89461-53-0

Upstream product

• 89461-52-9 (2R,3S)-2,3-epoxyoctanal 
• 2136-75-6 (triphenylphosphoranylidene)acetaldehyde 
• 89461-51-8 [(2S,3S)-3-pentyloxiran-2-yl]methanol 
• 452-51-7 D-2-deoxyribose 
• 89408-79-7 (2R,3S)-1-(tert-Butyl-diphenyl-silanyloxy)-octane-2,3-diol 
• 18409-17-1 (E)-oct-2-en-1-ol 
• 88557-30-6 (2R,3S)-octane-1,2,3-triol 
• 89408-78-6 (Z)-(2R,3S)-1-(tert-Butyl-diphenyl-silanyloxy)-oct-5-ene-2,3-diol 

Downstream Products

• 81918-96-9 14S,15S-epoxy-5Z,8Z,10E,12E-eicosatetraenoic acid 

Relevant academic research and scientific papers

Mammalian blood odorant and chirality: synthesis and sensory evaluation by humans and mice of the racemate and enantiomers of trans-4,5-epoxy-(E)-2-decenal

Abstract The racemate and enantiomers of trans-4,5-epoxy-(E)-2-decenal 1, an odorant with a metallic blood smell, were synthesized. The detection threshold for humans was 0.019 ppb for (2E,4S,5S)-(-)-1 and 0.62 ppb for (2E,4R,5R)-(+)-1, respectively. The

A highly efficient practical method for the synthesis of chiral polyhydroxy-(E,E)-1-chlorodienols and (E)-5-hydroxy enynes

An efficient protocol for the synthesis of chiral polyhydroxy-(E, E)-1-chlorodienols and (E)-5-hydroxy enynes from chiral 4,5-epoxy trans allyl chlorides and 4,5-O-isopropylidene allyl chlorides is described by using stoichiometric amount of LiNH2 or LDA in HMPA : THF (1 : 5) useful in the synthesis of biologically active natural products.

THE STEREOSPECIFIC SYNTHESIS OF 14S,15S-OXIDO 5Z,8Z,10E,12E-EICOSATETRAENOIC ACID

The first total and stereospecific synthesis of 14S,15S-oxido 5Z,8Z,10E,12E-eicosatetraenoic acid from 2-deoxy-D-ribose has been achieved.