87106-23-8

Upstream product

• 87106-22-7 (R,E)-(+)-7-hydroxy-3,7-dimethyl-5-octenyl benzyl ether 
• 112604-91-8 (S)-3-methyl-5-(t-butyldimethylsilyloxy)-1-pentanol 
• 1046471-51-5 (R)-propyl 5-hydroxy-3-methylpentanoate 
• 83541-12-2 (R)-(+)-citronellyl benzyl ether 

Downstream Products

• 87106-34-1 (3R,7S)-3,7-dimethylnonyl tosylate 
• 87106-30-7 (3R,7R)-3,7-dimethylnonyl tosylate 
• 87106-32-9 (3R,7S)-(+)-dimethylnonyl benzyl ether 
• 639859-79-3 ((3R,7R)-3,7-Dimethyl-nonyloxymethyl)-benzene 
• 87106-28-3 (3R,7R)-3,7-dimethyl-6-benzenesulfonylnonyl benzyl ether 
• 87118-41-0 (S)-1-(benzyloxy)-5-iodo-3-methylpentane 
• 87106-24-9 (S)-3-methyl-1,5-pentanediol monotosylate monobenzyl ether 

Relevant academic research and scientific papers

Stereoselective synthesis of the C3-C15 fragment of callyspongiolide

The synthesis of C3-C15 fragment of callyspongiolide, a 14-membered macrolides isolated from the marine sponge Callyspongia sp., which was collected from the Indonesia, is reported. Highlights of the synthesis include construction of E-olefin through Juli

SYNTHESIS OF ALL OF THE FOUR POSSIBLE STEREOISOMERS OF 4,8-DIMETHYLDECANAL, THE AGGREGATION PHEROMONE OF THE FLOUR BEETLES

The four stereoisomers of 4,8-dimethyldecanal were synthesized employing organometallic or electrolytic coupling reactions as the key step.The response of the red flour beetle, Tribolium castaneum, to the (4R,8R)-isomer was identical with that to the natural pheromone, while other isomers induced only very weak or no responses.The (4R,8R)-isomer is therefore the natural pheromone.