59664-63-0

Upstream product

• 72623-61-1 (2E,6E,10Z)-14-Isopropenyl-3,7,11-trimethyl-cyclotetradeca-2,6,10-trienone 
• 58220-80-7 (2E,6E,10Z)-(S)-14-Isopropenyl-3,7,11-trimethyl-cyclotetradeca-2,6,10-trienone 
• 59664-63-0 (2E,6E,10Z)-(1R,14S)-14-Isopropenyl-3,7,11-trimethyl-cyclotetradeca-2,6,10-trienol 

Downstream Products

• 59664-63-0 (2E,6E,10Z)-(1S,14S)-14-Isopropenyl-3,7,11-trimethyl-cyclotetradeca-2,6,10-trienol 
• 107099-14-9 Benzoic acid (E)-(2R,5S,7S,12S,13R)-2-bromo-13-isopropenyl-1,5-dimethyl-6,16-dioxa-tricyclo[10.3.1.0^5,7]hexadec-10-en-10-ylmethyl ester 
• 107099-14-9 Benzoic acid (E)-(2S,5S,7S,12R,13S)-2-bromo-13-isopropenyl-1,5-dimethyl-6,16-dioxa-tricyclo[10.3.1.0^5,7]hexadec-10-en-10-ylmethyl ester 
• 64180-67-2 (+/-)-asperdiol 
• 86838-72-4 rel-(1R,2S)-(3E,7E,11E)-1-isopropenyl-4-<(benzoyloxy)methyl>-8,12-dimethyl-3,7,11-cyclotetradecatrien-2-ol 
• 107099-13-8 Benzoic acid (2E,6E)-(1S,10R,14R)-10-bromo-14-isopropenyl-7,11-dimethyl-15-oxa-bicyclo[9.3.1]pentadeca-2,6-dien-3-ylmethyl ester 
• 107099-14-9 Benzoic acid (E)-(1R,2R,5S,7S,12R,13S)-2-bromo-13-isopropenyl-1,5-dimethyl-6,16-dioxa-tricyclo[10.3.1.0^5,7]hexadec-10-en-10-ylmethyl ester 
• 107171-98-2 Benzoic acid (E)-(1S,2S,5S,7S,12S,13R)-2-bromo-13-isopropenyl-1,5-dimethyl-6,16-dioxa-tricyclo[10.3.1.0^5,7]hexadec-10-en-10-ylmethyl ester 
• 86838-72-4 Benzoic acid (1Z,7E,11E)-(3R,4S)-3-hydroxy-4-isopropenyl-7,11-dimethyl-cyclotetradeca-1,7,11-trienylmethyl ester 
• 107171-97-1 Benzoic acid (1Z,7E,11E)-(3R,4R)-3-hydroxy-4-isopropenyl-7,11-dimethyl-cyclotetradeca-1,7,11-trienylmethyl ester 
• 107114-68-1 C₃₄H₄₀O₅ 
• 107099-15-0 C₃₄H₄₀O₄ 
• 107099-13-8 Benzoic acid (2E,6E)-(1R,10R,11R,14S)-10-bromo-14-isopropenyl-7,11-dimethyl-15-oxa-bicyclo[9.3.1]pentadeca-2,6-dien-3-ylmethyl ester 
• 39012-00-5 (+/-)-mukulol 

Relevant academic research and scientific papers

PREPARATION OF ENANTIOMERICALLY PURE 1-HYDROXY-NEOCEMBRENES TO DETERMINE THE UNSOLVED ABSOLUTE CONFIGURATION OF CEMBRENOIDS

Cis and trans 1-hydroxy-neocembrenes were prepared in an enantiomerically pure form by reduction of dl-ketone with respective (+)- and (-)-Darvon-LiAlH4 complex followed by purification with the aids of esterification with d- and l-menthoxyacetyl chlorides and (-)-camphanic acid chloride, respectively.Absolute configuration of naturally occurring (+)-mayol and (+)-cembrenene was determined by correlation with enantiomerically pure compounds.