79082-41-0

Upstream product

• 110-87-2 3,4-dihydro-2H-pyran 
• 79120-18-6 (3S)-3-<<(2R,S)-3,4,5,6-Tetrahydro-2H-pyran-2-yl>oxy>-1-butanol 
• 98-59-9 p-toluenesulfonyl chloride 
• 79016-08-3 (3S)-3-<<(2R,S)-3,4,5,6-Tetrahydro-2H-pyran-2-yl>oxy>buttersaeure-ethylester 

Downstream Products

• 120876-13-3 (S)-(+)-1-methyldodecyl acetate 
• 85852-46-6 (R)-4-tetrahydropyranyloxy-1-pentyl tosylate 
• 85852-46-6 (S)-4-tetrahydropyranyloxy-1-pentyl tosylate 

Relevant academic research and scientific papers

Insect pheromones and their analogs. LX. Stereocontrolled synthesis of sex pheromones of Drosophila mulleri and Mayetiola destructor

Syntheses are developed for 2S-tridecyl-and 2S-tridec-10E-enylacetates, sex pheromones of the fruit fly Drosophila mulleri and the Hessian fly Mayetiola destructor, respectively, that are based on ethyl-3S-hydroxybutanoate, a product from enzymatic reduction of ethyl acetoacetate by the soil yeast strain "80-1.".

A SIMPLE SYNTHESIS OF (S)-(+)-SULCATOL, THE PHEROMONE OF GNATHOTRICHUS RETUSUS, EMPLOYING BAKER'S YEAST FOR ASYMMETRIC REDUCTION

Ethyl (S)-3-hydroxybutanoate of 87percent optical purity was obtained by the yeast reduction of ethyl acetoacetate and was converted into 85-87percent optically pure (S)-(+)-sulcatol (6-methyl-5-hepten-2-ol) by a 5-step sequence in 73percent overall yield.