Teilstruktursuche

723688

CC1CN(c2ccc(N3CC(CNC(=O)C(F)(F)F)OC3=O)cc2F)CCC1=CC#N
Reaction #181779
DOI: 10.1039/C8SC04228D
CC(=O)N(C)CC1CN(c2ccc(N3CCC(=CC#N)CC3)c(F)c2)C(=O)O1
Reaction #232231
DOI: 10.1039/C8SC04228D
CC(=O)NCC1CN(c2ccc(N3CCC4(CC3)CC4(C#N)C#N)c(F)c2)C(=O)O1
Reaction #302616
DOI: 10.1039/C8SC04228D
CC(C#N)=C1CCN(c2ccc(N3CC(CNC(=O)C(Cl)(Cl)Cl)OC3=O)cc2F)CC1
Reaction #382678
DOI: 10.1039/C8SC04228D
CCC(=O)NCC1CN(c2ccc(N3CCC(=CC#N)CC3)c(F)c2)C(=O)O1
Reaction #386183
DOI: 10.1039/C8SC04228D
CC1CN(c2ccc(N3CC(CNC(=O)CC#N)OC3=O)cc2F)CCC1=CC#N
Reaction #402787
DOI: 10.1039/C8SC04228D
N#CC=C1CCN(c2ccc(N3CC(CNC(=O)C(F)F)OC3=O)cc2F)CC1
Reaction #759164
DOI: 10.1039/C8SC04228D
CCC(=O)NC[C@H]1CN(c2ccc(N3CCC(=CC#N)CC3)c(F)c2)C(=O)O1
Reaction #838103
titled compound
Ausbeute 52.0%DOI: 10.6084/m9.figshare.5104873.v1
N#CC=C1CCN(c2ccc(N3C[C@H](CNC(=O)CO)OC3=O)cc2F)CC1
Reaction #838104
title compound
Ausbeute 70.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N(C)C[C@H]1CN(c2ccc(N3CCC(=CC#N)CC3)c(F)c2)C(=O)O1
Reaction #838105
titled compound
Ausbeute 44.0%DOI: 10.6084/m9.figshare.5104873.v1
N#CC=C1CCN(c2ccc(N3C[C@H](CNC(=O)C(F)F)OC3=O)cc2F)CC1
Reaction #838107
title compound
Ausbeute 48.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1CN(c2ccc(N3C[C@H](CNC(=O)C(F)(F)F)OC3=O)cc2F)CCC1=CC#N
Reaction #838108
title compound
Ausbeute 51.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1CN(c2ccc(N3C[C@H](CNC(=O)CC#N)OC3=O)cc2F)CCC1=CC#N
Reaction #838109
title compound
Ausbeute 81.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C#N)=C1CCN(c2ccc(N3C[C@H](CNC(=O)C(Cl)Cl)OC3=O)cc2F)CC1
Reaction #838111
title compound
Ausbeute 63.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C#N)=C1CCN(c2ccc(N3C[C@H](CNC(=O)C(Cl)(Cl)Cl)OC3=O)cc2F)CC1
Reaction #838112
title compound
Ausbeute 45.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)NC[C@H]1CN(c2ccc(N3CCC(C(C#N)CO)CC3)c(F)c2)C(=O)O1
Reaction #838117
(S)-N-{3-[4-(4-(1-cyano-2-hydroxy-ethyl)-piperidin-1-yl)-3-fluorophenyl]-2-oxo-oxazolidin-5-ylmethyl}-acetamide
Ausbeute 76.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)NC[C@H]1CN(c2ccc(N3CCC4(CC3)CC4(C#N)C#N)c(F)c2)C(=O)O1
Reaction #1113890
title compound
Ausbeute 57.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C#N)=C1CCN(c2ccc(N3CC(CNC(=O)C(Cl)Cl)OC3=O)cc2F)CC1
Reaction #1322224
DOI: 10.1039/C8SC04228D
CC(=O)NC[C@H]1CN(c2ccc(N3CCC4(CC3)CC4(C#N)C#N)c(F)c2)C(=O)O1
Reaction #2334237
title compound
Ausbeute 57.0%DOI: 10.6084/m9.figshare.5104873.v1