반응 #364839

ord-ee6776db180d46219c8cd1b78d0330a2

반응 방정식

CC(C)C[C@H](N)C(=O)O
L-leucine
CC[C@H](C)[C@H](N)C(=O)O
L-isoleucine
COc1ccc(C[C@H](N)C(=O)O)cc1
O-methyl-L-tyrosine
N[C@@H](Cc1c[nH]c2ccccc12)C(=O)O
L-tryptophan
[Na+].[OH-]
sodium hydroxide
N[C@@H](Cc1ccccc1)C(=O)O
L-phenylalanine
CC(=O)c1ccccc1
acetophenone

반응 조건

상세 조건
See reaction.notes.procedure_details.

실험 절차

200 μl (50 μmol) of a 0.25 M solution of each of the isatins listed in Table 1, in dioxane; 200 μl (50 μmol) of a 0.25 M solution of the α-amino acids listed in Table 2, in water (including 1 equivalent of sodium hydroxide for the L-phenylalanine, L-leucine, O-benzyl-(D,L)-serine, L-tryptophan, L-isoleucine, and O-methyl-L-tyrosine); and 400 μl (50 μmol) of a 0.125 M solution containing the chalcones produced by reaction of the arylaldehydes and acetophenone compounds of Tables 3 and 4, in dioxane, were combined in 1 ml perfume vials. The vials were capped and heated at 80° C. overnight. The solvent was then evaporated under reduced pressure and the resulting products were all recovered in greater than 85% purity according to high pressure liquid chromatography (HPLC) and mass spectroscopy (MS) experiments.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US06358750B1uspto-grants-2002_03