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CC1(CCCNC1)C

O=C(OCC12CCCN(CCC1)C2)c1c[nH]c2ccccc12
Reaction #5482
colorless crystals
Ausbeute 60.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CNCCC1(O)c1ccc(Cl)cc1
Reaction #42975
4-(4-Chloro-phenyl)-3,3-dimethyl-piperidin-4-ol
DOI: 10.6084/m9.figshare.5104873.v1
CN1C(=O)C2CC(c3ccc(N)cc3)(C2)C1=O
Reaction #63349
1-(4-aminophenyl)-3-methyl-3-azabicyclo[3.1.1]heptane-2,4-dione
DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc(C23CC(C2)C(=O)NC3=O)cc1
Reaction #63356
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCN1C(=O)C2CC(c3ccc(NS(C)(=O)=O)cc3)(C2)C1=O
Reaction #63363
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCN1C(=O)C2CC(c3ccc(N)cc3)(C2)C1=O
Reaction #63364
1-(4-aminophenyl)-3-ethyl-3-azabicyclo[3.1.1]heptane-2,4-dione
DOI: 10.6084/m9.figshare.5104873.v1
Cl.O=C1N(Cc2cccc3ccccc23)CCCC12CCNCC2
Reaction #69819
2-(naphthalen-1-ylmethyl)-2,9-diazaspiro[5.5]undecan-1-one hydrochloride
Ausbeute 87.0%DOI: 10.6084/m9.figshare.5104873.v1
Cn1cc(-c2ccc(C34CCCN(CC3)C4)cn2)cn1
Reaction #72734
(−)-5-[2-(1-methyl-1H-pyrazol-4-yl)pyrid-5-yl]-1-azabicyclo[3.2.1]octane
Ausbeute 93.2%DOI: 10.6084/m9.figshare.5104873.v1
c1c[nH]c(-c2ccc(C34CCCN(CC3)C4)cn2)n1
Reaction #72737
(−)-5-[2-(−1H-Imidazol-2-yl)pyrid-5-yl]-1-azabicyclo[3.2.1]octane
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ncccc1C12CCCN(CC1)C2
Reaction #72738
expected product
Ausbeute 76.9%DOI: 10.6084/m9.figshare.5104873.v1
CSC(=S)OC1(c2ccc(Cl)cc2)CCN(Cc2ccccc2)CC1(C)C
Reaction #173474
DOI: 10.1039/C8SC04228D
Cc1cc(CN2CC(c3ccc(F)cc3)C3(CCCNC3)C2=O)no1
Reaction #176345
DOI: 10.1039/C8SC04228D
COC(=O)c1cccc(C(=O)NC(CC(=O)N2CCC(O)(c3ccc(Cl)cc3)C(C)(C)C2)C(C)C)c1
Reaction #177093
DOI: 10.1039/C8SC04228D
CN1CC(c2ccccc2)C2(CCCN(C(=O)C(COCc3ccccc3)NC(=O)OC(C)(C)C)C2)C1=O
Reaction #180210
DOI: 10.1039/C8SC04228D
C=CCC1(C)CC(c2cncc(Cl)c2)C(c2ccc(Cl)cc2)N(C(CC)CO)C1=O
Reaction #180857
DOI: 10.1039/C8SC04228D
CCC1(CC=O)CC(c2cccc(Cl)c2)C(c2ccc(Cl)cc2)N(C(CNS(=O)(=O)C2CC2)C2CC2)C1=O
Reaction #186555
DOI: 10.1039/C8SC04228D
CN1C(=O)CCC2(C)c3ccc(-c4ccc5c(c4)Cc4ccccc4-5)cc3CCC12
Reaction #186629
DOI: 10.1039/C8SC04228D
CC1(CC=O)CC(c2cccc(Cl)c2)C(c2ccc(Cl)cc2)N(C2C=CCC2)C1=O
Reaction #193537
DOI: 10.1039/C8SC04228D
CCOCCn1c(NC2CCN(CCC3(c4ccc(Cl)c(Cl)c4)CCCN(C(=O)c4cc(OC)c(OC)c(OC)c4)C3)CC2)nc2ccccc21
Reaction #196540
DOI: 10.1039/C8SC04228D
Nc1ccc(I)cc1C1NC(=O)CC(c2cccc(Cl)c2)C12C(=O)Nc1cc(Cl)ccc12
Reaction #196723
DOI: 10.1039/C8SC04228D
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