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CCC1CCNCC1

CCCN(CCC)C(=O)n1cc(C)c2c1C[C@]1(c3cccc(O)c3)CCN(CC)C[C@H]1C2
Reaction #2958
(±)-trans-Dipropylaminocarbonyl-6-ethyl-8a-(3-hydroxyphenyl)-3-methyl-4,4a,5,6,7,8,8a,9-octahydro-1H-pyrrolo[2,3-g]isoquinoline
DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(C(=O)NCc2ccccc2)[nH]c2c1C[C@@H]1CN(C)CC[C@@]1(c1cccc(O)c1)C2.Cl
Reaction #2964
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCN1CC[C@@]2(c3cccc(O)c3)Cc3[nH]c(C(=O)Nc4ccccc4)c(C)c3C[C@@H]2C1
Reaction #2966
title compound
Ausbeute 22.1%DOI: 10.6084/m9.figshare.5104873.v1
CCCC1CCN(CCOc2cccc(-c3noc4ccsc34)c2)CC1
Reaction #8775
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C1N(Cc2cccc(-c3cccnc3)c2)CCCC12CCN(c1cnc3ccccc3n1)CC2
Reaction #69823
title compound
Ausbeute 46.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(CN2CCCC3(CCN(c4cnc5ccccc5n4)CC3)C2=O)ccn1
Reaction #69847
title compound
Ausbeute 68.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1N(Cc2cccc(I)c2)CCCC12CCN(c1cnc3ccccc3n1)CC2
Reaction #69848
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C1N(Cc2cccc(-n3nccn3)c2)CCCC12CCN(c1cnc3ccccc3n1)CC2
Reaction #69849
title compounds
Ausbeute 30.9%DOI: 10.6084/m9.figshare.5104873.v1
N#CCC1CCN(c2ccc(Cl)nc2)CC1
Reaction #166339
compound 254
Ausbeute 40.2%DOI: 10.6084/m9.figshare.5104873.v1
CCCC1CCN(C(=O)/C=C/c2cnc3c(c2)CCC(=O)N3)CC1
Reaction #170101
title compound
Ausbeute 38.2%DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc2ccccc2n1C1CC2CCC(C1)N2CCC1(c2ccc3c(c2)OCO3)CCN(C(=O)c2ccc(Cl)c(S(N)(=O)=O)c2)CC1
Reaction #177962
DOI: 10.1039/C8SC04228D
Nc1ccc(C#CCCN2CCC(Cc3ccc(Cl)cc3)CC2)cc1
Reaction #184155
DOI: 10.1039/C8SC04228D
CCC(=O)C1(Nc2ccccc2)CCN(CCc2ccccc2)CC1
Reaction #190258
DOI: 10.1039/C8SC04228D
CCCCC1CCN(CCCn2c(=O)oc3c(C(C)C)ccc(C)c32)CC1
Reaction #192152
DOI: 10.1039/C8SC04228D
CC(C)(N)C(=O)NC(Cc1c[nH]c2ccccc12)C(=O)N1CCC2(CC1)CC(N(CC(=O)O)S(C)(=O)=O)c1ccccc12
Reaction #193891
DOI: 10.1039/C8SC04228D
COc1cc(N2CCC(CCS(C)(=O)=O)CC2)c(C)cc1[N+](=O)[O-]
Reaction #197125
DOI: 10.1039/C8SC04228D
CCCN1CCC(CCC(=O)c2cc(Cl)c(N)cc2OC)CC1
Reaction #198653
DOI: 10.1039/C8SC04228D
Nc1cc(OCc2cccc(I)c2)c(C(=O)NC2CN3CCC2CC3)cc1Cl
Reaction #203495
DOI: 10.1039/C8SC04228D
CCCCCCC1CCN(CCCCCO)CC1
Reaction #205012
DOI: 10.1039/C8SC04228D
CCCCC1CCN(CCCn2c(=O)oc3c(F)cc(Br)cc32)CC1
Reaction #208031
DOI: 10.1039/C8SC04228D
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