Busqueda de Subestructura

11641

COC(=O)c1cc(-c2ccc(OC)c(F)c2)nn(Cc2ccc(F)c(F)c2)c1=O
Reaction #8124
title compound
Rendimiento 92.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(O)Cc1ccc(F)c(F)c1
Reaction #40394
1-(3,4-difluorophenyl)-2-methylpropan-2-ol
DOI: 10.6084/m9.figshare.5104873.v1
Fc1cc(F)c(CN(Cc2cc(F)c(F)cc2F)c2ccc3[nH]cnc3c2)cc1F
Reaction #74215
N,N-Bis(2,4,5-trifluorobenzyl)-1H-benzo[d]imidazol-5-amine
DOI: 10.6084/m9.figshare.5104873.v1
CCc1ccc(CN(Cc2cc(F)c(F)c(F)c2)c2ccc3[nH]cnc3c2)cc1
Reaction #74238
N-(3,4,5-Trifluorobenzyl)-N-(4-ethylbenzyl)-1H-benzo[d]imidazol-5-amine
DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(N(Cc2ccc(F)c(F)c2)C(=O)OC(C)(C)C)sc2ccccc12
Reaction #85427
compound 125-C
Rendimiento 84.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2cc(N(Cc3ccc(F)c(F)c3)S(=O)(=O)c3cccnc3)sc2c1
Reaction #85430
compound 141-G
Rendimiento 66.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(O)(Cc2ccc(F)c(F)c2)CC1
Reaction #88881
title compound
Rendimiento 59.6%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1(Cc2ccc(F)c(F)c2)CCCn2c(-c3ccc(-c4cnc(C)o4)c(OC)c3)nnc21
Reaction #158300
title compound
Rendimiento 92.3%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1(Cc2ccc(F)c(F)c2)CCCNC1=O
Reaction #158326
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1(OCc2ccc(F)c(F)c2)CCCn2c(-c3ccc(-c4cnc(C)o4)c(OC)c3)nnc21
Reaction #158346
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=c1cc(N2CCOCC2)nc2n1CC[C@@H](C(F)(F)F)N2Cc1ccc(F)c(F)c1F
Reaction #167803
(8S)-2-(morpholin-4-yl)-9-(2,3,4-trifluorobenzyl)-8-(trifluoro-methyl)-6,7,8,9-tetrahydro-4H-pyrimido[1,2-a]pyrimidin-4-one
DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccn(Cc2cc(F)c(F)c(F)c2)n1
Reaction #175175
DOI: 10.1039/C8SC04228D
CC1(C)C(C=C(Cl)c2ccc(Cl)cc2)C1C(=O)OC(F)(F)c1ccc(F)c(F)c1F
Reaction #178769
DOI: 10.1039/C8SC04228D
CC(c1ccc(F)c(F)c1)N1CCOC(CNC(=O)OC(C)(C)C)C1
Reaction #184560
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CC(SC(c2ccccc2)(c2ccccc2)c2ccccc2)CC1COCc1cc(F)c(F)cc1F
Reaction #196119
DOI: 10.1039/C8SC04228D
COC1=N[C@H](Cc2cc(F)c(F)cc2F)C(OC)=N[C@H]1C(C)C
Reaction #220012
title compound
Rendimiento 62.7%DOI: 10.6084/m9.figshare.5104873.v1
Fc1cc(Br)c(CBr)cc1F
Reaction #220014
2-bromo-4,5-difluorobenzyl bromide
Rendimiento 120.7%DOI: 10.6084/m9.figshare.5104873.v1
COC1=N[C@H](Cc2cc(F)c(F)cc2F)C(OC)=N[C@H]1C(C)C
Reaction #220240
title compound
Rendimiento 62.7%DOI: 10.6084/m9.figshare.5104873.v1
Fc1cc(Br)c(CBr)cc1F
Reaction #220242
2-bromo-4,5-difluorobenzyl bromide
Rendimiento 120.7%DOI: 10.6084/m9.figshare.5104873.v1
COC1=NC(C(C)C)C(OC)=NC1Cc1cc(F)c(F)cc1F
Reaction #222755
DOI: 10.1039/C8SC04228D
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