The application of highly stereoselective aldol condensations to the synthesis of β-lactam antibiotics.
- 31 December 1985
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 26 (8) , 977-980
- https://doi.org/10.1016/s0040-4039(00)98490-9
Abstract
No abstract availableKeywords
This publication has 15 references indexed in Scilit:
- Conversion of .beta.-hydroxyglutarohydroxamates to carbapenem precursorsThe Journal of Organic Chemistry, 1983
- Enantioselective syntheses of 3-substituted 4-(alkoxycarbonyl)-2-azetidinones from malic acidThe Journal of Organic Chemistry, 1982
- Synthesis of Carbapenem AntibioticsHETEROCYCLES, 1982
- Silicon in synthesis: stabase adducts - a new primary amine protecting group: alkylation of ethyl glycinateTetrahedron Letters, 1981
- Synthesis of .beta.-lactams from substituted hydroxamic acidsJournal of the American Chemical Society, 1980
- Cyclofunctionalisation of unsaturated acids with benzeneselenenyl chlorideTetrahedron, 1980
- Stereospecific synthesis of .alpha.-amino-.beta.-hydroxy acidsThe Journal of Organic Chemistry, 1979
- A facile synthesis of substituted N-hydroxy-2-azetidinones. A biogenetic type .beta.-lactam synthesisJournal of the American Chemical Society, 1979
- PS-5, A new .BETA.-lactam antibiotic from Streptomyces.The Journal of Antibiotics, 1977
- Amino group protection in peptide synthesis. 4,5-Diphenyl-4-oxazolin-2-one groupThe Journal of Organic Chemistry, 1973