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c1ccc2c(c1)CCN2

N#Cc1cc(F)cc(-c2cc(Br)c3c(c2)C2(CCCCC2)C(=O)N3)c1
Reaction #7100
title compound
Ausbeute 43.0%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(-c2ccc3c(c2)C2(CCCCC2)C(=O)N3)cc1F
Reaction #7103
title compound
Ausbeute 37.0%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cc(-c2ccc3c(c2)C2(CCCC2)C(=O)N3)ccc1F
Reaction #7110
title compound
Ausbeute 10.5%DOI: 10.6084/m9.figshare.5104873.v1
O=C1Nc2ccc(-c3ccc(F)c(Cl)c3)cc2C12CCCC2
Reaction #7111
title compound
Ausbeute 66.4%DOI: 10.6084/m9.figshare.5104873.v1
Clc1cccc(Nc2cc3c4c(c2)[C@@H]2CNCC[C@@H]2N4CCSC3)c1Cl
Reaction #51543
title compound
DOI: 10.6084/m9.figshare.5104873.v1
FC(F)(F)c1ccc(Cl)c(Nc2cc3c4c(c2)[C@@H]2CNCC[C@@H]2N4CCSC3)c1
Reaction #51544
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(Nc2cc3c4c(c2)[C@@H]2CNCC[C@@H]2N4CCOC3)c(C(C)O)c1
Reaction #51550
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(Nc2cc3c4c(c2)[C@@H]2CNCC[C@@H]2N4CCOC3)c(C(C)=O)c1
Reaction #51551
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)c1cc(Cl)ccc1Nc1cc2c3c(c1)[C@@H]1CNCC[C@@H]1N3CCSC2
Reaction #51562
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C1CC2(C(=O)N1)C(=O)N1CCOc3cc(Cl)cc2c31
Reaction #63258
8'-Chloro-2',3'-dihydrospiro[pyrrolidine-3,6'(5'H)-pyrrolo[1,2,3-de][1,4]benzoxazine]-2,5,5'-trione
DOI: 10.6084/m9.figshare.5104873.v1
Clc1cccc(Nc2cc3c4c(c2)[C@@H]2CNCC[C@@H]2N4CCSC3)c1Cl
Reaction #75825
title compound
DOI: 10.6084/m9.figshare.5104873.v1
FC(F)(F)c1ccc(Cl)c(Nc2cc3c4c(c2)[C@@H]2CNCC[C@@H]2N4CCSC3)c1
Reaction #75826
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(Nc2cc3c4c(c2)[C@@H]2CNCC[C@@H]2N4CCOC3)c(C(C)O)c1
Reaction #75832
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(Nc2cc3c4c(c2)[C@@H]2CNCC[C@@H]2N4CCOC3)c(C(C)=O)c1
Reaction #75833
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CN1CC[C@H]2[C@@H](C1)c1cc(-c3c(F)cccc3F)cc3c1N2CCC3
Reaction #79306
title compound
Ausbeute 62.7%DOI: 10.6084/m9.figshare.5104873.v1
CCC1N(c2ccc(Cl)cc2)c2ccccc2C12CCN(C)CC2
Reaction #95489
1-(4-chlorophenyl)-2-ethyl-1'-methylspiro[indoline-3,4'-piperidine]
DOI: 10.6084/m9.figshare.5104873.v1
CCN1C(=O)C(C)(C)C(=O)N(C)c2cc(OCCCN3C(=O)Cc4ccccc43)ccc21
Reaction #156246
title compound
Ausbeute 61.9%DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2ccccc2C(=O)N1CCN1C(=O)C(CO)(c2cc3c(cc2O)OCO3)c2ccccc21
Reaction #179997
DOI: 10.1039/C8SC04228D
CC(C)(C)CC1NC(C(=O)Nc2ccc(C#N)cc2F)C(c2cccc(Cl)c2F)C12C(=O)Nc1cc(Cl)ccc12
Reaction #181267
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)CCN1C(=O)C2(CC(=O)N(Cc3ccccc3)C2=O)c2cc(Cl)ccc21
Reaction #182222
DOI: 10.1039/C8SC04228D
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