82538-58-7

Upstream product

• 82538-56-5 (S)-(+)-3-methylpentane-1,5-diol 1-benzyl ether 
• 161905-08-4 (S,E)-8-(benzyloxy)-2,6-dimethyl-3-octen-2-ol 
• 61898-56-4 (S)-4-methyltetrahydro-2H-pyran-2-one 
• 100-44-7 benzyl chloride 
• 220272-09-3 ((S)-3-Methyl-hex-5-enyloxymethyl)-benzene 
• 87144-80-7 methyl (R)-(+)-7-hydroxy-3,7-dimethyl-5-octenoate 
• 82538-57-6 [(R)-5-(2-Methoxy-ethoxymethoxy)-3-methyl-pentyloxymethyl]-benzene 
• 135559-20-5 (R)-3,7-dimethyl-5-octene-1,7-diol 
• 82538-55-4 (R)-3-methylpentane-1,5-diol 1-MEM ether 
• 72604-84-3 (S)-5-(2-Methoxy-ethoxymethoxy)-3-methyl-pentanal 
• 20425-48-3 methyl (R)-(+)-citronellate 

Downstream Products

• 82538-59-8 (3RS,5R)-(-)-7-benzyloxy-2-isopropyl-5-methyl-1-hepten-3-ol 
• 1207192-63-9 (2S,4R,6S)-2-((R)-4-(benzyloxy)-2-methylbutyl)-6-(hydroxymethyl)-tetrahydro-2H-pyran-4-ol 

Relevant academic research and scientific papers

Cyclopropanol Methodology in the Synthesis of (4R)- and (4S)-4-Methyltetrahydro-2H-pyran-2-ones. Application in the Synthesis of Insect Pheromones with Methyl-Branched Carbon Skeleton

A number of chiral methyl-branched building blocks have been synthesized starting from (4S)-4-methyltetrahydro-2H-pyran-2-one, and the possibility for using them for the preparation of mealworm beetle, rhinoceros beetle, and earth-boring dung beetle phero

Enantiospecific formal total synthesis of iriomoteolide 3a

A formal total synthesis of the marine macrolide iriomoteolide 3a is described. Salient features of the synthesis include the elaboration of a β-keto phosphonate derived from d-(-)-tartaric acid and the extension of a chiral butyrolactone derived from L-g

A concise stereoselective formal total synthesis of the cytotoxic macrolide (+)-Neopeltolide via Prins cyclization

A convergent and highly stereoselective formal total synthesis of the naturally occurring, cytotoxic 14-membered macrolide neopeltolide has been achieved via two Prins cyclizations.