153280-70-7

Upstream product

• 153280-68-3 Naphthalen-1-yl-carbamic acid (1S,4R)-4-hydroxy-1-(1-hydroxy-1-methyl-ethyl)-4-methyl-hex-5-enyl ester 
• 153379-78-3 (3R,6S)-6,7-dihydroxy-6,7-dihydrolinalool 
• 126-91-0 linalool 
• 153280-69-4 Naphthalen-1-yl-carbamic acid (1S,4R)-4,5-dihydroxy-1-(1-hydroxy-1-methyl-ethyl)-4-methyl-pentyl ester 

Relevant academic research and scientific papers

Asymmetric dihydroxylation of linalool, nerolidol and citronellyl acetate. Enantioselective synthesis of (3S, 6S)-tetrahydro-2,2,6-trimethyl-6-vinyl-2H-pyran-3-ol

The asymmetric Sharpless' dihydroxylation of linalool, citronellyl acetate and nerolidol was investigated. High diastereo-, enantio- and positional selectivity was observed for the first two terpenes. A highly diastereo- and enantioselective synthesis of (3S,6S)-tetrahydro- 2,2,6-trimethyl-6-vinyl-2H-pyran-3-ol is described.