The asymmetric synthesis of β-lactam antibiotics -II. The first enantioselective synthesis of the carbacephalosporin nucleus.
- 1 January 1985
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 26 (32) , 3787-3790
- https://doi.org/10.1016/s0040-4039(00)89251-5
Abstract
No abstract availableKeywords
This publication has 11 references indexed in Scilit:
- Synthesis of methyl 3,5,9,11,13-pentaoxotetradecanoate, a "skipped" heptaketide, via ozonolysis of a hydroaromatic systemThe Journal of Organic Chemistry, 1985
- A simple synthesis of (±)-1-carbacephem derivativesTetrahedron Letters, 1983
- Titanate-Mediated Transesterifications with Functionalized SubstratesSynthesis, 1982
- Synthesis of 1-carbacephem derivatives.CHEMICAL & PHARMACEUTICAL BULLETIN, 1980
- Total synthesis of (−) homothienamycinTetrahedron Letters, 1980
- Trimethylsilyl as a Sulfur-Protecting Group; A New Convenient Preparation ofN-Protected 2-AminoethanethiolsSynthesis, 1980
- A Convenient Method for the Control of Selective Ozonizations of OlefinsSynthesis, 1980
- Nuclear analogs of β-lactam antibiotics. XI. Synthesis of 3-methyl-7-β-(phenoxyacetamido)-Δ3-desthiocephem-4-carboxylic acidCanadian Journal of Chemistry, 1979
- Total synthesis of (.+-.)-1-carbacefoxitin and -cefamandole and (.+-.)-1-oxacefamandoleJournal of Medicinal Chemistry, 1977
- Total synthesis of .beta.-lactam antibiotics. VIII. Stereospecific total synthesis of (+-)-1-carbacephalothinJournal of the American Chemical Society, 1974