Enantioselective synthesis of 4-substituted phenylalanines by cross-coupling reactions
- 8 January 1999
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 40 (2) , 213-216
- https://doi.org/10.1016/s0040-4039(98)02272-2
Abstract
No abstract availableThis publication has 9 references indexed in Scilit:
- Synthesis of 4-substituted phenylalanines by cross-coupling reactions: Extension of the methodology to aryl chloridesTetrahedron Letters, 1998
- Synthesis of 4-substituted phenylalanine derivatives by cross-coupling reaction of p-boronophenylalaninesTetrahedron Letters, 1997
- Novel Palladium(0)-Catalyzed Coupling Reaction of Dialkoxyborane with Aryl Halides: Convenient Synthetic Route to ArylboronatesThe Journal of Organic Chemistry, 1997
- Synthesis of arylboronates via the palladium(0)-catalyzed cross-coupling reaction of tetra(alkoxo)diborons with aryl triflatesTetrahedron Letters, 1997
- Synthesis of 4-Borono-L-phenylalanineSynlett, 1996
- Palladium-Catalyzed Cross-Coupling Reactions of Organoboron CompoundsChemical Reviews, 1995
- Palladium(0)-Catalyzed Cross-Coupling Reaction of Alkoxydiboron with Haloarenes: A Direct Procedure for Arylboronic EstersThe Journal of Organic Chemistry, 1995
- Resolution and use in α-amino acid synthesis of imidazolidinone glycine derivativesTetrahedron, 1988
- Pluripotential amino acids I. ()--dihydroxyborylphenylalanine (-Bph) as a precursor of -Phe and -Tyr containing peptides; specific tritiation of -Phe-containing peptides at a final step in synthesisTetrahedron Letters, 1980