The synthesis of amino acids by 1,3-dipolar cycloadditions of azomethine ylides
- 1 January 1985
- journal article
- research article
- Published by Elsevier in Tetrahedron
- Vol. 41 (17) , 3537-3545
- https://doi.org/10.1016/s0040-4020(01)96707-9
Abstract
No abstract availableThis publication has 34 references indexed in Scilit:
- The Isoxazoline Route to α-Methylen Lactones.Tetrahedron Letters, 2001
- Stereospecific synthesis of racemic daunosamine. Diastereofacial selectivity in a nitrone cycloadditionJournal of the American Chemical Society, 1983
- The direct generation of N-acyl formimidate methylides. An efficient approach to the synthesis of pyrrolidine derivativesJournal of the Chemical Society, Chemical Communications, 1983
- Reduction of Δ2-isoxazolines-2. A facile synthesis of 3(2H)-furanones.Tetrahedron Letters, 1983
- A stereoselective synthesis of α-isosparteineJournal of the Chemical Society, Chemical Communications, 1983
- Stereospecific synthesis of retronecine by imidate methylide cycloadditionJournal of the American Chemical Society, 1980
- Methylides from trimethylsilylmethylsulfonium, -ammonium, -immonium, and -phosphonium saltsJournal of the American Chemical Society, 1979
- Mechanism of 1,3-dipolar cycloadditions. ReplyThe Journal of Organic Chemistry, 1968
- Mechanism of 1,3-dipolar cycloadditionsThe Journal of Organic Chemistry, 1968
- The Formation of Pyrrocolines by the Reaction of Dimethyl Acetylenedicarboxylate with Heterocyclic Zwitterions1Journal of the American Chemical Society, 1961