Highly stereoselective free radical C-6-allylation of penams - synthesis of a noval β-lactamase inhibitor
- 1 January 1989
- journal article
- research article
- Published by Elsevier in Tetrahedron
- Vol. 45 (4) , 941-950
- https://doi.org/10.1016/0040-4020(89)80006-7
Abstract
No abstract availableThis publication has 42 references indexed in Scilit:
- Enantioselective Syntheses of Carbapenem AntibioticsHETEROCYCLES, 1987
- Penems: some recent advancesPublished by Walter de Gruyter GmbH ,1987
- A new synthetic strategy for the penems. Total synthesis of (5R,6S,8R)-6-(.alpha.-hydroxyethyl)-2-(hydroxymethyl)penem-3-carboxylic acidJournal of the American Chemical Society, 1985
- Stereocontrolled synthesis of an ene-carbapenem antibiotic (-)-asparenomycin CJournal of the American Chemical Society, 1983
- New .BETA.-lactam antibiotics, carpetimycins C and D.The Journal of Antibiotics, 1983
- Synthesis of New Orally Absorbed Penem Esters, Structurally Related to Thienamycin and CephamycinsHETEROCYCLES, 1983
- A new synthesis of penems, the oxalimide cyclization reactionJournal of the American Chemical Society, 1982
- Synthesis of Carbapenem AntibioticsHETEROCYCLES, 1982
- CARPETIMYCINS A AND B, NEW β-LACTAM ANTIBIOTICSThe Journal of Antibiotics, 1980
- Thienamycin, a new .BETA.-lactam antibiotic. I. Discovery, taxonomy, isolation and physical properties.The Journal of Antibiotics, 1979