Synthesis of pyrrolidines using an α-cyanoaminosilane as an azomethine ylide equivalent
- 1 January 1983
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 24 (33), 3447-3450
- https://doi.org/10.1016/s0040-4039(00)86009-8
Abstract
No abstract availableThis publication has 14 references indexed in Scilit:
- A new trimethylsilyl triflate-catalyzed 1,3-dipolar cycloaddition leading to pyrrolidinesTetrahedron Letters, 1982
- 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
- Electrophilic Substitution of Organosilicon Compounds- Applications to Organic SynthesisSynthesis, 1979
- Silicon in organic synthesisChemical Society Reviews, 1978
- The molecules R2CXCR2 including azomethine, carbonyl and thiocarbonyl ylides. Their syntheses, properties and reactionsTetrahedron, 1976
- 1,3-Dipolar cycloaddition reactions of the geometrical isomers of some methyl 1-alkyl-2-(p-biphenylyl)-3-aziridinecarboxylatesThe Journal of Organic Chemistry, 1970
- Stereospecific Conversion of cis-trans Isomeric Aziridines to Open-Chain Azomethine YlidesJournal of the American Chemical Society, 1967
- Reactions of aziridines with dimethylacetylene dicarboxylateTetrahedron Letters, 1965
- Aziridines XI. Reaction of 1,2,3-triphenylaziridine with diethylacetylene dicarboxylate and maleic anhydrideTetrahedron Letters, 1965