113393-92-3

Upstream product

• 24183-02-6 (E)-<8-(1,3-dioxolan-2-yl)-4-methyl>non-4-en-1-al 
• 24067-42-3 E,E-dimethyl-4,8 ethylenedioxy-12,12 tridecadiene-4,8 al 
• 113393-86-5 E,E,E-dimethyl-6,10 ethylenedioxy-14,14 pentadecatriene-2,6,10 oate d'ethyle 
• 113393-87-6 E,E,E-dimethyl-6,10 ethylenedioxy-14,14 pentadecatriene-2,6,10 ol-1 
• 113393-89-8 E,E,E-chloro-1 dimethyl-6,10 ethylenedioxy-14,14 pentadecatriene-2,6,10 
• 143733-88-4 2-Methyl-2-(2-propenyl)-1,3-dioxolane 
• 24099-78-3 E-dimethyl-2,6 ethylenedioxy-10,10 vinyloxy-3 undecadiene-1,6 
• 24035-32-3 E-ethylenedioxy-10,10 dimethyl-2,6 hydroxy-3 undecadiene-1,6 
• 24108-31-4 6,6-ethylenedioxy-2-methyl-3-vinyloxy-1-heptene 
• 24108-30-3 Ethylene Ketal of 5-Hydroxy-6-methyl-6-hexen-2-one 
• 113393-90-1 E,E,E-para-toluenesulfonyl-1 dimethyl-6,10 ethylenedioxy-14,14 pentadecatriene-2,6,10 

Downstream Products

• 113393-93-4 E,E,E-hydroxy-4-para-toluenesulfonyl-3 trimethyl-4,8,12 cycloctetradecatriene-1,7,11 (cembrene) 

Relevant academic research and scientific papers

Syntheses stereoselectives d'E,E,E-pentadecatrienes-2,6,10 fonctionnalises en position 1 et 14

The synthesis is described of various 6,10-dimethyl E,E,E-pentadeca-2,6,10-trienes functionalized in the 1 and 14 positions.Some of these compounds, such as the ketoester 16 and the ketoaldehyde 17 may prove useful intermediates for the synthesis of the c