308795-22-4

Upstream product

• 78008-36-3 (S)-cyclohexylidene glyceraldehyde 
• 229639-21-8 3,4-O-cyclohexylidene-L-(S)-erythrulose 
• 229639-27-4 (S)-1-(1,4-Dioxa-spiro[4.5]dec-2-yl)-ethane-1,2-diol 
• 100-52-7 benzaldehyde 
• 308795-19-9 (2S)-1,2-O-cyclohexylidene-1,2-dihydroxypentan-3-one 

Relevant academic research and scientific papers

Stereoselective synthesis of syn-α-methyl-β-hydroxy esters

Boron enolates of an ethyl ketone structurally related to erythrulose react with achiral aldehydes in a highly stereoselective fashion to yield 1,2-syn/1,3-syn stereoisomers. Oxidative cleavage of the aldol adducts yields enantiopure O-formylated syn-α-me