Synthesis of isoxazolidin-5-ones via stereocontrolled Michael additions of benzylhydroxylamine to l-serine derived α,β-unsaturated esters
- 1 November 1998
- journal article
- Published by Elsevier in Tetrahedron: Asymmetry
- Vol. 9 (22) , 3945-3949
- https://doi.org/10.1016/s0957-4166(98)00412-1
Abstract
No abstract availableThis publication has 17 references indexed in Scilit:
- Asymmetric synthesis of an isoxazolidine nucleoside analog of thymine polyoxin CTetrahedron Letters, 1998
- New developments in the enantioselective synthesis of cyclopentyl carbocyclic nucleosidesTetrahedron, 1998
- Syntheses of isoxazolinyl and isoxazolidinyl nucleoside analoguesTetrahedron, 1998
- Heterocyclic Nucleosede Analogues by Cycloaddition Reactions of 1-Vinylthymine with 1,3-DepolesNucleosides and Nucleotides, 1998
- Oxidative Conversion of Isoxazolidines to IsoxazolinesThe Journal of Organic Chemistry, 1998
- Modified nucleosides from nitrones: a new and efficient stereoselective approach to isoxazolidinyl thymidine derivativesChemical Communications, 1998
- Structural modifications toward improved antisense oligonucleotidesPerspectives in Drug Discovery and Design, 1996
- Synthesis of Complex Nucleoside AntibioticsChemical Reviews, 1995
- Antiviral activities of isometric dideoxynucleosides of D- and L-related stereochemistryAntimicrobial Agents and Chemotherapy, 1995
- Nucleoside Analogues as Chemotherapeutic Agents: A ReviewNucleosides and Nucleotides, 1992