CHIRALITY INVERSION OF THE 1,3-GLYCOL SYSTEM AND ITS APPLICATION TO THE SYNTHESIS OF THE CARBAPENEM INTERMEDIATE
- 5 February 1983
- journal article
- Published by Oxford University Press (OUP) in Chemistry Letters
- Vol. 12 (2) , 175-176
- https://doi.org/10.1246/cl.1983.175
Abstract
No abstract availableThis publication has 9 references indexed in Scilit:
- Regioselective reductions of 2,3-epoxy alcoholsTetrahedron Letters, 1982
- Synthesis of saccharides and related polyhydroxylated natural products. 1. Simple alditolsThe Journal of Organic Chemistry, 1982
- Reductive ring openings of allyl-alcohol epoxidesTetrahedron Letters, 1982
- Ph3P-(PyS)2-CH3CN as an excellent condensing system for .beta.-lactam formation from .beta.-amino acidsJournal of the American Chemical Society, 1981
- Chirale elektrophile Synthesebausteine mit vier verschiedenen funktionellen Gruppen aus Weinsäure, 2, 3‐ und 3, 4‐Epoxy‐butandiolderivate in allen vier stereoisomeren FormenHelvetica Chimica Acta, 1981
- A mercury mediated route to the mitosenesTetrahedron Letters, 1981
- A stereocontrolled synthesis of (+)-thienamycinJournal of the American Chemical Society, 1980
- Stereospecific and stereoselective reactions. I. Preparation of amines from alcoholsJournal of the American Chemical Society, 1972
- The Chemical Reaction in Silent Electric Discharge. IBulletin of the Chemical Society of Japan, 1961