogues of TryptophanSynlett, 1999
- Synthesis and Binding Affinities of Novel Spirocyclic Lactam Peptidomimetics of SomatostatinChemistry Letters, 1998
- Asymmetric synthesis of 2,4-disubstituted pyrrolidinesTetrahedron Letters, 1998
- Design and synthesis of conformationally constrained amino acids as versatile scaffolds and peptide mimeticsTetrahedron, 1997
- Synthesis, molecular modeling, and biology of the 1-benzyl derivative of APDC-an apparent mGluR6 selective ligandBioorganic & Medicinal Chemistry Letters, 1997
- Regioselective Enolization and Alkylation of 4-Oxo-N-(9-phenylfluoren-9-yl)proline: Synthesis of Enantiopure Proline−Valine and Hydroxyproline−Valine ChimerasThe Journal of Organic Chemistry, 1996
- Gem-disubstituted amino-ether based substance p antagonistsBioorganic & Medicinal Chemistry Letters, 1994
- Design and synthesis of potential DNA cross-linking reagents based on the anthramycin class of minor groove binding compoundsThe Journal of Organic Chemistry, 1988