Asymmetric alkylation reactions of camphor-based imide enolate
- 9 September 1991
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 32 (37), 4959-4962
- https://doi.org/10.1016/s0040-4039(00)93507-x
Abstract
No abstract availableThis publication has 26 references indexed in Scilit:
- The enantioselective conversion ofTetrahedron Letters, 1985
- (S)-2-Methoxymethylpyrrolidin - ein chirales AuxiliarNachrichten aus Chemie, Technik und Laboratorium, 1985
- Camphorsulfonamide‐Shielded, Asymmetric 1,4‐Additions and Enolate Alkylations; Synthesis of a Southern Corn Rootworm Pheromone. Preliminary CommunicationHelvetica Chimica Acta, 1985
- Chiral quaternary carbon compounds. II. An asymmetric synthesis of (R) or (S)-4,4-dialkyl-2-cyclopentenonesTetrahedron Letters, 1985
- Enantioselection in the birch reduction-alkylation of a chiral benzoic acid derivativeTetrahedron Letters, 1984
- Asymmetric synthesis of quaternary carbon centersJournal of the American Chemical Society, 1984
- Asymmetric alkylation reactions of chiral imide enolates. A practical approach to the enantioselective synthesis of .alpha.-substituted carboxylic acid derivativesJournal of the American Chemical Society, 1982
- Functional Groups at Concave Sites: Asymmetric Alkylation of Esters with Very High Stereoselectivity and Reversal of Configuration by Change of SolventAngewandte Chemie International Edition in English, 1981
- Asymmetric synthesis of 2-substituted butyrolactones and valerolactonesThe Journal of Organic Chemistry, 1980
- Enantioselective alkylation of chiral enolatesTetrahedron Letters, 1980