175230-84-9

Upstream product

• 6007-23-4 2-ethyl-1,3-dithiane 
• 104-53-0 3-phenyl-propionaldehyde 

Downstream Products

• 175230-85-0 2-(3-phenylpropanoyl)-2-ethyl-1,3-dithiane 
• 332048-55-2 (+)-2-(2-(N,N'-bis(t-butoxycarbonyl)hydrazino)-3-phenylpropanoyl)-2-(R)-ethyl-1,3-dithiane 1-(R)-oxide 
• 332049-80-6 (+/-)-2-(2-(N,N'-bis(t-butoxycarbonyl)hydrazino)-3-phenylpropanoyl)-2-ethyl-1,3-dithiane 
• 332048-60-9 (-)-2-(S)-(N,N'-bis(t-butoxycarbonyl)hydrazino)-1-phenylhexan-3,4-dione 
• 175417-34-2 (+)-2-(R)-(3-phenylpropanoyl)-2-ethyl-1,3-dithiane 1-(R)-oxide 

Relevant academic research and scientific papers

Enantioselective preparation of 2-substituted-1,3-dithiane 1-oxides using modified Sharpless sulphoxidation procedures

Enantioselective sulphoxidation of a wide range of 2-substituted-1,3-diathianes has been carried out using modified Sharpless conditions to furnish the corresponding sulphoxides in optically enriched form. Deacylation of 2-acyl-1,3-dithiane 1-oxide deriva

Electrophilic amination of ketone enolates mediated by the DiTOX asymmetric building block: Enantioselective formal synthesis of α-aminoacids

Diastereoselective electrophilic amination of enolates derived from 2-acyl-1,3-dithiane 1-oxides is used as the key step for an enantioselective synthesis of two α-hydrazido carboxylic acids, well-known precursors of α-amino acids. (C) 2000 Elsevier Science Ltd.