a. After the reaction is complete, quench the catalyst by adding a suitable quenching agent or by removing the catalyst through filtration. b. Remove the solvent and any byproducts by evaporation under reduced pressure. c. Purify the product by column chromatography or other suitable methods.
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N,N-dimethyl-4-phenoxybut-2-yn-1-amine
(1E,4E)-1-(3-chlorophenyl)deca-1,4-dien-3-one
(E)-3-(3-chlorophenyl)-N-methoxy-N-methylacrylamide
Silica gel
(S)-1,1-bis-(3,5-dimethoxy-phenyl)-3-methyl-2-[(naphthalen-1-ylmethyl)-amino]-butan-1-ol
C26H22N2O6
dimethyl [(2E,4E)-1-methyl-5-phenyl-3-(triisopropylsiloxy)penta-2,4-dienyl](prop-2-ynyl)malonate
(1R,2S)-1-cyclohexyl-2-methyl-1,3-propanediol
Trifluoro-methanesulfonic acid (2R,4S,5R,2'R,4'S,5'R)-2,2'-diphenyl-5'-trifluoromethanesulfonyloxy-[4,4']bi[[1,3]dioxanyl]-5-yl ester
4-chloro-N-(2,2-dimethylpent-4-enylcarbamoyl)benzenesulfonamide
(-)-Benzal-α-phenyl-ethylamin
(E)-3-isopropoxy-3-phenylprop-1-ene
7-chloro-5-(o-tolyl)-1,6-naphthyridine
(Dimethyl-{1-[1-trimethylsilanyl-meth-(E)-ylidene]-hexyl}-silanyl)-benzene
