Ähnlichkeitssuche

48362

CCOC(=O)CCCN[C@@H](Cn1c(=O)c(-c2cccc(OC)c2F)c(C)n(Cc2c(F)cccc2C(F)(F)F)c1=O)c1ccccc1
Reaction #56773
1g
Ausbeute 49.5%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(Br)c(=O)n(C[C@H](N)c2ccccc2)c(=O)n1Cc1c(F)cccc1C(F)(F)F
Reaction #56774
2a
DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(-c2ccccc2Cl)c(=O)n(C[C@H](N)c2ccccc2)c(=O)n1Cc1c(F)cccc1C(F)(F)F
Reaction #56775
2b
DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(-c2ccccc2Cl)c(=O)n(C[C@H](NCCCC(=O)O)c2ccccc2)c(=O)n1Cc1c(F)cccc1C(F)(F)F
Reaction #56776
3-[2(R)-{hydroxycarbonylpropyl-amino}-2-phenylethyl]-5-(2-chlorophenyl)-1-[2-fluoro-6-(trifluoromethyl)benzyl]-6-methyl-pyrimidine-2,4(1H,3H)-dione
DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(-c2c(C)n(Cc3c(F)cccc3C(F)(F)F)c(=O)n(C[C@H](NCCCC#N)c3ccccc3)c2=O)c1F
Reaction #56777
compound 3a
Ausbeute 94.0%DOI: 10.6084/m9.figshare.5104873.v1
N[C@@H](Cn1c(=O)c(-c2ccccc2Cl)cn(Cc2c(F)cccc2C(F)(F)F)c1=O)c1ccccc1
Reaction #56784
compound 6f
Ausbeute 100.7%DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(-c2cn(Cc3c(F)cccc3C(F)(F)F)c(=O)n(C[C@H](N)c3ccccc3)c2=O)c1Cl
Reaction #56790
compound 7h
Ausbeute 96.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CCCN[C@@H](Cn1c(=O)c(-c2cccc(OC)c2Cl)cn(Cc2c(F)cccc2C(F)(F)F)c1=O)c1ccccc1
Reaction #56791
compound 7i
Ausbeute 53.4%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CCCNC(Cn1c(=O)c(-c2cccc(OC)c2Cl)cn(Cc2c(F)cccc2C(F)(F)F)c1=O)c1ccccc1
Reaction #243595
DOI: 10.1039/C8SC04228D
Cc1c(Br)c(=O)n(CC(N)c2ccccc2)c(=O)n1Cc1c(F)cccc1C(F)(F)F
Reaction #245876
DOI: 10.1039/C8SC04228D
COc1cccc(-c2cn(Cc3c(F)cccc3C(F)(F)F)c(=O)n(CC(N)c3ccccc3)c2=O)c1Cl
Reaction #289672
DOI: 10.1039/C8SC04228D
Cc1c(-c2ccccc2Cl)c(=O)n(CC(N)c2ccccc2)c(=O)n1Cc1c(F)cccc1C(F)(F)F
Reaction #380295
DOI: 10.1039/C8SC04228D
CCOC(=O)CCCN[C@@H](Cn1c(=O)c(-c2cccc(OC)c2F)c(C)n(Cc2c(F)cccc2C(F)(F)F)c1=O)c1ccccc1
Reaction #434952
1g
Ausbeute 49.5%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(Br)c(=O)n(C[C@H](N)c2ccccc2)c(=O)n1Cc1c(F)cccc1C(F)(F)F
Reaction #434953
2a
DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(-c2ccccc2Cl)c(=O)n(C[C@H](N)c2ccccc2)c(=O)n1Cc1c(F)cccc1C(F)(F)F
Reaction #434954
2b
DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(-c2ccccc2Cl)c(=O)n(C[C@H](NCCCC(=O)O)c2ccccc2)c(=O)n1Cc1c(F)cccc1C(F)(F)F
Reaction #434955
3-[2(R)-{hydroxycarbonylpropyl-amino}-2-phenylethyl]-5-(2-chlorophenyl)-1-[2-fluoro-6-(trifluoromethyl)benzyl]-6-methyl-pyrimidine-2,4(1H,3H)-dione
DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(-c2c(C)n(Cc3c(F)cccc3C(F)(F)F)c(=O)n(C[C@H](NCCCC#N)c3ccccc3)c2=O)c1F
Reaction #434956
compound 3a
Ausbeute 94.0%DOI: 10.6084/m9.figshare.5104873.v1
N[C@@H](Cn1c(=O)c(-c2ccccc2Cl)cn(Cc2c(F)cccc2C(F)(F)F)c1=O)c1ccccc1
Reaction #434964
compound 6f
Ausbeute 100.7%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CCCN[C@@H](Cn1c(=O)c(-c2cccc(OC)c2Cl)cn(Cc2c(F)cccc2C(F)(F)F)c1=O)c1ccccc1
Reaction #434969
compound 7i
Ausbeute 53.4%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CCCN[C@@H](Cn1c(=O)c(N2CCN(Cc3cccc([N+](=O)[O-])c3)CC2)c(C)n(Cc2c(F)cccc2C(F)(F)F)c1=O)c1ccccc1
Reaction #661439
compound
Ausbeute 33.0%DOI: 10.6084/m9.figshare.5104873.v1
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