The reaction begins with the decarboxylation of the cinnamic acid. Decarboxylation is the removal of the carboxyl group (-COOH) from the cinnamic acid, resulting in the formation of the α,β-unsaturated compound. Decarboxylation reactions often require suitable conditions, such as high temperatures or the presence of a decarboxylating reagent.
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(E)-1-methyl-4-(2-(octylsulfonyl)vinyl)benzene
5-methoxy-2-nitrophenylacetaldehyde
benzene
1-Butanone, 3-methyl-1-(4-methylphenyl)-
Copper(I) iodide
n-Tetradecane
tert-butyldimethyl(2-vinylphenoxy)silane
threo-2-Ethyl-3-hydroxy-2-methyl-3-phenylpropanoic acid
(2-(pyridin-2-yloxy)phenyl)(p-tolyl)methanone
(5aS,10aS)-octahydrodipyrrolo[1,2-a:1',2'-d]pyrazine-5,10-dione
1-methyl-4-(prop-1-en-2-ylsulfonyl)benzene
Benzenemethanol, -alpha--methyl-4-(2-methylpropyl)-, acetate (9CI)
5-imino-2-phenyl-5H,11bH-furo[3',2':5,6]-pyrano[3,4-c]chromen-6-amine
(E)-N,N-bis(tert-butoxycarbonyl)-3-(2,3,4,5,6-pentafluorophenyl)prop-2-en-1-amine
n
4,4-Dimethyl-5-[(E)-2-oxo-4-phenyl-but-3-en-(E)-ylidene]-[1,3]dioxolan-2-one
S,S-dimethyl sulfoximine
Silane, (1,1-dimethylethyl)[[4-[2-iodo-6-(2-propenyl)phenoxy]-2-cyclopenten-1-yl ]oxy]dimethyl-, cis-
2-(4-fluorophenyl)-5-methoxybenzo[d]oxazole
4-IODO-2,6-DINITROTOLUENE
3,3,3-trifluoro-1-(4-iodophenyl)propan-1-one
