294847-76-0

Upstream product

• 129145-38-6 (E)-1-(Toluene-4-sulfonyl)-oct-1-en-3-one 
• 129145-42-2 (R)-(+)-(E)-3-acetoxy-1-(p-tolylsulfonyl)-1-octenene 
• 294847-70-4 (R_S,R_C)-(E)-3-acetoxy-1-(p-tolylsulfinyl)-1-octene 

Downstream Products

• 129145-42-2 (R)-(+)-(E)-3-acetoxy-1-(p-tolylsulfonyl)-1-octenene 

Relevant academic research and scientific papers

A new system for catalytic enantioselective reduction of achiral ketones to chiral alcohols. Synthesis of chiral α-hydroxy acids

The reduction of a variety of achiral ketones with catecholborane as stoichiometric reductant and 0.1 equiv of oxazaborolidine 2 as catalyst in toluene at -78°C proceeds in > 95% yield and with enantioselectivities in the range 30:1 to 9:1, depending on s

Efficient preparation of enantiomerically pure (E)-γ-hydroxy-α,β- unsaturated p-tolylsulfoxides using lipase-mediated acylations

(E)-γ-Hydroxy-α,β-unsaturated p-tolylsulfoxides 1 have been efficiently resolved via irreversible enzymatic acylation with lipase PS (Pseudonomas cepacia) and vinyl acetate. (C) 2000 Elsevier Science Ltd.