Ähnlichkeitssuche

12155

CC(C)(Oc1ccc(NC(=O)Cc2ccccc2)cc1)C(=O)O
Reaction #3085
2-[4-(phenylacetamido)phenoxy]-2-methyl propionic acid
Ausbeute 57.4%DOI: 10.6084/m9.figshare.5104873.v1
C=C(Cc1ccccc1)C(=O)OCC
Reaction #6176
title compound
Ausbeute 85.0%DOI: 10.6084/m9.figshare.5104873.v1
Reaction #6484
amide
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(Oc1ccc(NC(=O)Cc2ccccc2)cc1)C(=O)O
Reaction #6537
2-[4-(phenylacetamido)phenoxy]-2-methyl propionic acid
Ausbeute 57.4%DOI: 10.6084/m9.figshare.5104873.v1
C=C(Cc1ccccc1)C(=O)O
Reaction #8402
2-methylene-3-phenylpropanoic acid
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1
C=C(Cc1ccccc1)C(=O)O
Reaction #9878
compound 17
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1
Reaction #9879
solid
Ausbeute 83.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCC(N2C(=O)c3cccc(NC(=O)Cc4ccccc4)c3C2=O)C(=O)N1
Reaction #10081
product
Ausbeute 92.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cc1ccccc1)NCc1cccc2c1C(=O)N(C1CCC(=O)NC1=O)C2=O
Reaction #10113
N-{[2-(2,6-dioxo(3-piperidyl))-1,3-dioxoisoindolin-4-yl]methyl}-2-phenylacetamide
Ausbeute 55.0%DOI: 10.6084/m9.figshare.5104873.v1
Cl.c1ccc(Cc2nc3cc4c(cc3o2)C2CNCC4C2)cc1
Reaction #10203
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](NC(=O)Cc1ccccc1)[C@H](Oc1ccc2c(cnn2-c2ccc(F)cc2)c1)c1ccccc1
Reaction #41315
N-[(1R,2S)-1-[1-(4-fluorophenyl)indazol-5-yl]oxy-1-phenyl-propan-2-yl]-2-phenyl-acetamide
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2c(N3CCN(CCc4cccc(NC(=O)Cc5ccccc5)c4)CC3)cccc2n1
Reaction #44069
title compound
Ausbeute 64.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)N(NC(=O)Cc1ccccc1)C(=O)c1ccccc1
Reaction #49912
N'-t-butyl-N-phenylacetyl-N'-benzoylhydrazine
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)N(NC(=O)c1ccccc1)C(=O)Cc1ccccc1
Reaction #49945
N'-t-butyl-N-benzoyl-N'-phenylacetylhydrazine
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cc1ccccc1)c1c[nH]c(C(=O)C(Cl)(Cl)Cl)c1
Reaction #50896
2,2,2-Trichloro-1-(4-phenylacetyl-1H-pyrrol-2-yl)-ethanone
Ausbeute 60.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](NC(=O)Cc1ccccc1)C(=O)O
Reaction #51285
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)COC(=O)C(C)NC(=O)Cc1ccccc1
Reaction #51342
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)COC(=O)[C@H](C)NC(=O)Cc1ccccc1
Reaction #51353
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCC(C)COC(=O)[C@@H](NC(=O)Cc1ccccc1)C(C)C
Reaction #51373
title compound
Ausbeute 136.4%DOI: 10.6084/m9.figshare.5104873.v1
Reaction #55018
47
DOI: 10.6084/m9.figshare.5104873.v1
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