Synthesis of optically active penems
- 31 December 1981
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 22 (36) , 3485-3488
- https://doi.org/10.1016/s0040-4039(01)81938-9
Abstract
No abstract availableKeywords
This publication has 10 references indexed in Scilit:
- Deacylation of aromatic acetates. A new method of selective protection of the hydroxyl function.Tetrahedron Letters, 1981
- 7-Oxo-2-thia-1-azabicyclo[3.2.0]hept-3-ene, a revised structure for penems synthesized via oxidative addition mediated by copper(I)Tetrahedron Letters, 1980
- Synthesis of 2-oxo-bisnorpenicillin G estersTetrahedron Letters, 1980
- The penems, a new class of .beta.-lactam antibiotics. 5. Total synthesis of racemic 6-.alpha.-hydroxyethylpenemcarboxylic acidsJournal of the American Chemical Society, 1980
- Synthesis of penems and their antibacterial activities.The Journal of Antibiotics, 1980
- Stereoselective synthesis of 6β-substituted penicillanatesTetrahedron Letters, 1979
- The penems, a new class of .beta.-lactam antibiotics. 4. Syntheses of racemic and enantiomeric penem carboxylic acidsJournal of the American Chemical Society, 1979
- Penems. 1. Penem formation via a novel oxidative addition process mediated by copper(I)Journal of the American Chemical Society, 1979
- Aldol condensations of regiospecific penicillanate and cephalosporanate enolates. Hydroxyethylation at C-6 and C-7The Journal of Organic Chemistry, 1977
- Naturally-occurring .BETA.-lactamase inhibitors with antibacterial activity.The Journal of Antibiotics, 1976