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O=C(O)c1ccccc1-c1ccc(C(F)(F)F)cc1

O=C(Cl)c1ccccc1-c1ccc(C(F)(F)F)cc1
Reaction #80183
title product
Ausbeute 99.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cl)c1ccccc1-c1ccc(C(F)(F)F)cc1
Reaction #80242
4′-Trifluoromethyl-biphenyl-2-carbonyl chloride
DOI: 10.6084/m9.figshare.5104873.v1
O=C(NC1CCN(Cc2ccccc2)CC1)c1ccccc1-c1ccc(C(F)(F)F)cc1
Reaction #177760
DOI: 10.1039/C8SC04228D
N#Cc1cccc(CN2CCN(c3ccc(NC(=O)c4ccccc4-c4ccc(C(F)(F)F)cc4)cc3)CC2)c1
Reaction #226172
DOI: 10.1039/C8SC04228D
O=C(Cl)c1ccccc1-c1ccc(C(F)(F)F)cc1
Reaction #237788
DOI: 10.1039/C8SC04228D
O=C(O)c1ccc(Cl)cc1-c1ccc(C(F)(F)F)cc1
Reaction #262061
DOI: 10.1039/C8SC04228D
O=C(O)c1ccccc1-c1ccc(C(F)(F)F)cc1
Reaction #278758
DOI: 10.1039/C8SC04228D
NC(=O)C1CCN(C(=O)c2ccccc2-c2ccc(C(F)(F)F)cc2)CC1
Reaction #297769
DOI: 10.1039/C8SC04228D
Cc1cccc(C(=O)O)c1-c1ccc(C(F)(F)F)cc1
Reaction #301878
DOI: 10.1039/C8SC04228D
O=C(c1ccccc1-c1ccc(C(F)(F)F)cc1)N1CC2CN(c3cnc4ccccc4n3)CC2C1
Reaction #331180
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccccc1-c1ccc(C(F)(F)F)cc1)N1CC2CN(c3nccc(-c4ccccc4)n3)CC2C1
Reaction #331182
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C(=O)O)c(-c2ccc(C(F)(F)F)cc2)c1
Reaction #372125
DOI: 10.1039/C8SC04228D
O=C(Cl)c1ccccc1-c1ccc(C(F)(F)F)cc1
Reaction #382041
DOI: 10.1039/C8SC04228D
O=C(Cl)c1ccccc1-c1ccc(C(F)(F)F)cc1
Reaction #518536
4′-Trifluoromethyl-biphenyl-2-carbonyl chloride
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cc2cc(NC(=O)c3ccccc3-c3ccc(C(F)(F)F)cc3)ccc2n1CC
Reaction #577171
title compound
Ausbeute 54.4%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cl)c1ccccc1-c1ccc(C(F)(F)F)cc1
Reaction #577179
4′-(trifluoromethyl)[1,1′-biphenyl]-2-carbonyl chloride
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1c(Cl)c2cc(NC(=O)c3ccccc3-c3ccc(C(F)(F)F)cc3)ccc2n1C
Reaction #577186
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(c1ccccc1)C1CCN(c2ccc(NC(=O)c3ccccc3-c3ccc(C(F)(F)F)cc3)cc2)CC1
Reaction #578051
methyl α-phenyl-1-[4-[[[4′-(trifluoromethyl)-[1,1′-biphenyl]-2-yl]carbonyl]amino]phenyl]-4-piperidineacetate
Ausbeute 77.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cl)c1ccccc1-c1ccc(C(F)(F)F)cc1
Reaction #581562
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc(NC(=O)c2ccccc2-c2ccc(C(F)(F)F)cc2)cc1
Reaction #581579
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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