Stereoselective synthesis and absolute configuration of (1′R,3R,4R)-4-acetoxy-3-(2′,2′,2′-trifluoro-1′-hydroxyethyl)azetidin-2-one
- 30 January 1998
- journal article
- Published by Elsevier in Tetrahedron: Asymmetry
- Vol. 9 (2) , 285-292
- https://doi.org/10.1016/s0957-4166(97)00640-x
Abstract
No abstract availableKeywords
This publication has 13 references indexed in Scilit:
- Synthesis of 3-fluoro azetidinone by electrophilic fluorinationTetrahedron Letters, 1997
- Preparations of two pivotal intermediates for the synthesis of 1-β-methyl carbapenem antibioticsTetrahedron, 1996
- Novel Amidoalkylation of 4-Acetoxyazetidinones with Allylic Boranes. A Stereoselective Entry into the TribactamsJournal of the American Chemical Society, 1995
- Stereocontrol by the carbon-fluorine bond and its application to asymmetric synthesis of 3-fluoro .beta.-lactamsThe Journal of Organic Chemistry, 1993
- The ester enolate-imine condensation route to .beta.-lactamsChemical Reviews, 1989
- Silicon-assisted synthesis of β-lactamsTetrahedron, 1988
- Stereospecific synthesis of a chiral intermediate for the preparation of thienamycin, penems, and carbapenems: use of the nitro group as a hydroxy protecting groupJournal of the Chemical Society, Perkin Transactions 1, 1986
- 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
- Preparation by yeast reduction and determination of the sense of chirality of enantiomerically pure ethyl (−)-4,4,4-trichloro-3-hydroxy- and (+)-4,4,4-trifluoro-3-hydroxybutanoateHelvetica Chimica Acta, 1984
- A greatly improved procedure for ruthenium tetroxide catalyzed oxidations of organic compoundsThe Journal of Organic Chemistry, 1981