Asymmetric conjugate addition reaction by the use of ()-γ-trityloxymethyl-γ-butyrolactam as a chiral auxiliary
- 1 January 1986
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 27 (3) , 369-372
- https://doi.org/10.1016/s0040-4039(00)84021-6
Abstract
No abstract availableThis publication has 12 references indexed in Scilit:
- Control elements in the asymmetric tandem alkylation of α-alkylidene-γ-butyrolactone derivativesTetrahedron Letters, 1985
- ENANTIOSELECTIVE CONJUGATE ADDITION REACTION MEDIATED BY CHIRAL LIGANDSChemistry Letters, 1985
- Camphorsulfonamide‐Shielded, Asymmetric 1,4‐Additions and Enolate Alkylations; Synthesis of a Southern Corn Rootworm Pheromone. Preliminary CommunicationHelvetica Chimica Acta, 1985
- Asymmetric synthesis of β-substituted δ-ketoesters via michael-additions of samp/ramp-hydrazones to α,β-unsaturated esters, virtually complete 1.6-asymmetric inductionTetrahedron Letters, 1983
- Enantioselective aldol condensations. 2. Erythro-selective chiral aldol condensations via boron enolatesJournal of the American Chemical Society, 1981
- Syntheses of (S)-5-substituted 4-aminopentanoic acids: a new class of .gamma.-aminobutyric acid transaminase inactivatorsThe Journal of Organic Chemistry, 1980
- Chelation-controlled nucleophilic additions. 1. A highly effective system for asymmetric induction in the reaction of organometallics with α-alkoxyketones.Tetrahedron Letters, 1980
- Stereochemistry in trivalent nitrogen compounds. XXVIII. Conformational analysis and torsional barriers of imides and triamidesJournal of the American Chemical Society, 1975
- Conformational analysis by lanthanide induced shifts. I. Applications to .alpha.,.beta.-unsaturated aldehydes, ketones, esters, and amidesJournal of the American Chemical Society, 1973
- The Dipole Moment and Structure of the Imide Group. II. Semicyclic Imides: N-Acetyl Lactams, Effect of Ring Size on Dipole Moment; N-Benzoyl Lactams, Ring Size, Dipole Moment and Ultraviolet SpectraJournal of the American Chemical Society, 1962