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COC

CCN(CC)CCNC(=O)Nc1cc(C)c(Oc2ccnc3cc(OC)c(OC)cc23)cc1C
Reaction #199118
DOI: 10.1039/C8SC04228D
O=C(NCC(=O)N1CCC(Oc2cccc(C(F)(F)F)c2)CC1)c1cc(-c2cccc(O)c2)[nH]n1
Reaction #200670
DOI: 10.1039/C8SC04228D
CC(C)(C)NS(=O)(=O)CCc1ccc(NC(=O)c2nc(C#N)cn2COCC[Si](C)(C)C)c(C2=CCCCC2)c1
Reaction #201894
DOI: 10.1039/C8SC04228D
CC(C)C(=O)Nc1cccc(C2CCN(Cc3ccc(-c4ccc(OC(F)(F)F)cc4)o3)CC2)c1
Reaction #204609
DOI: 10.1039/C8SC04228D
CC(C)(C)Oc1ccccc1C=C[N+](=O)[O-]
Reaction #206136
DOI: 10.1039/C8SC04228D
COc1c(NS(C)(=O)=O)cccc1Oc1ccc(F)cc1NC(=O)Nc1nccs1
Reaction #219126
N-{3-[4-Fluoro-2-(3-thiazol-2-yl-ureido)-phenoxy]-2-methoxy-phenyl}-methanesulfonamide
Ausbeute 64.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCOc1c(Cl)cc(CN(O)C=O)cc1Cl
Reaction #222100
DOI: 10.1039/C8SC04228D
O=C(NCC(=O)N1CCC(Oc2cc(F)cc(C(F)(F)F)c2)CC1)c1cn(-c2ccccc2)cn1
Reaction #229019
DOI: 10.1039/C8SC04228D
CCCCCCCCc1ccc(N(Cc2ccc(Oc3ccccc3)cc2)C(=O)Nc2c(C(C)C)cccc2C(C)C)cc1
Reaction #231935
DOI: 10.1039/C8SC04228D
COc1cc2nccc(Oc3cc(C)c(NC(=O)NCCN4CCCC4)cc3C)c2cc1OC
Reaction #234889
DOI: 10.1039/C8SC04228D
Cl
Reaction #235466
DOI: 10.1039/C8SC04228D
CS(=O)(=O)O
Reaction #235543
DOI: 10.1039/C8SC04228D
COc1ccc(C2CCCCC2[N+](=O)[O-])cc1OC
Reaction #247097
DOI: 10.1039/C8SC04228D
CCCCCC(CC(=O)Nc1cc(C(N)=O)ccc1C(C)(C)C)c1ccc(O)cc1OC
Reaction #253762
DOI: 10.1039/C8SC04228D
CNC(=O)C(=NOC)c1ccccc1Oc1cccc(OC(=O)c2ccccc2)c1
Reaction #256593
DOI: 10.1039/C8SC04228D
Cn1cc(C(N)=O)cc1-c1ccnc(Nc2cc(N3CCNCC3)ccc2OC(F)(F)F)n1
Reaction #270088
DOI: 10.1039/C8SC04228D
O=C(c1ccc(F)cc1)c1cn(-c2cccc(-c3ccccc3OC(F)(F)F)c2)cn1
Reaction #270241
DOI: 10.1039/C8SC04228D
CCC(C)Oc1nc(C(F)(F)F)ccc1C=CC(=O)NCc1cc(F)c(NS(C)(=O)=O)c(C#N)c1
Reaction #279171
DOI: 10.1039/C8SC04228D
CC(C)(C)[N+]([O-])=Cc1ccc(OCc2ccccc2)cc1
Reaction #281571
DOI: 10.1039/C8SC04228D
C=Cc1cc(CNC(=O)C=Cc2ccc(C(F)(F)F)nc2Oc2ccccc2)cc(F)c1NS(C)(=O)=O
Reaction #289569
DOI: 10.1039/C8SC04228D
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