Chloroperoxidase-mediated asymmetric epoxidation. Synthesis of (R)-dimethyl 2-methylaziridine-1,2-dicarboxylate—a potential α-methylamino acid synthon
- 13 November 1997
- journal article
- research article
- Published by Elsevier in Tetrahedron: Asymmetry
- Vol. 8 (21) , 3547-3550
- https://doi.org/10.1016/s0957-4166(97)00467-9
Abstract
No abstract availableKeywords
This publication has 18 references indexed in Scilit:
- Probing enzyme stereospecificity. Evaluation of β-Alkoxy-α-amino acids with two stereocenters as inhibitors of serine proteasesTetrahedron, 1995
- A New Asymmetric Synthesis of .alpha.-Methylcysteines via Chiral AziridinesThe Journal of Organic Chemistry, 1995
- Synthesis of α-amino acids by ring opening of aziridine-2-carboxylates with carbon nucleophilesTetrahedron Letters, 1995
- Total Synthesis of (-)-Thiangazole, a Naturally-Occurring HIV-1 InhibitorThe Journal of Organic Chemistry, 1994
- Revision of the stereostructure of mirabazole CTetrahedron Letters, 1994
- Total synthesis of mirabazole BTetrahedron Letters, 1994
- Total Synthesis of Didehydromirabazole A and Revision of StereostructureSynlett, 1994
- Synthesis of the thiazoline-based siderophore (S)-desferrithiocinTetrahedron, 1993
- Synthesis of functionalized amino acids by ring‐opening reactions of aliphatically substituted aziridine‐2‐carboxylic estersRecueil des Travaux Chimiques des Pays-Bas, 1992
- Non-proteinogenic amino acid synthesis. The β-anion derived from aspartic acid, and its application to α-amino acid synthesis.Tetrahedron, 1989