Diastereoselective reductions of ß-substituted-¿-keto sulfoximines and a novel palladium(0)-catalysed allylic sulfoximine to allylic sulfinamide rearrangement

Citation

• Pyne, S. G., Dong, Z., Skelton, B. W., & White, A. H. (1995). Diastereoselective reductions of ß-substituted-¿-keto sulfoximines and a novel palladium(0)-catalysed allylic sulfoximine to allylic sulfinamide rearrangement. Journal of the Chemical Society, Chemical Communications, (4), 445-446. doi:10.1039/C39950000445

Digital Object Identifier (doi)

• 10.1039/C39950000445

Scopus Eid

• 2-s2.0-0028920762

Web Of Science Accession Number

Start Page

• 445

End Page

• 446

Issue

• 4

Abstract

• The reduction of β-substituted-γ-keto N-tosyl sulfoximines is highly diastereoselective and the allylic sulfoximines products undergo a facile rearrangement to allylic sulfinamides in the presence of a palladium(0) catalyst.

UOW Authors

•   Pyne, Stephen

Publication Date

• 1995

Publisher

• Royal Society of Chemistry (RSC) 

Published In

• Journal of the Chemical Society, Chemical Communications  Journal

Citation

• Pyne, S. G., Dong, Z., Skelton, B. W., & White, A. H. (1995). Diastereoselective reductions of ß-substituted-¿-keto sulfoximines and a novel palladium(0)-catalysed allylic sulfoximine to allylic sulfinamide rearrangement. Journal of the Chemical Society, Chemical Communications, (4), 445-446. doi:10.1039/C39950000445

Digital Object Identifier (doi)

• 10.1039/C39950000445

Scopus Eid

• 2-s2.0-0028920762

Web Of Science Accession Number

Start Page

• 445

End Page

• 446

Issue

• 4