18319-35-2

Usage

InChI:InChI=1S/C15H24O/c1-10-6-7-15-8-12(10)14(3,9-16)13(15)5-4-11(15)2/h6,11-13,16H,4-5,7-9H2,1-3H3

Upstream product

• 118326-10-6 Acetic acid (E)-6-[2-(tert-butyl-dimethyl-silanyloxy)-4,5-dimethoxy-phenyl]-2-methyl-hept-2-enyl ester 
• 118326-09-3 (E)-6-[2-(tert-Butyl-dimethyl-silanyloxy)-4,5-dimethoxy-phenyl]-2-methyl-hept-2-enoic acid methyl ester 
• 118326-15-1 (E)-6-[2-(tert-Butyl-dimethyl-silanyloxy)-4,5-dimethoxy-phenyl]-2-methyl-hept-2-en-1-ol 
• 118326-16-2 tert-Butyl-[4,5-dimethoxy-2-((E)-4-methoxy-1-methyl-but-3-enyl)-phenoxy]-dimethyl-silane 
• 118326-08-2 4-[2-(tert-Butyl-dimethyl-silanyloxy)-4,5-dimethoxy-phenyl]-pentanal 
• 118343-51-4 Acetic acid (3aS,8S,8aS)-5-methoxy-3,8-dimethyl-6,9-dioxo-2,3,6,7,8,8a-hexahydro-1H-3a,7-methano-azulen-8-ylmethyl ester 
• 118326-13-9 Acetic acid (3aS,6S,8S,8aS)-6-hydroxy-5-methoxy-3,6,8-trimethyl-9-oxo-2,3,6,7,8,8a-hexahydro-1H-3a,7-methano-azulen-8-ylmethyl ester 
• 118326-11-7 Acetic acid (3R,3aS,6S,8S,8aS)-6-hydroxy-3,6,8-trimethyl-5,9-dioxo-octahydro-3a,7-methano-azulen-8-ylmethyl ester 
• 118343-53-6 Acetic acid (E)-6-(2-hydroxy-4,5-dimethoxy-phenyl)-2-methyl-hept-2-enyl ester 
• 118326-12-8 C₁₅H₂₀O₃ 
• 100024-95-1 Cedrolsaeuremethylester 
• 18319-39-6 8-Cedren-13-saeure-methylester 

Relevant academic research and scientific papers

Natural products syntheses using anodic oxidation of phenols as a key step

Some bioactive natural products such as terpenoids, neolignans and others have been synthesized by means of an electrochemical method, wherein anodic oxidation of phenols is carried out as a key step.

EFFICIENT SYNTHESIS OF (+/-)-8,14-CEDRANOXIDE USING ELECTROCHEMICAL METHODS AS A KEY STEP

(+/-)-8,14-Cedranoxide has been synthesized starting from 3,4-dimethoxyphenol, wherein 6-acetoxymethyl-2,6-dimethyl-9-methoxytricyclo1,5>undec-9-en-8,11-dione as a key intermediate has been produced efficiently by means of electrochemic