The palladium(0) catalysed allylation reactions of allylic carbonates with chiral sulfinamide anions to give unstable allylic sulfinamide products are described. These products are readily converted to stable, chiral N-benzoyl or N-tosyl allylic amine derivatives with poor to modest enantiomeric purities (ee 23-41%).
History
Citation
Dong, Z. & Pyne, S. G. (2002). Synthesis of chiral allylic amines via palladium(0) catalysed allylations of allylic carbonates with chiral sulfinamide anions. Sulfur Letters, 25 (1), 37-43.