Asymmetric synthesis via nucleophilic addition to α,β-epoxyimines
- 2 June 1992
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 33 (23) , 3355-3358
- https://doi.org/10.1016/s0040-4039(00)92087-2
Abstract
No abstract availableThis publication has 18 references indexed in Scilit:
- A stereochemically general synthesis of 2-deoxyhexoses via the asymmetric allylboration of 2,3-epoxy aldehydesThe Journal of Organic Chemistry, 1991
- Stereoselective synthesis of 3-(ethoxycarbonyl)-4-hydroxy-5-(1-hydroxyalkyl)-2-isoxazoline 2-oxides by reaction of 2,3-epoxy aldehydes and ethyl nitroacetate on alumina surfaceThe Journal of Organic Chemistry, 1990
- The asymmetric synthesis of β-lactam antibiotics-v. Application of chiral α,β-epoxyimines in ketene-imine cycloaddition reactions leading to homochiral 3-aminoazetidinones.Tetrahedron Letters, 1988
- Stereoselective additions to α,β-epoxy-aldehydes; the formation of “non-chelation controlled” productsTetrahedron Letters, 1987
- Facile preparation of (2R,3S)- and (2S,3R)-3-[[(4-bromobenzyl)oxy]methyl]oxirane-2-methanol via asymmetric epoxidationThe Journal of Organic Chemistry, 1987
- High diastereoselectivity observed in the vinylation reaction of α,β-epoxy aldehydes with β-silylphosphorous ylideTetrahedron Letters, 1987
- Calcium in liquid ammonia for the reduction of benzyl ethers. Mechanistic clues derived from chemoselectivity studiesThe Journal of Organic Chemistry, 1986
- Very high 1,2- and 1,3-asymmetric induction in the reactions of allylic boron compounds with chiral iminesJournal of the American Chemical Society, 1986
- Stereocontrolled synthesis of 1,3,5…(2n+ 1) polyolsJournal of the Chemical Society, Chemical Communications, 1982
- Asymmetric epoxidation provides shortest routes to four chiral epoxy alcohols which are key intermediates in syntheses of methymycin, erythromycin, leukotriene C-1, and disparlureJournal of the American Chemical Society, 1981