Mild palladium (O)-catalyzed deprotection of allyl esters. A useful application in the synthesis of carbapenems and other β-lactam derivatives.
- 31 December 1987
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 28 (38) , 4371-4372
- https://doi.org/10.1016/s0040-4039(00)96512-2
Abstract
No abstract availableThis publication has 5 references indexed in Scilit:
- Simple and highly diastereoselective synthesis of a 1β-methylcarbapenem key intermediate involving divalent tin enolatesTetrahedron Letters, 1986
- Mild deprotection of carbapenem esters with aluminum trichlorideThe Journal of Organic Chemistry, 1984
- Synthetic Carbapenem Antibiotics. I. 1-b-MethylcarbapenemHETEROCYCLES, 1984
- The Allyl Group as Mildly and Selectively Removable Carboxy‐Protecting Group for the Synthesis of Labile O‐GlycopeptidesAngewandte Chemie International Edition in English, 1984
- Homogeneous, palladium(0)-catalyzed exchange deprotection of allylic esters, carbonates and carbamatesThe Journal of Organic Chemistry, 1982