915235-16-4

Upstream product

• 196193-23-4 4-[(1R)-1,5-dimethylhex-4-enyl]cyclohex-2-en-1-one 

Downstream Products

• 915301-61-0 2-methyl-5-((R)-6-methylhept-5-en-2-yl)cyclohex-3-ene-1,2-diol 
• 670260-38-5 (R)-(-)-curcuquinone 
• 69301-25-3 2-methyl-5-[(2R)-6-methylhept-5-en-2-yl]benzene-1,4-diol 
• 915235-15-3 4-hydroxy-2-methyl-4-(2-methylallyl)-5-((R)-6-methylhept-5-en-2-yl)cyclohex-2-enone 
• 915301-63-2 3-methyl-1-(2-methylallyl)-6-((R)-6-methylhept-5-en-2-yl)cyclohex-2-ene-1,4-diol 
• 915235-17-5 2-methyl-5-((R)-6-methylhept-5-en-2-yl)-4-oxocyclohex-2-enyl acetate 
• 915301-62-1 2-hydroxy-2-methyl-5-((R)-6-methylhept-5-en-2-yl)cyclohex-3-enyl acetate 
• 1027144-06-4 5-(1,5-dimethyl-hex-4-enyl)-2-hydroxy-2-methyl-cyclohex-3-enone 
• 30199-27-0 (R)-2-methoxy-1-methyl-4-(6-methylhept-5-en-2-yl)benzene 
• 59684-62-7 (R)-(-)-xanthorrhizol 
• 924888-75-5 6-(3-methoxy-4-methyl-phenyl)-2-methyl-hept-2-enoic acid ethyl ester 
• 1026066-32-9 6-(3-methoxy-4-methyl-phenyl)-2-methyl-hept-2-enoyl chloride 

Relevant academic research and scientific papers

First enantiospecific synthesis of (-)-parvifoline and (-)-curcuquinone

The first enantiospecific synthesis of (-)-parvifoline, employing ring-closing metathesis as the key step, and (-)-curcuquinone from naturally occurring (R)-(+)-citronellal is described.

An enantiospecific synthesis of (+)-isoparvifolinone and (-)-parvifoline

An enantiospecific synthesis of (+)-isoparvifolinone and (-)-parvifoline, from naturally occurring (R)-(+)-citronellal, employing intramolecular Friedel-Crafts acylation as the key step, is described.

The first enantiospecific synthesis of (-)-heritol: absolute configuration determination

The first enantiospecific synthesis of (-)-heritol, from naturally occurring (R)-(+)-citronellal and confirmation of its absolute configuration, is described.