6789-52-2

Upstream product

• 107-13-1 acrylonitrile 
• 67-64-1 acetone 
• 67-63-0 isopropyl alcohol 

Downstream Products

• 139619-73-1 (1R,3S)-5-[2-[(1R,3aS,6S,7aR)-6-(3,3-Dimethoxy-propyl)-1-((R)-5-hydroxy-1,5-dimethyl-hexyl)-7a-methyl-octahydro-inden-(4E)-ylidene]-eth-(Z)-ylidene]-4-methylene-cyclohexane-1,3-diol 
• 194208-59-8 2-{2-[(3R,3aR,5R,7aR)-7-[(3S,5R)-3,5-Bis-(tert-butyl-dimethyl-silanyloxy)-2-methyl-cyclohex-1-enylethynyl]-3-((R)-5-methoxymethoxy-1,5-dimethyl-hexyl)-3a-methyl-2,3,3a,4,5,7a-hexahydro-1H-inden-5-yl]-ethyl}-[1,3]dioxolane 
• 139619-83-3 2-{2-[(3R,3aR,5S,7aS)-7-[2-[(3S,5R)-3,5-Bis-(tert-butyl-dimethyl-silanyloxy)-2-methylene-cyclohex-(Z)-ylidene]-eth-(E)-ylidene]-3-((R)-5-methoxymethoxy-1,5-dimethyl-hexyl)-3a-methyl-octahydro-inden-5-yl]-ethyl}-[1,3]dioxolane 
• 139619-82-2 2-{2-[(3R,3aR,5R,7aR)-7-{(Z)-2-[(3S,5R)-3,5-Bis-(tert-butyl-dimethyl-silanyloxy)-2-methyl-cyclohex-1-enyl]-vinyl}-3-((R)-5-methoxymethoxy-1,5-dimethyl-hexyl)-3a-methyl-2,3,3a,4,5,7a-hexahydro-1H-inden-5-yl]-ethyl}-[1,3]dioxolane 

Relevant academic research and scientific papers

Tetrabutylammonium decatungstate-photosensitized alkylation of electrophilic alkenes: Convenient functionalization of aliphatic C-H bonds

Tetrabutylammonium decatungstate (TBADT, 2×10-3M) is an effective photocatalyst for the alkylation of electrophilic alkenes (0.1 M, α,β-unsaturated nitriles, esters, ketones) by alkanes, alcohols, and ethers. The products are in most cases obtained in >70% isolated yields, through an experimentally very simple procedure. The kinetics of the radical processes following initial hydrogen abstraction by excited TBADT in deoxygenated MeCN have been studied. In the absence of a trap, back hydrogen transfer from reduced tungstate is the main pathway for alkyl radicals, while α-hydroxyalkyl radicals are oxidized to ketones by ground-state TBADT. With both radical types the reaction ceases at a few percent conversion. However, trapping by electrophilic alkenes is followed by reduction of the radical adduct and regeneration of the catalyst, which allows the alkylation to proceed up to complete alkene conversion with the mentioned good yields of products. With a nucleophilic (α-hydroxyalkyl) radical, alkylation is efficient (Φ = 0.58) and can also be carried out when degassing is omitted, the only difference being a short induction period. With a less reactive (cyclohexyl) radical, the quantum yield is lower (Φ = 0.06) and the reaction is considerably slowed in aerated solutions, but the chemical yield remains good.

Ultrasonic effects on electroorganic processes. Part 22. Cathodic crossed hydrocoupling of acetone with acrylonitrile

The ultrasonic effects on the cathodic-crossed hydrocoupling of acetone with acrylonitrile were examined. The total current efficiency of all products in the cathodic reduction of a mixture of acetone and acrylonitrile was little influenced by ultrasonic