N-acylimines as intermediates in reactions of α-substituted α-amino acids and dehyroamino acids
- 1 January 1975
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 16 (41) , 3579-3582
- https://doi.org/10.1016/s0040-4039(00)91373-x
Abstract
No abstract availableThis publication has 21 references indexed in Scilit:
- A Photochemical Route to N-Acyl IminesCanadian Journal of Chemistry, 1975
- Chemistry of dehydropeptides. Rearrangement of peptide isoxazolidinones derived from cycloserine.Tetrahedron Letters, 1974
- α,β-Unsaturated Carboxylic Acid Derivatives. VI. New Synthesis of N-Acyl-α-dehydroamino Acid EstersBulletin of the Chemical Society of Japan, 1974
- Chemistry of dehydropeptides. A rearrangement of an isothiazolone.Tetrahedron Letters, 1973
- Functionalization of C6(7) of penicillins and cephalosporins. One-step stereoselective synthesis of 7-.alpha.-methoxycephalosporin CJournal of the American Chemical Society, 1973
- Functionalization of penicillins at C-6 via N-acylimines for abstracting. 6-Hydroxy penicillin. Substituted penicillins and cephalosporns. VIIIThe Journal of Organic Chemistry, 1973
- Chemistry of dehydropeptides. Formation of isothiazolones and isothiazolidones from cysteinyl peptidesTetrahedron Letters, 1973
- Absolute configuration of (+)-trans-abscisic acid as determined by a quantitative application of the exciton chirality methodJournal of the American Chemical Society, 1973
- Dehydropeptides related to β-lactam antibiotics: a scheme for the biosynthesis of Penicillins and CephalosporinsJournal of the Chemical Society, Chemical Communications, 1973
- 2-azabicyclo[3.3.1]non-1-ene systems as reaction intermediatesTetrahedron Letters, 1972