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801479

O=C(O)[C@H]1CN(C(=O)OCc2ccccc2)CCN1c1cc(Cl)c(Cl)cc1[N+](=O)[O-]
Reaction #11904
title compound
Ausbeute 94.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C1CN(C(=O)OCc2ccccc2)CCN1c1c([N+](=O)[O-])ccc(Cl)c1Cl
Reaction #11905
desired product
Ausbeute 43.6%DOI: 10.6084/m9.figshare.5104873.v1
O=C1Nc2ccc(Cl)c(Cl)c2N2CCN(C(=O)OCc3ccccc3)CC12
Reaction #11906
desired product
Ausbeute 50.7%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C1CN(C(=O)OCc2ccccc2)CCN1c1cc(F)c(F)cc1[N+](=O)[O-]
Reaction #11907
title compound
Ausbeute 16.7%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CN(C(=O)OC(C)(C)C)CCN1CCn1c(=O)cc(C)c2ccc(OC)cc21
Reaction #67963
1-tert-butyl 3-ethyl 4-(2-(7-methoxy-4-methyl-2-oxoquinolin-1(2H)-yl)ethyl)piperazine-1,3-dicarboxylate
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1CN(C(=O)OC(C)(C)C)CCN1C(=O)OCc1ccccc1
Reaction #73089
1-benzyl 4-tert-butyl 2-methyl piperazine-1,2,4-tricarboxylate
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #73090
methyl and ethyl esters
DOI: 10.6084/m9.figshare.5104873.v1
O=C1Nc2cc(Cl)c(Cl)cc2N2CCNC[C@H]12
Reaction #77313
title compound
Ausbeute 113.5%DOI: 10.6084/m9.figshare.5104873.v1
O=C1Nc2cc(Cl)c(Cl)cc2N2CCNC[C@@H]12
Reaction #77314
title compound
Ausbeute 120.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C1CN(C(=O)OCc2ccccc2)CCN1c1c([N+](=O)[O-])ccc(Cl)c1Cl
Reaction #77315
desired product
Ausbeute 43.6%DOI: 10.6084/m9.figshare.5104873.v1
O=C1Nc2ccc(Cl)c(Cl)c2N2CCN(C(=O)OCc3ccccc3)CC12
Reaction #77316
desired product
Ausbeute 50.7%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCN2C(=O)OCC2C1
Reaction #157303
desired product
Ausbeute 59.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCN2C(=O)OCC2C1
Reaction #157304
product
Ausbeute 20.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCN(C(=O)OC(C)(C)C)C(C=O)C1
Reaction #157316
desired product
Ausbeute 80.0%DOI: 10.6084/m9.figshare.5104873.v1
Cl.Cl.O=C(Nc1ccccc1)N1CCNCC1COc1cccnc1
Reaction #157328
desired product
Ausbeute 98.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(-c2ccc(NC(=O)N3CCN(C(=O)OC(C)(C)C)CC3COc3cccnc3)cc2)cc1
Reaction #157331
tert-butyl 4-(4′-methoxybiphenyl-4-ylcarbamoyl)-3-((pyridin-3-yloxy)methyl)piperazine-1-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
Cl.Cl.O=C(Nc1nc2ccc(F)cc2s1)N1CCNCC1COc1cccnc1
Reaction #157335
title compound
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc2cc(NC(=O)N3CCNCC3COc3cccnc3)ccc2s1.Cl
Reaction #157339
title compound
Ausbeute 58.0%DOI: 10.6084/m9.figshare.5104873.v1
Cl.Cl.O=C(Nc1ccc(O)cc1)N1CCNCC1COc1cccnc1
Reaction #157344
title compound
Ausbeute 88.0%DOI: 10.6084/m9.figshare.5104873.v1
Cl.Cl.O=C(c1ccc(-c2ccccc2)o1)N1CCNCC1COc1cccnc1
Reaction #157347
desired product
Ausbeute 89.0%DOI: 10.6084/m9.figshare.5104873.v1
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