Diastereoselective alkylation of chiral derivatives of acetoacetic acid
- 1 September 1995
- journal article
- Published by Elsevier in Tetrahedron
- Vol. 51 (39) , 10795-10800
- https://doi.org/10.1016/0040-4020(95)00643-m
Abstract
No abstract availableKeywords
This publication has 7 references indexed in Scilit:
- Preparation of transition metal complexes of chiral derivatives of acetoacetic acid. Tetraalkylammonium tetrachlorometallates as an organic source of metalsPolyhedron, 1995
- Camphor derivatives as chiral auxiliaries in asymmetric synthesisTetrahedron, 1987
- Asymmetric synthesis of premonensin, a potential intermediate in the biosynthesis of monensinJournal of the American Chemical Society, 1986
- Asymmetric dialkylation of α-cyanoacetic acidTetrahedron Letters, 1986
- Total synthesis of (+)-pederin. 2. Stereocontrolled synthesis of (+)-benzoylselenopederic acid and total synthesis of (+)-pederinTetrahedron Letters, 1985
- 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 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