58493-52-0

Upstream product

• 145353-92-0 methyl (1'R,4R)-4-(2'-formyl-1'-methylethyl)cyclohex-1-ene-1-carboxylate 
• 926-62-5 isobutylmagnesium bromide 
• 145353-91-9 methyl (1S,4S,1'S)-(-)-4-(1'-methyl-2'-propenyl)-2-cyclohexenecarboxylate 
• 145414-44-4 methyl (4R,1'S)-(+)-4-(1'-methyl-2'-propenyl)-1-cyclohexencarboxylate 
• 145353-90-8 (1S,4S,1'S)-(-)-4-(1'-methyl-2'-propenyl)-2-cyclohexenylmethanol 
• 145414-43-3 (3aS,7aR)-(+)-2,3,3a,4,5,7a-hexahydrobenzofuran-2-one 
• 145353-87-3 (3S,3aS,7aR)-(+)-methyl-2,3,3a,4,5,7a-hexahydrobenzfuran-2-one 
• 145353-89-5 (1S,6S,1'S)-(+)-2-(1'-methyl-2'-propenyl)-5-cyclohexen-1-ol 
• 68069-67-0 (1S,4S)-(-)-bicyclo<2.2.2>oct-5-en-2-one 
• 145414-45-5 methyl (4R,1'R)-(+)-4-(3'-hydroxypropyl)-1-cyclohexanecarboxylate 
• 162329-04-6 (E,1'S,3R,R_S)-3-(1'-methyl-3'-phenylsulphinyl-2'-propenyl)cyclohexan-1-one 
• 162329-08-0 methyl (E,1'S,4R)-4-(1'-methyl-3'-phenylthio-2'-propenyl)cyclohex-1-ene-1-carboxylate 
• 162329-05-7 (E,1'S,3R)-3-(1'-methyl-3'-phenylthio-2'-propenyl)cyclohexan-1-one 
• 17904-27-7 (+)-(4R)-[(S)-1,5-dimethyl-3-oxohexyl]cyclohex-1-enecarboxylic acid methyl ester 

Downstream Products

• 38963-91-6 4-((R)-1,5-Dimethyl-3-oxo-hexyl)-cyclohexanecarboxylic acid 
• 38963-91-6 4-((R)-1,5-Dimethyl-3-oxo-hexyl)-cyclohexanecarboxylic acid 
• 86279-09-6 cis-4-<3(S)-hydroxy-1(R),5-dimethylhexyl>cyclohexane-1-carboxylic acid 
• 86279-09-6 trans-4-<3(S)-hydroxy-1(R),5-dimethylhexyl>cyclohexane-1-carboxylic acid 
• 38963-60-9 4-((R)-1,5-Dimethyl-3-oxo-hexyl)-cyclohexanecarboxylic acid methyl ester 
• 17844-06-3 (R)-4-((R)-3-Hydroxy-1,5-dimethyl-hexyl)-cyclohex-1-enecarboxylic acid 
• 17904-27-7 (+)-(4R)-[(S)-1,5-dimethyl-3-oxohexyl]cyclohex-1-enecarboxylic acid methyl ester 
• 6753-22-6 (+/-)-Epitodomatusaeure 
• 16981-74-1 (+/-)-erythro-juvabione 

Relevant academic research and scientific papers

Synthesis of compounds with juvenile hormone activity; XXXI: Stereocontrolled synthesis of (+)-juvabione from a chiral sulfoxide

A stereocontrolled synthesis of (+)-juvabione is described. The key step is a regioselective lithiation of a chiral (E)-butenyl sulfoxide 5 followed by stereoselective 1,4-addition to cyclohex-2-en-1-one. The chiral sulfoxide 5 was prepared by employing a

Synthesis of (+)-Juvabione, a Compound with Juvenile Hormone Activity

(+)-Juvabione 1 was synthesized by employing (1R,4S,6S)-6-hydroxybicyclooctan-2-one 2 as a chiral source. (+)-Juvabione 1 shows juvenile hormone activity, and its racemate has been repeatedly synthesized.Optically active 1 was synthesized by Pawson