129150-03-4

Upstream product

• 129150-18-1 (E)-7-(4-methoxyphenyl)-4-methylhept-4-en-1-ol 
• 129150-17-0 (E)-7-(4-Methoxy-phenyl)-4-methyl-hept-4-enoic acid ethyl ester 
• 122410-19-9 5-(4-Methoxyphenyl)-2-methylpent-1-en-3-ol 
• 20401-88-1 3-(4-methoxyphenyl)propional 

Downstream Products

• 1402736-05-3 (E)-2-(6-(4-methoxyphenyl)-3-methylhex-3-en-1-yl)-1,3-dioxane 
• 129150-04-5 (E)-1-<8,8-(1,2-Benzenediyldithio)-4-methylocta-3,7-dienyl>-4-methoxybenzene 

Relevant academic research and scientific papers

Asymmetric syntheses of 8-oxabicyclo[3,2,1]octanes: A cationic cascade cyclization

High octane: A novel and practical syntheses of 8-oxabicyclo[3.2.1]octanes using a cationic cascade cyclization reaction has been developed (see scheme; TIPS=triisopropylsilyl). The diastereomer of the cyclization product isolated depends upon whether the acetal or aldehyde substrate is used. Copyright

1,3-Benzodithiolium Cation Mediated Cyclization Reactions

General protocols for the construction of various ring systems employing cation olefin cyclizations initiated by the readily accessible 1,3-benzodithiolium ion are described.Several substituted tetralones and tetralins can be rapidly assembled by this methodology as can a variety of substituted bicyclooctane and tricyclic ring systems.The products of these transformations are amenable to interconversion into a range of functionalized species.