Synthesis of α-amino acids. Schiff base of glycine methyl ester. A new and efficient prochiral nucleophile in palladium chiral catalytic allylation.
- 31 December 1986
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 27 (38), 4573-4576
- https://doi.org/10.1016/s0040-4039(00)85006-6
Abstract
No abstract availableThis publication has 17 references indexed in Scilit:
- Synthesis of α-aminoacids by catalytic palladium (O) alkylation of schiff basesTetrahedron Letters, 1986
- Modification of optically active ferrocenylphosphine ligands for palladium-catalyzed asymmetric allylic alkylationTetrahedron Letters, 1986
- A model for metal-templated catalytic asymmetric induction via .pi.-allyl fragmentsOrganometallics, 1985
- Asymmetric synthesis. Asymmetric catalytic allylation using palladium chiral phosphine complexesJournal of the American Chemical Society, 1985
- Organometallic catalysis in asymmetric synthesisPublished by Walter de Gruyter GmbH ,1983
- Palladium-catalyzed asymmetric cyclization of methyl (E)-oxo-9-phenoxy-7-nonenoate and its analogsTetrahedron Letters, 1982
- New chiral ligands designed for palladium-catalysed asymmetric allylic alkylationJournal of the Chemical Society, Chemical Communications, 1982
- Asymmetric catalytic allylic alkylationPublished by Walter de Gruyter GmbH ,1982
- Recent advances in asymmetric synthesisTetrahedron, 1979
- Asymmetric catalytic allylation of β-diketones or β-ketoesters with allylic ethers using a palladium-DIOP catalyst: A mechanistic studyJournal of Organometallic Chemistry, 1978