Synthetic studies on carbapenem antibiotics from penicillins.II. regio- and stereoselective aldol reaction of a chiral azetidinone: a synthesis of optically active 6-epicarpetimycins
- 31 December 1984
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 25 (44) , 5075-5078
- https://doi.org/10.1016/s0040-4039(01)91123-2
Abstract
No abstract availableKeywords
This publication has 16 references indexed in Scilit:
- π-Allyltricarbonyliron lactone complexes in synthesis: application to the synthesis of the β-lactam antibiotic (+)-thienamycinJournal of the Chemical Society, Chemical Communications, 1984
- Synthetic Carbapenem Antibiotics. I. 1-b-MethylcarbapenemHETEROCYCLES, 1984
- Synthesis of 6-epithienamycinJournal of the Chemical Society, Chemical Communications, 1984
- Stereocontrolled synthesis of an ene-carbapenem antibiotic (-)-asparenomycin CJournal of the American Chemical Society, 1983
- Stereocontrolled synthesis of a cis-carbapenem antibiotic (-)-carpetimycin AJournal of the American Chemical Society, 1983
- Synthesis of 5,6-cis-carbapenems related to C-19393 H2Journal of the Chemical Society, Perkin Transactions 1, 1982
- Total synthesis of (±)-epithienamycins A and B [(±)-olivanic acids MM22380 and MM22382] and derivativesJournal of the Chemical Society, Perkin Transactions 1, 1981
- Thienamycin total synthesis. 1. Synthesis of azetidinone precursors of (.+-.)-thienamycin and its stereoisomersThe Journal of Organic Chemistry, 1980
- Radical-Induced Reductive Deamination of Amino Acid EstersSynthesis, 1980
- C‐Acylation under Virtually Neutral ConditionsAngewandte Chemie International Edition in English, 1979