Stereoselective synthesis of 1-β-methylcarbapenem
- 31 December 1987
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 28 (5) , 507-510
- https://doi.org/10.1016/s0040-4039(00)95767-8
Abstract
No abstract availableKeywords
This publication has 11 references indexed in Scilit:
- Lewis acid mediated condensation of chiral imide enolates. A general approach to the synthesis of chiral carbapenem precursorsJournal of the American Chemical Society, 1986
- Highly diastereoselective alkylation onto 4-acetoxy-2-azetidinones employing tin(II) enolates of 3-acyl C-4-chiral 1,3-thiazolidine-2-thionesJournal of the American Chemical Society, 1986
- Synthetic Carbapenem Antibiotics. I. 1-b-MethylcarbapenemHETEROCYCLES, 1984
- Recent Advances in Stereochemical Control: Multiple Asymmetric InductionHETEROCYCLES, 1984
- Synthetic approaches to thienamycin: Carbon-carbon bond formation at C-4 of azetidin-2-onesTetrahedron Letters, 1982
- Total synthesis of thienamycin: a new approach from aspartic acidTetrahedron Letters, 1982
- From Penicilin to Penem and Carbapenem. 1. Racemization of 6,6-Dibromo Secopenicillin, and Synthesis of 2-Oxo Penam DerivativeHETEROCYCLES, 1982
- Stereoselective Aldol CondensationsTopics in Stereochemistry, 1982
- Zirconium enolate as a new erythro-selective aldol condensation reagentTetrahedron Letters, 1980
- The Stereochemistry of the Ivanov and Reformatsky Reactions. IJournal of the American Chemical Society, 1957