Thienamycin. A solution of the stereochemical problem
- 31 December 1979
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 20 (45) , 4359-4362
- https://doi.org/10.1016/s0040-4039(01)86588-6
Abstract
No abstract availableThis publication has 12 references indexed in Scilit:
- Penems. 1. Penem formation via a novel oxidative addition process mediated by copper(I)Journal of the American Chemical Society, 1979
- 7-[2-hydroxyethyl] cephalosporanic acid derivativesTetrahedron Letters, 1979
- Structures of three novel β-lactams isolated from Streptomyces clavuligerusJournal of the Chemical Society, Chemical Communications, 1979
- Synthesis of 7-oxo-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylates: the olivanic acid ring systemJournal of the Chemical Society, Chemical Communications, 1979
- Structure and absolute configuration of thienamycinJournal of the American Chemical Society, 1978
- Total synthesis of (.+-.)-thienamycinJournal of the American Chemical Society, 1978
- Aldol condensations of regiospecific penicillanate and cephalosporanate enolates. Hydroxyethylation at C-6 and C-7The Journal of Organic Chemistry, 1977
- Structure elucidation of MM 17880, a new fused β-lactam antibiotic isolated from Streptomyces olivaceus; a mild β-lactam degradation reactionJournal of the Chemical Society, Chemical Communications, 1977
- Structures of olivanic acid derivatives MM 4550 and MM 13902; two new, fused β-lactams isolated from Streptomyces olivaceusJournal of the Chemical Society, Chemical Communications, 1977
- Synthesis in the pyrrolizidine class of alkaloids. DL-SupinidineThe Journal of Organic Chemistry, 1975