76126-87-9

Upstream product

• 1541-10-2 mesitylthiol 
• 106-95-6 allyl bromide 
• 576-83-0 2,4,6-trimethylphenyl bromide 

Downstream Products

• 78012-54-1 3-(2,4,6-trimethylphenylsulfinyl)prop-1-ene 
• 78012-57-4 1-phenyl-2-(2,4,6-trimethylphenylsulfinyl)but-3-en-1-ol 
• 78012-62-1 (E)-1-phenyl-4-(2,4,6-trimethylphenylsulfinyl)but-3-en-1-ol 
• 112-88-9 octadec-1-ene 
• 89025-53-6 n-pentadecyl-2'-pyridylsulphide 
• 76120-48-4 1-phenyl-2-(2,4,6-trimethylphenylthio)but-3-en-1-ol 
• 76120-49-5 (Z)-1-phenyl-4-(2,4,6-trimethylphenylthio)but-3-en-1-ol 
• 76120-50-8 (E)-1-phenyl-4-(2,4,6-trimethylphenylsulfinyl)but-3-en-1-ol 

Relevant academic research and scientific papers

Lewis acid mediated reactions of allyl chalcogenides with ethyl glyoxylate

Allyl mesityl sulfide reacted with ethyl glyoxylate in the presence of tin(IV) chloride to give a tetrahydrofuran derivative. The presence of a bulky substituent on the sulfur atom was crucial to the present reaction. The reaction of allyl mesityl selenid

Regio- and Stereo-selectivity in the Reactions of Anions of Aryl Allyl Sulfides with Benzaldehyde

Addition reactions of anions of aryl allyl sulfides to benzaldehyde proceed readily and in good yields and afford mixtures of products resulting from α- and γ-attack on the allyl anion. γ-Products predominate, and the ratio of (E):(Z) isomers usually surrounds unity, although in the case of the reaction involving 3-(phenylthio)but-1-ene the ratio is 10:1.The ratio of diastereoisomers formed in products resulting from α-attack ranges from 3:1 to 1.3:1 (starting from 3-(2,4,6-trimethyl-phenylthio)prop-1-ene and 2-methyl-3-(phenylthio)prop-1-ene respectively).