On the stereochemical course of vinyloxyborane—imine condensation -the stereoselective formation of threo β-amino acid derivatives-
- 1 January 1986
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 27 (19) , 2153-2156
- https://doi.org/10.1016/s0040-4039(00)84473-1
Abstract
No abstract availableKeywords
This publication has 21 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
- An improved entry to a key intermediate for thienamycin synthesis from methyl ()-3-hydroxybutanoate via direct epimerization at C-3 on 2-azetidinone ringsTetrahedron Letters, 1985
- 3-(1′-hydroxyethyl)-2-azetidinones from 3-hydroxybutyrates and n-arylaldiminesTetrahedron Letters, 1985
- Stereocontrolled synthesis of (+)-thienamycin from 3(R)-hydroxybutyric acidTetrahedron Letters, 1985
- Stereoselective synthesis of 3-(1-Hydroxyethyl)-2-azetidinonesfrom 3-hydroxybutyratesTetrahedron Letters, 1984
- 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
- Aldol methodology: synthesis of versatile intermediates, 3-hydroxy-2-vinylcarbonyl compoundsJournal of the American Chemical Society, 1982
- Preparation of .beta.-lactams by the condensation of lithium ester enolates with aryl aldiminesThe Journal of Organic Chemistry, 1980
- The Reformatsky Reaction with BenzalanilineJournal of the American Chemical Society, 1943