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752449

CCS(=O)(=O)Nc1ccc(Oc2ccc(F)cc2F)cc1
Reaction #479645
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(CC(F)(F)F)Nc1ccc(Oc2ccc(F)cc2F)cc1
Reaction #479646
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCS(=O)(=O)N(Cc1cccnc1F)c1ccc(Oc2ccc(F)cc2F)cc1
Reaction #479651
title compound
Ausbeute 53.0%DOI: 10.6084/m9.figshare.5104873.v1
CCS(=O)(=O)Nc1ccc(Oc2ccc(F)cc2F)c(Br)c1
Reaction #605521
title compound
Ausbeute 99.7%DOI: 10.6084/m9.figshare.5104873.v1
CCS(=O)(=O)Nc1ccc(Oc2ccc(F)cc2F)c(-c2cc(F)c(=O)n(C)c2)c1
Reaction #605522
title compound
Ausbeute 35.4%DOI: 10.6084/m9.figshare.5104873.v1
CCS(=O)(=O)Nc1ccc(Oc2ccc(F)cc2F)c(-c2cn(C)c(=O)cc2F)c1
Reaction #605534
N-[4-(2,4-difluorophenoxy)-3-(4-fluoro-1-methyl-6-oxopyridin-3-yl)phenyl]ethanesulfonamide
Ausbeute 72.0%DOI: 10.6084/m9.figshare.5104873.v1
CCS(=O)(=O)Nc1ccc(Oc2ccc(F)cc2F)c(-c2cn(C)c(=O)c3nncn23)c1
Reaction #605619
title compound
Ausbeute 49.3%DOI: 10.6084/m9.figshare.5104873.v1
CCS(=O)(=O)Nc1ccc(Oc2ccc(F)cc2F)c(-c2cn(C)c(=O)c3nc(C)oc23)c1
Reaction #605626
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCS(=O)(=O)Nc1ccc(Oc2ccc(F)cc2F)c(-c2cc(C)c(=O)n(CC3CC3)c2)c1
Reaction #605634
title compound
Ausbeute 28.8%DOI: 10.6084/m9.figshare.5104873.v1
CCS(=O)(=O)Nc1ccc(Oc2ccc(F)cc2F)c(-c2cn(C)c(=O)c3oc(C)cc23)c1
Reaction #605670
title compound
Ausbeute 12.0%DOI: 10.6084/m9.figshare.5104873.v1
Cn1cc(-c2cc(NS(C)(=O)=O)ccc2Oc2ccc(F)cc2F)cc(C2CC2)c1=O
Reaction #605671
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cn1cc(-c2cc(NS(C)(=O)=O)ccc2Oc2ccc(F)cc2F)cc(N2CCCC2)c1=O
Reaction #605673
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCS(=O)(=O)Nc1ccc(Oc2ccc(F)cc2F)c(-c2cc(C#C[Si](C)(C)C)c(=O)n(C)c2)c1
Reaction #605675
title compound
Ausbeute 38.7%DOI: 10.6084/m9.figshare.5104873.v1
CCS(=O)(=O)Nc1ccc(Oc2ccc(F)cc2F)c(-c2cc(OC(F)F)c(=O)n(C)c2)c1
Reaction #605681
title compound
Ausbeute 14.8%DOI: 10.6084/m9.figshare.5104873.v1
CCS(=O)(=O)Nc1ccc(Oc2ccc(F)cc2F)c(-c2cc(OCC(F)(F)F)c(=O)n(C)c2)c1
Reaction #605682
title compound
Ausbeute 11.8%DOI: 10.6084/m9.figshare.5104873.v1
CCS(=O)(=O)Nc1cc(Br)cc(Oc2ccc(F)cc2F)c1
Reaction #605703
title compound
Ausbeute 95.6%DOI: 10.6084/m9.figshare.5104873.v1
CCS(=O)(=O)Nc1cc(Oc2ccc(F)cc2F)cc(-c2cc(C)c(=O)n(C)c2)c1
Reaction #605704
title compound
Ausbeute 94.0%DOI: 10.6084/m9.figshare.5104873.v1
CCS(=O)(=O)Nc1ccc(Oc2ccc(F)cc2F)c(Br)c1
Reaction #662791
title compound
Ausbeute 99.7%DOI: 10.6084/m9.figshare.5104873.v1
CCS(=O)(=O)Nc1ccc(Oc2ccc(F)cc2F)c(-c2cc(F)c(=O)n(C)c2)c1
Reaction #662792
title compound
Ausbeute 35.4%DOI: 10.6084/m9.figshare.5104873.v1
CCS(=O)(=O)Nc1ccc(Oc2ccc(F)cc2F)c(-c2cn(C)c(=O)cc2F)c1
Reaction #662804
N-[4-(2,4-difluorophenoxy)-3-(4-fluoro-1-methyl-6-oxopyridin-3-yl)phenyl]ethanesulfonamide
Ausbeute 72.0%DOI: 10.6084/m9.figshare.5104873.v1
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