Asymmetric aziridination by reaction of chiral N-sulfinylimines with sulfur ylides: Stereoselectivity improvement by use of tert-butylsulfinyl group as chiral auxiliary
- 31 December 1996
- journal article
- Published by Elsevier in Tetrahedron: Asymmetry
- Vol. 7 (12) , 3407-3414
- https://doi.org/10.1016/s0957-4166(96)00448-x
Abstract
No abstract availableKeywords
This publication has 8 references indexed in Scilit:
- Addition of dimethyloxosulfonium methylide to enantiomerically pure sulfinimines: Asymmetric synthesis of 2-substituted aziridinesTetrahedron: Asymmetry, 1995
- On the reaction of chiral sulfinimines with sulfur ylides: a novel route to the asymmetric aziridinationTetrahedron Letters, 1995
- Asymmetric synthesis of optically pure tert-butyl sulfoxides using the “DAG methodology”Tetrahedron Letters, 1994
- Chiral Aziridines—Their Synthesis and Use in Stereoselective TransformationsAngewandte Chemie International Edition in English, 1994
- A convenient synthesis of 2-methoxy-1-naphthyl sulfoxides in high enantiomeric purity. A new asymmetric synthesis of 1-benzyl-1,2,3,4-tetrahydroisoquinolinesTetrahedron Letters, 1994
- Asymmetric synthesis of sulfinimines: Chiral ammonia imine synthonsTetrahedron Letters, 1993
- Stereocontrolled synthesis via chiral aziridinesPure and Applied Chemistry, 1993
- Chemistry of sulfoxides and related compounds. XLVIII. Mechanism of nucleophilic alkylidene transfer by sulfonium and oxosulfonium ylidesJournal of the American Chemical Society, 1973