Recherche de Sous-structure

864653

CN(C(=O)Oc1ccc(Cl)cc1)[C@H]1CC[C@H](O)CC1
Reaction #53822
trans-(4-Hydroxy-cyclohexyl)-methyl-carbamic acid 4-chloro-phenyl ester
Rendement 91.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(C(=O)Oc1ccc(Cl)cc1)[C@H]1CC[C@H](OCCCCBr)CC1
Reaction #53823
trans-[4-(4-Bromo-butoxy)-cyclohexyl]-methyl-carbamic acid 4-chloro-phenyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CN(C(=O)Oc1ccc(Cl)cc1)[C@H]1CC[C@H](OCCCCCBr)CC1
Reaction #53824
trans-[4-(5-Bromo-pentyloxy)-cyclohexyl]-methyl-carbamic acid 4-chloro-phenyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CN(C)CCCCCO[C@H]1CC[C@H]([N+](C)([O-])C(=O)Oc2ccc(Cl)cc2)CC1
Reaction #53895
trans-[4-(5-Dimethylamino-pentyloxy)-cyclohexyl]-methyl-carbamic acid 4-chloro-phenyl ester N-oxide
Rendement 63.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(CCCO)C(=O)CCO[C@H]1CC[C@H](N(C)C(=O)Oc2ccc(Cl)cc2)CC1
Reaction #1150812
trans-(4-{2-[(3-hydroxy-propyl)-methyl-carbamoyl]-ethoxy}-cyclohexyl)-methyl-carbamic acid 4-chloro-phenyl ester
Rendement 49.2%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)CCCCCOC1CCC([N+](C)([O-])C(=O)Oc2ccc(Cl)cc2)CC1
Reaction #1232507
DOI: 10.1039/C8SC04228D
CN(C(=O)Oc1ccc(Cl)cc1)C1CCC(OCCCCCBr)CC1
Reaction #1651464
DOI: 10.1039/C8SC04228D
CN(CCCO)C(=O)CCOC1CCC(N(C)C(=O)Oc2ccc(Cl)cc2)CC1
Reaction #1655334
DOI: 10.1039/C8SC04228D
CN(C(=O)Oc1ccc(Cl)cc1)[C@H]1CC[C@H](O)CC1
Reaction #2144402
trans-(4-Hydroxy-cyclohexyl)-methyl-carbamic acid 4-chloro-phenyl ester
Rendement 91.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(C(=O)Oc1ccc(Cl)cc1)[C@H]1CC[C@H](OCCCCBr)CC1
Reaction #2144403
trans-[4-(4-Bromo-butoxy)-cyclohexyl]-methyl-carbamic acid 4-chloro-phenyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CN(C(=O)Oc1ccc(Cl)cc1)[C@H]1CC[C@H](OCCCCCBr)CC1
Reaction #2144404
trans-[4-(5-Bromo-pentyloxy)-cyclohexyl]-methyl-carbamic acid 4-chloro-phenyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CN(C)CCCCCO[C@H]1CC[C@H]([N+](C)([O-])C(=O)Oc2ccc(Cl)cc2)CC1
Reaction #2144475
trans-[4-(5-Dimethylamino-pentyloxy)-cyclohexyl]-methyl-carbamic acid 4-chloro-phenyl ester N-oxide
Rendement 63.0%DOI: 10.6084/m9.figshare.5104873.v1