80527-39-5

Upstream product

• 80527-38-4 Acetic acid 1,1-dimethyl-5-methylene-2-phenylsulfanyl-hept-6-enyl ester 
• 931-59-9 benzenesulfenyl chloride 
• 70473-42-6 [1-(1-Chloro-1-methyl-ethyl)-4-methylene-hex-5-enylsulfanyl]-benzene 
• 123-35-3 7-methyl-3-methene-1,6-octadiene 

Downstream Products

• 14434-41-4 ipsdienol 

Relevant academic research and scientific papers

Facile Regio- and Stereo-specific Allylic Oxidation of gem-Dimethyl Olefins via Addition of Benzenesulphenyl Chloride. Synthesis of Allylic Oxygenated Terpenes

Novel and facile terminal trans-allylic and internal allylic oxidations of the gem-dimethyl olefin terminus of the terpenoids (1) are described which take place site-, regio-, and stereo-specificially via the same intermediate adduct between benzenesulphenyl chloride and (1).By this method, the allylic oxygenated terpenes (+/-)-nuciferal (11), (+/-)-ar-turmerone (12), (+/-)-ipsdienol (3c), neotorreyol (2e), (+/-)-6-hydroxydendrolasin (3e), and 6-oxodendrolasin (14) were synthesized.