943154-99-2

Upstream product

• 362505-14-4 (2R)-1,2-(cyclohexylidenedioxy)hex-5-en-3-one 
• 362505-12-2 (2R,3S/R)-1,2-(cyclohexylidenedioxy)hex-5-en-3-ol 
• 943154-97-0 (2R,3S)-1-(benzoyloxy)-3-(benzyloxy)-3-methylhex-5-ene-2-ol 
• 943154-96-9 (2R,3S)-3-(benzyloxy)-3-methylhex-5-ene-1,2-diol 
• 943154-95-8 (2R,3S)-3-(benzyloxy)-1,2-(cyclohexylidenedioxy)-3-methylhex-5-ene 
• 943154-93-6 (2R,3S)-1,2-(cyclohexylidenedioxy)-3-methylhex-5-en-3-ol 
• 943154-98-1 C₂₂H₂₆O₆S 

Downstream Products

• 145263-42-9 (R)-3-(benzyloxy)-3-methy-5-hexanolide 

Relevant academic research and scientific papers

An efficient asymmetric route to tertiary carbinols: Synthesis of (R)-mevalonolactone

An efficient strategy for the asymmetric construction of tertiary carbinols has been devised using cyclohexylideneglyceraldehyde as a chiral template. This involves (a) addition of a Grignard reagent (R1MgX) to cyclohexylideneglyceraldehyde, fo