Recherche de Sous-structure

OB(O)c1ccc(C(F)(F)F)cc1

Oc1ccc2nc(-c3ccc(O)c(F)c3)cc(-c3ccc(C(F)(F)F)cc3)c2c1
Reaction #7346
2-(3-Fluoro-4-hydroxyphenyl)-4-(4-trifluoromethylphenyl)quinolin-6-ol
Rendement 76.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(Cc1c[nH]c2c(-c3ccc(C(F)(F)F)cc3)cccc12)NC(=O)OC(C)(C)C
Reaction #8188
{1,1-dimethyl-2-[7-(4-trifluoromethyl-phenyl)-1 H-indol-3-yl]-ethyl}-carbamic acid tert-butyl ester
Rendement 93.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(Cc1c[nH]c2c(-c3ccc(C(F)(F)F)cc3C(F)(F)F)cccc12)NC(=O)OC(C)(C)C
Reaction #8191
{2-[7-(2,4-Bis-trifluoromethyl-phenyl)-1H-indol-3-yl]-1,1-dimethyl-ethyl}-carbamic acid tert-butyl ester
Rendement 89.2%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)COc1ccc(OCc2cc(-c3ccc(C(F)(F)F)cc3)cc(-c3ccc(C(F)(F)F)cc3)c2)cc1C
Reaction #47779
[4-(3,5-bis(4-trifluoromethylphenyl)-benzyloxy)-2-methyl-phenoxy]-acetic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)N1CCC(Oc2ccc3c(c2)cc(C(=O)N2CCC(F)(F)CC2)n3-c2ccc(C(F)(F)F)cc2)CC1
Reaction #48135
title compound
DOI: 10.6084/m9.figshare.5104873.v1
FC(F)(F)c1ccc(-c2cccc(SC3CCCC3)c2)cc1
Reaction #53562
[3-(4-trifluoromethylphenyl)phenyl] cyclopentyl sulfide
Rendement 78.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1NCCc2c(-c3ccc(C(F)(F)F)cc3)[nH]c3cccc1c23
Reaction #61576
2-(4-trifluoromethyl-phenyl)-1,3,4,5-tetrahydro-azepino[5,4,3-cd]indol-6-one
DOI: 10.6084/m9.figshare.5104873.v1
O=Cc1ccc(-c2ccc(C(F)(F)F)cc2)cn1
Reaction #61756
5-(4-trifluoromethyl-phenyl)-pyridine-2-carbaldehyde
Rendement 66.7%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cncc(-c2ccc(C(F)(F)F)cc2)c1
Reaction #61798
5-(4-Trifluoromethyl-phenyl)-nicotinic acid methyl ester
Rendement 76.8%DOI: 10.6084/m9.figshare.5104873.v1
CSc1ccc(C2=C(c3ccc(C(F)(F)F)cc3)CCC2)cc1
Reaction #65803
1-[2-(4-trifluoromethylphenyl)cyclopenten-1-yl]-4-(methylthio)benzene
Rendement 81.0%DOI: 10.6084/m9.figshare.5104873.v1
FC(F)(F)c1ccc(-c2ccc(N3CCCN(c4ccc(-c5ccc(C(F)(F)F)cc5)cn4)CC3)nc2)cc1
Reaction #77570
title compound
Rendement 40.6%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cccnc1-c1ccc(C(F)(F)F)cc1
Reaction #80193
brown oil
Rendement 109.7%DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCOc2cc(-c3ccc(C(F)(F)F)cc3)ccc21
Reaction #91898
title compound
Rendement 64.5%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H](OC(C)(C)C)c1c(C)nc2sc3c(c2c1-c1ccc(C(F)(F)F)cc1)CCCC3
Reaction #92243
title compound
Rendement 72.7%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(B2OCC(C)(C)CO2)ccc1C(F)(F)F
Reaction #157742
title compound
Rendement 62.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C#N)(Cn1nc2cc(Cl)cc(-c3ccc(C(F)(F)F)cc3)c2n1)NC(=O)c1ccc(OC(F)(F)F)cc1
Reaction #158151
title compound
DOI: 10.6084/m9.figshare.5104873.v1
FC(F)(F)c1ccc(-c2cncc(N3CC4CC5CC3CN(C5)C4)c2)cc1
Reaction #167612
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cccc2sc(-c3ccc(C(F)(F)F)cc3)nc12
Reaction #173501
DOI: 10.1039/C8SC04228D
CNc1ncnn2c(C)nc(-c3cnn(C)c3-c3ccc(C(F)(F)F)cc3)c12
Reaction #175603
DOI: 10.1039/C8SC04228D
CC1C(c2cc(C(F)(F)F)cc(C(F)(F)F)c2)OC(=O)N1Cc1cc(C(F)(F)F)ccc1-c1nc(Br)cs1
Reaction #177041
DOI: 10.1039/C8SC04228D
Page 1Suivant