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511409

CC1CC(n2cnc3c(N)ncnc32)C1CO
Reaction #6051
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)N1CCC(COCC(NC(=O)c2cc3ccc(Cl)cc3s2)c2ccccc2Cl)CC1
Reaction #60709
6-Chloro-N-[1-(2-chlorophenyl)-2-(1-isopropylpiperidin-4-yl-methoxy)ethyl]benzo[b]thiophene-2-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1
c1ccc(CN2C3CCC2CC2(CO2)C3)cc1
Reaction #68978
8-Benzyl-spiro[8-azabicyclo[3.2.1]octane-3,2′-oxirane]
DOI: 10.6084/m9.figshare.5104873.v1
CN([C@@H]1CC[C@H](COCc2ccccc2)C1)S(=O)(=O)c1ccc(Cl)nc1
Reaction #73535
N-{(1R,3S)-3-[(benzyloxy)methyl]cyclopentyl}-6-chloro-N-methylpyridine-3-sulfonamide
Ausbeute 86.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CNc2nnc(N3CCC(O)(CO)CC3)c3ccc(C#N)cc23)cc1Cl.Cl
Reaction #75615
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Brc1cnc2c(c1)CC1(CN3CCC1CC3)O2
Reaction #76784
title compound
Ausbeute 81.0%DOI: 10.6084/m9.figshare.5104873.v1
c1ccc(-c2cnc3c(c2)CC2(CN4CCC2CC4)O3)cc1
Reaction #76785
title compound
Ausbeute 68.5%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1cnc2c(c1)CC1(CN3CCC1CC3)O2
Reaction #76786
title compound
Ausbeute 51.0%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1cnc2c(c1)C[C@@]1(CN3CCC1CC3)O2
Reaction #76787
title compound
Ausbeute 98.6%DOI: 10.6084/m9.figshare.5104873.v1
C#Cc1cnc2c(c1)C[C@@]1(CN3CCC1CC3)O2
Reaction #76796
title compound
Ausbeute 59.0%DOI: 10.6084/m9.figshare.5104873.v1
c1coc(-c2cnc3c(c2)CC2(CN4CCC2CC4)O3)c1
Reaction #76797
title compound
Ausbeute 89.2%DOI: 10.6084/m9.figshare.5104873.v1
c1cncc(-c2cnc3c(c2)CC2(CN4CCC2CC4)O3)c1
Reaction #76798
title compound
Ausbeute 37.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cnc2c(c1)CC1(CN3CCC1CC3)O2
Reaction #76799
title compound
Ausbeute 166.3%DOI: 10.6084/m9.figshare.5104873.v1
C=Cc1cnc2c(c1)CC1(CN3CCC1CC3)O2
Reaction #76800
title compound
Ausbeute 186.9%DOI: 10.6084/m9.figshare.5104873.v1
Fc1ccc2c(n1)OC1(C2)CN2CCC1CC2
Reaction #76807
sub-title compound
Ausbeute 8.0%DOI: 10.6084/m9.figshare.5104873.v1
Brc1cnc2c(c1)CC1(CN3CCC1CC3)O2
Reaction #77881
title compound
Ausbeute 81.0%DOI: 10.6084/m9.figshare.5104873.v1
c1ccc(-c2cnc3c(c2)CC2(CN4CCC2CC4)O3)cc1
Reaction #77882
title compound
Ausbeute 68.5%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1cnc2c(c1)CC1(CN3CCC1CC3)O2
Reaction #77883
title compound
Ausbeute 51.0%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1cnc2c(c1)C[C@@]1(CN3CCC1CC3)O2
Reaction #77884
title compound
Ausbeute 98.6%DOI: 10.6084/m9.figshare.5104873.v1
C#Cc1cnc2c(c1)C[C@@]1(CN3CCC1CC3)O2
Reaction #77894
title compound
Ausbeute 59.0%DOI: 10.6084/m9.figshare.5104873.v1
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