871518-01-3

Upstream product

• 181139-28-6 (2R,3S,4S)-1,2-cyclohexylidenedioxy-4-methylhex-5-en-3-ol 
• 78008-36-3 (R)-2,3-cyclohexylideneglyceraldehyde 
• 871518-09-1 (2R,3R,4S)-1,2-cyclohexylidenedioxy-4-methylhex-5-en-3-ol 
• 871517-99-6 (2R,4S)-1,2-cyclohexylidenedioxy-4-methylhex-5-en-3-one 
• 871518-00-2 (2R,3R,4S)-3-benzyloxy-1,2-cyclohexylidenedioxy-4-methylhex-5-ene 

Downstream Products

• 871518-10-4 (2R,3R,4S,5S)-3-benzyloxy-1,2-cyclohexylidenedioxy-4,6-dimethylheptyl-5-acetate 
• 871518-03-5 (2R,3R,4S)-3-benzyloxy-1,2-cyclohexylidenedioxy-4,6-dimethylheptan-5-ol 
• 871518-02-4 (2R,3R,4R)-3-benzyloxy-4,5-cyclohexylidenedioxy-2-methylpentanal 

Relevant academic research and scientific papers

An asymmetric synthesis of (-)-prelactone B

An efficient synthesis of (-)-prelactone B has been developed using 1,2-cyclohexylidene glyceraldehyde as the chiral template. The key features of the synthesis were stereoselective crotylation of 1,2-cyclohexylidene glyceraldehyde and enantioselective re