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Oc1cccc(-n2ccnc2)c1

COC(=O)c1cc([N+](=O)[O-])c(-n2ccnc2C2CCCCC2)cc1OC
Reaction #159942
title compound
Ausbeute 100.7%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(N)c(-n2ccnc2C2CCCCC2)cc1OC
Reaction #159943
title compound
Ausbeute 73.7%DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(-n2c(C)nc3cc(-c4nc5ccccc5o4)ccc32)c1
Reaction #161383
title compound
Ausbeute 29.3%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-n2c(C(C)(C)c3ccc(S(N)(=O)=O)c(Cl)c3)cnc2S)ccc1F
Reaction #171056
title compound
Ausbeute 82.4%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-n2c(C(C)(C)c3ccc(F)c(C#N)c3)cnc2S)ccc1F
Reaction #171067
2-fluoro-5-(2-(1-(4-fluoro-3-methoxyphenyl)-2-mercapto-1H-imidazol-5-yl)propan-2-yl)benzonitrile
Ausbeute 65.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)n1c(=O)n(-c2ccc3c(c2)OCO3)c2ncccc21
Reaction #181103
DOI: 10.1039/C8SC04228D
CNc1nnc(-c2ccc3ncn(-c4cccc(OC(F)(F)F)c4)c3c2)o1
Reaction #191259
DOI: 10.1039/C8SC04228D
COC(=O)c1ccc(-n2ccnc2)cc1OCc1ccccc1
Reaction #209545
DOI: 10.1039/C8SC04228D
COC(=O)c1cc([N+](=O)[O-])c(-n2ccnc2C2CCCCC2)cc1OC
Reaction #209919
DOI: 10.1039/C8SC04228D
Oc1cccc(-n2cnc(-c3ccccc3)c2)c1
Reaction #225928
DOI: 10.1039/C8SC04228D
C=CCn1c(=O)n(-c2ccc3c(c2)OCO3)c2nc(F)ccc21
Reaction #227447
DOI: 10.1039/C8SC04228D
CCOc1cccc(-n2cc(C(=O)N3CCNCC3COC(C)=O)nc2-c2ccc(C)cc2)c1
Reaction #230974
DOI: 10.1039/C8SC04228D
COc1cc(Cl)c(-n2c(=O)[nH]c3cnc(C(N)=O)nc32)cc1OCc1c(OC)ccc(F)c1F
Reaction #238826
DOI: 10.1039/C8SC04228D
CC(C)Oc1cccc2c1C1=NCCN1c1c(-c3noc(C4CC4)n3)ncn1-2
Reaction #239013
DOI: 10.1039/C8SC04228D
CS(=O)(=O)Nc1ccc(CCN2CCOc3ccc(-n4ccnc4)cc3OCC2)cc1
Reaction #243483
DOI: 10.1039/C8SC04228D
O=c1n(CO)c2cccnc2n1-c1ccc2c(c1)OCO2
Reaction #276600
DOI: 10.1039/C8SC04228D
COc1cc(Cl)c(-n2c(=O)[nH]c3cnc(C(=O)O)nc32)cc1OCc1c(OC)ccc(F)c1F
Reaction #284358
DOI: 10.1039/C8SC04228D
Oc1cccc(-n2cnc3cc(C(F)(F)F)ccc32)c1
Reaction #292230
DOI: 10.1039/C8SC04228D
Cl
Reaction #292337
DOI: 10.1039/C8SC04228D
c1cn(-c2ccc3c(c2)OCCNCCO3)cn1
Reaction #295232
DOI: 10.1039/C8SC04228D
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