An improved entry to a key intermediate for thienamycin synthesis from methyl (R)-3-hydroxybutanoate via direct epimerization at C-3 on 2-azetidinone rings
- 31 December 1985
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 26 (38) , 4647-4648
- https://doi.org/10.1016/s0040-4039(00)98775-6
Abstract
No abstract availableKeywords
This publication has 7 references indexed in Scilit:
- Stereocontrolled total synthesis of the chiral building block (3S,4R)-3- [(R)-1-hydroxyethyl]-4-acetyloxy-azetidin-2-one: a useful synthon for the synthesis of (+)-thienamycin, carbapenems and penems.Tetrahedron Letters, 1985
- A SYNTHETIC APPROACH TO (+)-THIENAMYCIN FROM METHYL (R)-3-HYDROXYBUTANOATE. A NEW ENTRY TO (3R, 4R)-3-[(R)-1-HYDROXYETHYL]-4-ACETOXY-2-AZETIDINONEChemistry Letters, 1985
- Stereocontrolled synthesis of (+)-thienamycin from 3(R)-hydroxybutyric acidTetrahedron Letters, 1985
- A FACILE ENTRY TO 3-(1-HYDROXYETHYL)-2-AZETIDINONES FROM METHYL (R)-3-HYDROXYBUTANOATE BASED ON THE ESTER ENOLATE-ALDIMINE CONDENSATIONChemistry Letters, 1984
- N-Trimethylsilylimines: applications to the syntheses of .beta.-lactamsJournal of the American Chemical Society, 1984
- An efficient synthesis of 2-substituted-thio-6-hydroxyethyl-penem-3-carboxylic acids via 2-thioxopenamsTetrahedron, 1983
- Synthesis of Carbapenem AntibioticsHETEROCYCLES, 1982