Highly -diastereoselective reduction of 2-alkyl-3-oxo amides by potassium triethylborohydride
- 1 January 1985
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 26 (38) , 4643-4646
- https://doi.org/10.1016/s0040-4039(00)98774-4
Abstract
No abstract availableKeywords
This publication has 8 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
- Stereoselectivity in the aldol reactionTetrahedron, 1984
- The stereoselective α-alkylation of chiral β-hydroxy esters and some applications thereofTetrahedron, 1984
- Asymmetric alkylation of carboxyamides by using trans-2,5-disubstituted pyrrolidines as chiral auxiliariesTetrahedron Letters, 1984
- Asymmetric acylation of carboxamides having -2,5-bis(methoxymethoxymethyl)pyrrolidine moiety as a chiral auxiliary and stereoselective reduction of the resulting 2-alkyl-3-oxoamidesTetrahedron Letters, 1984
- Stereoselective reduction of 3-oxo amides with zinc borohydrideTetrahedron Letters, 1983
- Über die Stereospezifität der α‐Alkylierung von β‐Hydroxycarbonsäureestern. Vorläufige MitteilungHelvetica Chimica Acta, 1979
- Torsional strain involving partial bonds. The stereochemistry of the lithium aluminium hydride reduction of some simple open-chain ketonesTetrahedron Letters, 1968