Diastereoselective reductions of β-substituted-γ-keto sulfoximines and a novel palladium(0)-catalysed allylic sulfoximine to allylic sulfinamide rearrangement-Reference-Cited by-同舟云学术

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

Published:1995 Issue:4 Volume: Page:445-446
ISSN:0022-4936
Container-title:J. Chem. Soc., Chem. Commun.
language:en
Short-container-title:J. Chem. Soc., Chem. Commun.

Author:

Pyne Stephen G.,Dong Zemin,Skelton Brian W.,White Allan H.

Publisher

Royal Society of Chemistry (RSC)

Subject

Molecular Medicine

Link

http://pubs.rsc.org/en/content/articlepdf/1995/C3/C39950000445

Reference16 articles.

1. Reduction of β-ketosulfoxides : a highly efficient asymmetric synthesis of both enantiomers of methyl carbinols from the corresponding esters

2. Reduction of β-hydroxysulfoxides: Application to the synthesis of optically active epoxides

3. Highly diastereoselective reduction of chiral β-ketosulphoxides under chelation control: application to the synthesis of (R)-(+)-n-hexadecano-1,5-lactone

4. Studies on the stereoselectivity of hydride reductions on 2-(methylthio)- and 2-(methylsulfonyl)cyclohexanones

5. Highly Diastereoselective Reduction of Ketones in 2-Acyl-2-alkyl-1,3-dithiane 1-Oxides

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