部分構造検索

C1CN2CCC1CC2

CCCOc1ccccc1C(=O)NC1CN2CCC1CC2.Cl
Reaction #3858
N-(1-Azabicyclo[2.2.2]oct-3-yl)-2-propoxybenzamide, hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
OC1C2CCN(CC2)C1C(c1ccccc1)c1ccccc1
Reaction #5069
2-(Diphenylmethyl)-1-azabicyclo[2.2.2]octan-3-ol
DOI: 10.6084/m9.figshare.5104873.v1
Cl.O=C(N[C@H]1CN2CCC1CC2)c1cc2cc(Cl)cc(Cl)c2o1
Reaction #43732
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(N[C@H]1CN2CCC1CC2)c1cc2cc(F)cc(F)c2o1
Reaction #43742
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(N[C@H]1CN2CCC1CC2)c1cc2cc(F)cc(Br)c2o1
Reaction #43743
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(N[C@H]1CN2CCC1CC2)c1cc2cccc(Br)c2o1
Reaction #43744
title compound
DOI: 10.6084/m9.figshare.5104873.v1
OC1(CS)CN2CCC1CC2
Reaction #163565
3-hydroxy-3-mercaptomethylquinuclidine
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(C)SCC1(O)CN2CCC1CC2.O=C(O)c1ccccc1
Reaction #163566
3-hydroxy-3-[(1-ethoxyethyl)mercaptomethyl]quinuclidine benzoic acid salt
収率 69.5%DOI: 10.6084/m9.figshare.5104873.v1
Cl.Cl.NC(C(=O)O[C@H]1CN2CCC1CC2)c1ccccc1
Reaction #164158
(R)-quinuclidin-3-yl 2-amino-2-phenylacetate di-hydrochloride
収率 97.0%DOI: 10.6084/m9.figshare.5104873.v1
N=C(NC(=O)c1nc(Cl)c(N)nc1N)NC1CN2CCC1CC2
Reaction #164689
title compound
収率 15.1%DOI: 10.6084/m9.figshare.5104873.v1
NC(=NC(=O)c1nc(Cl)c(N)nc1N)NC1C[N+]2(CC(=O)O)CCC1CC2.[Br-]
Reaction #164698
title compound
収率 16.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(C[N+]23CCC(CC2)C(NC(N)=NC(=O)c2nc(Cl)c(N)nc2N)C3)cc(OC)c1OC.[Cl-]
Reaction #164699
title compound
収率 42.0%DOI: 10.6084/m9.figshare.5104873.v1
NC(=NC(=O)c1nc(Cl)c(N)nc1N)NC1C[N+]2(Cc3ccccc3)CCC1CC2.[Br-]
Reaction #164700
title compound
収率 57.3%DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc2c(C(=O)NC3CN4CCC3CC4)cccc2o1
Reaction #181019
DOI: 10.1039/C8SC04228D
c1ccc(Nc2ccc(-c3ccc(OC4CN5CCC4CC5)cc3)cc2)cc1
Reaction #181977
DOI: 10.1039/C8SC04228D
COc1ccccc1CN=C1C(=Cc2ccccc2)N2CCC1CC2
Reaction #183254
DOI: 10.1039/C8SC04228D
COc1ccccc1C(=O)NC1CN2CCC1CC2
Reaction #185759
DOI: 10.1039/C8SC04228D
O=C(NC1CN2CCC1CC2)c1cc2ccc(C#CCO)cc2o1
Reaction #190670
DOI: 10.1039/C8SC04228D
CC12CCN(CC1)CC2C(=O)NC1CCN(CCc2ccccc2)C1
Reaction #192803
DOI: 10.1039/C8SC04228D
OC1C2CCN(CC2)C1CN1CCCCC1
Reaction #198992
DOI: 10.1039/C8SC04228D
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