One step synthesis of aziridines by the Michael type addition of free sulfimides
- 1 January 1980
- journal article
- Published by Elsevier in Tetrahedron
- Vol. 36 (1) , 73-80
- https://doi.org/10.1016/0040-4020(80)85027-7
Abstract
No abstract availableKeywords
This publication has 42 references indexed in Scilit:
- One Step Synthesis of Optically Active Aziridine with Optically Active o-Methoxyphenyl Phenyl Sulfilimine and OlefinHETEROCYCLES, 1977
- Sulfilimine. I. Synthesis and Formation MechanismBulletin of the Chemical Society of Japan, 1969
- Aziridines. XII. Isolation of a stable nitrogen pyramidJournal of the American Chemical Society, 1968
- Dimethyloxosulfonium Methylide ((CH3)2SOCH2) and Dimethylsulfonium Methylide ((CH3)2SCH2). Formation and Application to Organic SynthesisJournal of the American Chemical Society, 1965
- Studies on Optically Active Amino Acids. V. Synthesis of Optically Active α-Aminoalcohols by the Reduction of α-Amino Acid Esters with Sodium BorohydrideCHEMICAL & PHARMACEUTICAL BULLETIN, 1965
- The Isomerization of Some 1-Aroylaziridines. IIJournal of the American Chemical Society, 1959
- Overlap Control of Carbanionoid Reactions. I. Stereoselectivity in Alkaline EpoxidationJournal of the American Chemical Society, 1959
- A New Method for the Epoxidation of α,β-Unsaturated KetonesJournal of the American Chemical Society, 1958
- The Stereochemistry of Base-catalyzed EpoxidationJournal of the American Chemical Society, 1958
- Stereoisomeric 2,3-Butanediamines, 3-Amino-2-butanols and 2,3-Dimethylethyleneimines; Stereochemistry of the Opening and Closing of the Imine Ring1Journal of the American Chemical Society, 1952