A mild method for the conversion of proipiolic esters to β-keto esters. application to the formal total synthesis of (±)-thienamycin
- 31 December 1982
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 23 (28) , 2875-2878
- https://doi.org/10.1016/s0040-4039(00)88437-3
Abstract
No abstract availableKeywords
This publication has 6 references indexed in Scilit:
- A practical synthesis of (±)-thienamycinTetrahedron Letters, 1980
- A stereocontrolled synthesis of (+)-thienamycinJournal of the American Chemical Society, 1980
- Thienamycin total synthesis. 1. Synthesis of azetidinone precursors of (.+-.)-thienamycin and its stereoisomersThe Journal of Organic Chemistry, 1980
- Allenic carbanions in synthesis I. The acylacetate unitTetrahedron Letters, 1973
- Cleavage of the carbon‐silicon bond in 1‐alkynylsilanes by silver nitrate: Protection of a terminal triple bond in hydrogenation reactions with the trimethylsilyl groupRecueil des Travaux Chimiques des Pays-Bas, 1967
- Steroids. CII.1 Synthesis of 19-Norprogesterone from Estrone2Journal of the American Chemical Society, 1958