275825-12-2

Upstream product

• 1826-67-1 vinyl magnesium bromide 
• 275825-05-3 (S)-2-methyl-2-(4-methylpent-4-en-1-yl)cyclohexanone 
• 60733-10-0 (S)-seudenol 
• 1344731-00-5 5-(1-methylcyclohex-2-en-1-yl)pent-1-en-3-ol 
• 1344731-15-2 (2S)-2-methyl-2-(4-methylpent-4-en-1-yl)cyclohexanol 
• 1344731-02-7 (2R)-2-methyl-2-(4-methylpent-4-en-1-yl)-7-oxabicyclo[4.1.0]heptanes 
• 1344731-01-6 2-methyl-5-((S)-1-methylcyclohex-2-en-1-yl)pent-1-en-3-yl acetate 

Downstream Products

• 275825-03-1 (S)-6-methyl-6-(4-methylpent-4-en-1-yl)-1-vinylcyclohex-1-ene 

Relevant academic research and scientific papers

Stereoselective alkylation of allylic alcohols: Tandem ethylation and functionalization

A versatile formal SN2 alkylation of allylic alcohols has been devised by means of the Kulinkovich reagent and in situ elaboration of the presumed alkyltitanium intermediates with electrophiles (see scheme). The utility of this method has been