Elaboration of the side chain of α-amino acids by palladium-catalysed stille couplings
- 1 March 1994
- journal article
- Published by Elsevier in Tetrahedron
- Vol. 50 (10) , 3213-3234
- https://doi.org/10.1016/s0040-4020(01)81118-2
Abstract
No abstract availableThis publication has 39 references indexed in Scilit:
- Double asymmetric synthesis: Palladium chiral complexes in the alkylation of chiral schiff bases derived from glycine.Tetrahedron Letters, 1990
- The stereoselective synthesis of .alpha.-amino acids by phase-transfer catalysisJournal of the American Chemical Society, 1989
- Synthesis of γ,δ,-unsaturated α-amino acids from allylsilanes and glycidyl cation equivalentsTetrahedron, 1989
- Asymmetric synthesis of α-amino acids: Comparison of enolate vs. cation functionalization of N-BOC-5, 6-diphenyl-2,3,5,6-tetrahydro-4h-1,4-oxazin-2-onesTetrahedron Letters, 1988
- Selective modification of glycine residues in dipeptidesTetrahedron Letters, 1988
- Reactions of a glycidyl radical equivalent with 2-functionalised allyl stannanesJournal of the Chemical Society, Chemical Communications, 1988
- Studies on the reaction of α-imino esters with organometallic compoundsTetrahedron, 1987
- Probing the active sites of aspartate: 2-oxoglutarate aminotransferases from Trichomonas vaginalis and pig heart cytoplasm using substrate analoguesComparative Biochemistry and Physiology Part B: Comparative Biochemistry, 1987
- Suicide substrates: mechanism-based enzyme inactivatorsTetrahedron, 1982
- Asymmetric Syntheses via Heterocyclic Intermediates; XII1. Enantioselective Synthesis of (R)-α-Amino Acids using tert-Leucine as Chiral Auxiliary ReagentSynthesis, 1982