Asymmetric acylation of carboxamides having -2,5-bis(methoxymethoxymethyl)pyrrolidine moiety as a chiral auxiliary and stereoselective reduction of the resulting 2-alkyl-3-oxoamides
- 1 January 1984
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 25 (52) , 6015-6016
- https://doi.org/10.1016/s0040-4039(01)81747-0
Abstract
No abstract availableKeywords
This publication has 4 references indexed in Scilit:
- Asymmetric acylation reactions of chiral imide enolates. The first direct approach to the construction of chiral .beta.-dicarbonyl synthonsJournal of the American Chemical Society, 1984
- Asymmetric alkylation of carboxyamides by using trans-2,5-disubstituted pyrrolidines as chiral auxiliariesTetrahedron Letters, 1984
- Stereoselective reduction of 3-oxo amides with zinc borohydrideTetrahedron Letters, 1983
- Stereoselective reduction of β-keto esters with zinc borohydride. stereoselective synthesis of -3-hydroxy-2-alkylpropionatesTetrahedron Letters, 1980