Busqueda de Subestructura

765273

O=C(O)[C@H]1CN(C(=O)OCc2ccccc2)CCN1c1cc(Cl)c(Cl)cc1[N+](=O)[O-]
Reaction #11904
title compound
Rendimiento 94.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C1Nc2cc(Cl)c(Cl)cc2N2CCNC[C@H]12
Reaction #77312
title compound
Rendimiento 157.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C1Nc2cc(Cl)c(Cl)cc2N2CCNC[C@H]12
Reaction #77313
title compound
Rendimiento 113.5%DOI: 10.6084/m9.figshare.5104873.v1
O=C1Nc2cc(Cl)c(Cl)cc2N2CCNC[C@@H]12
Reaction #77314
title compound
Rendimiento 120.2%DOI: 10.6084/m9.figshare.5104873.v1
OCCCN1CCN(c2ccc(Cl)c(Cl)c2)CC1
Reaction #92496
compound 7p
DOI: 10.6084/m9.figshare.5104873.v1
Clc1ccc(N2CCN(CCCI)CC2)cc1Cl
Reaction #92497
1-(3,4-dichlorophenyl)-4-(3-iodopropyl)piperazine
DOI: 10.6084/m9.figshare.5104873.v1
O=C1Nc2cc(CN3CCN(c4ccc(Cl)cc4)CC3)cnc2N2CCC[C@@H]12
Reaction #156763
title compound
Rendimiento 40.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1Nc2cc(CN3CCN(c4ccc(Cl)cc4)CC3)cnc2N2CCCCC12
Reaction #156802
title compound
Rendimiento 41.4%DOI: 10.6084/m9.figshare.5104873.v1
O=C1Nc2cc(CN3CCN(c4ccc(Cl)cc4)CC3)cnc2N2CCCC[C@@H]12
Reaction #156808
title compound
Rendimiento 43.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1CC(=O)Nc2cc(CN3CCN(c4ccc(Cl)cc4)CC3)cnc21
Reaction #156827
title compound
Rendimiento 9.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1CN(Cc2ccccc2)c2ncc(CN3CCN(c4ccc(Cl)cc4)CC3)cc2N1
Reaction #156833
title compound
Rendimiento 40.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C1Nc2cc(CN3CCN(c4ccc(Cl)cc4)CC3)cnc2N2CCSCC12
Reaction #156839
title compound
Rendimiento 56.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)N1CC(=O)Nc2cc(CN3CCN(c4ccc(Cl)cc4)CC3)cnc21
Reaction #156853
title compound
Rendimiento 26.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCN2c3ncc(CN4CCN(c5ccc(Cl)cc5)CC4)cc3NC(=O)C2C1
Reaction #156857
title compound
Rendimiento 82.0%DOI: 10.6084/m9.figshare.5104873.v1
COC[C@H](Nc1nc(N2CCN(c3ccc(Cl)cc3)CC2)nc2c1S(=O)CC2)c1nc2ccc(Cl)cc2[nH]1
Reaction #157289
product
Rendimiento 37.8%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](O)[C@H](Nc1nc(N2CCN(c3ccc(Cl)cc3)CC2)nc2c1S(=O)CC2)c1nc2ccc(Cl)cc2[nH]1
Reaction #157290
product
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCN(c2cc(Cl)c(Cl)cc2[N+](=O)[O-])C(CC(=O)O)C1
Reaction #167679
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCN2c3cc(Cl)c(Cl)cc3NCCC2C1
Reaction #167680
tert-butyl 9,10-dichloro-1,2,4a,5,6,7-hexahydrobenzo[b]pyrazino[1,2-d][1,4]diazepine-3(4H)-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(N2CCN(C(=O)Cn3nc(C(F)(F)F)c(Cl)c3C(C)O)CC2)ccc1Cl
Reaction #175287
DOI: 10.1039/C8SC04228D
COc1cc(N2CCN(C(=O)Cn3nc(-c4cccnc4)c(Cl)c3C)CC2)ccc1Cl
Reaction #176822
DOI: 10.1039/C8SC04228D
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