935476-11-2

Upstream product

• 935476-09-8 (6R)-2-methyl-6-((1S,4S)-4-triethylsiloxycyclohex-2-enyl)heptan-4-ol 
• 935476-06-5 (3R)-((1S,4S)-4-triethylsiloxycyclohex-2-enyl)butyraldehyde 
• 935476-05-4 (1R,4R,5R,8S)-8-triethylsiloxy-4-methylbicyclo[3.3.1]nonan-2-one 
• 935476-04-3 (1R,4R,5R,8S)-8-hydroxy-4-methylbicyclo[3.3.1]nonan-2-one 
• 935476-03-2 (1R,4R,5R,8S)-8-methoxymethoxy-4-methylbicyclo[3.3.1]nonan-2-one 
• 935476-10-1 (4S)-4-((1R)-3-benzyloxymethoxy-1,5-dimethylhexyl)cyclohex-2-enone 
• 935476-13-4 (1S,4S)-4-((1R)-3-benzyloxymethoxy-1,5-dimethylhexyl)cyclohex-2-enol 
• 866398-00-7 (1R,5R,8S)-8-methoxymethoxybicyclo[3.3.1]non-3-en-2-one 

Downstream Products

• 42719-55-1 (4R)-4-((1R)-1,5-dimethyl-3-oxohexyl)cyclohex-1-enecarbaldehyde 
• 17904-27-7 (+)-(4R)-[(S)-1,5-dimethyl-3-oxohexyl]cyclohex-1-enecarboxylic acid methyl ester 

Relevant academic research and scientific papers

Enantio- and diastereocontrolled synthesis of (+)-juvabione employing organocatalytic desymmetrisation and photoinduced fragmentation

(+)-Juvabione, a natural sesquiterpene exhibiting insect juvenile hormone activity, has been synthesized from σ-symmetric 4-(2-formylethyl) cyclohexanone by employing organocatalytic asymmetric aldolisation and Norrish I-type fragmentation as the key step