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1377828

O=C(O)c1ccc(-c2cccc(F)c2)nc1
Reaction #208441
DOI: 10.1039/C8SC04228D
O=C(O)c1ccc(-c2cc(F)ccc2F)nc1
Reaction #210341
DOI: 10.1039/C8SC04228D
CCOC(=O)N1CCC(NC(=O)c2ccc(-c3cc(F)cc(F)c3)nc2)CC1
Reaction #234138
DOI: 10.1039/C8SC04228D
O=C(NC1CCN(CC(F)(F)F)CC1)c1ccc(-c2cc(F)cc(F)c2)nc1
Reaction #234150
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)c1ccc(-c2cc(F)ccc2F)nc1
Reaction #290997
DOI: 10.1039/C8SC04228D
O=C(O)c1ccc(-c2cc(F)ccc2O)nc1
Reaction #297139
DOI: 10.1039/C8SC04228D
CCC(CC)NC(=O)c1ccc(-c2cc(C(=O)NC3CC3)cc(F)c2C)nc1
Reaction #390594
DOI: 10.1039/C8SC04228D
O=C(O)c1ccc(-c2ccc(F)c(F)c2)nc1
Reaction #578750
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1ccc(-c2cccc(F)c2F)nc1
Reaction #578751
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc(-c2cccc(F)c2)nc1C
Reaction #581363
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc(-c2cccc(F)c2F)nc1C
Reaction #581364
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc(-c2ccc(F)c(F)c2)nc1C
Reaction #581391
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc(-c2cccc(F)c2)ccc1C(=O)Nc1ccc2c(c1)NCCC2
Reaction #581412
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc(-c2cccc(F)c2F)ccc1C(=O)Nc1ccc2c(c1)NCCC2
Reaction #581413
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1ccc2cccnc2c1)c1ccc(-c2cccc(F)c2)nc1
Reaction #581451
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc(-c2cccc(F)c2)ccc1C(=O)Nc1ccc2cccnc2c1
Reaction #581463
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc(-c2cccc(F)c2F)ccc1C(=O)Nc1ccc2cccnc2c1
Reaction #581464
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc(-c2ccc(F)c(F)c2)ccc1C(=O)Nc1ccc2c(c1)NCCC2
Reaction #581476
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cl)c1ccc(-c2cccc(F)c2)nc1
Reaction #621924
6-(3-fluorophenyl)-3-pyridinecarbonyl chloride
Ausbeute 99.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NC1CCN(CC(F)(F)F)CC1)c1ccc(-c2cccc(F)c2)nc1
Reaction #689256
desired product
Ausbeute 152.2%DOI: 10.6084/m9.figshare.5104873.v1
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