Busqueda de Subestructura

1018693

CO[C@@H]1CNCC[C@@H]1NC(=O)OCc1ccccc1.Cl
Reaction #72029
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(N2CC[C@H](NC(=O)OCc3ccccc3)[C@H](OC)C2)ccn1
Reaction #72030
title compound
Rendimiento 32.3%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cncc(N2CC[C@H](NC(=O)OCc3ccccc3)[C@H](OC)C2)c1
Reaction #72033
title compound
Rendimiento 51.2%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(C)nc(N2CC[C@H](NC(=O)OCc3ccccc3)[C@H](OC)C2)c1
Reaction #72040
title compound
Rendimiento 7.4%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(N2CC[C@H](NC(=O)OCc3ccccc3)[C@H](OC)C2)cc(C)n1
Reaction #72044
title compound
Rendimiento 34.5%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(N2CC[C@H](NC(=O)OCc3ccccc3)[C@H](OC)C2)cnc1C
Reaction #72049
title compound
Rendimiento 86.4%DOI: 10.6084/m9.figshare.5104873.v1
CO[C@@H]1CN(c2cc(C)ncn2)CC[C@@H]1NC(=O)OCc1ccccc1
Reaction #72054
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(F)cc(N2CC[C@H](NC(=O)OCc3ccccc3)[C@H](OC)C2)c1
Reaction #72058
title compound
Rendimiento 34.5%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(N2CC[C@H](NC(=O)OCc3ccccc3)[C@H](OC)C2)ccc1F
Reaction #72061
title compound
Rendimiento 14.4%DOI: 10.6084/m9.figshare.5104873.v1
CO[C@@H]1CN(C(=O)CCl)CC[C@@H]1NC(=O)OCc1ccccc1
Reaction #72091
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(CC(=O)N1CC[C@H](NC(=O)OCc2ccccc2)[C@H](OC)C1)C(C)=O
Reaction #72092
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(CC(=O)N1CCC(NC(=O)OCc2ccccc2)C(OC)C1)C(C)=O
Reaction #1030281
DOI: 10.1039/C8SC04228D
CCOC(=O)c1cncc(N2CC[C@H](NC(=O)OCc3ccccc3)[C@H](OC)C2)c1
Reaction #1512410
title compound
Rendimiento 51.2%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(N2CC[C@H](NC(=O)OCc3ccccc3)[C@H](OC)C2)cnc1C
Reaction #1512423
title compound
Rendimiento 86.4%DOI: 10.6084/m9.figshare.5104873.v1
CO[C@@H]1CN(c2cc(C)ncn2)CC[C@@H]1NC(=O)OCc1ccccc1
Reaction #1512428
Benzyl cis(±)-[3-methoxy-1-(6-methylpyrimidin-4-yl)piperidin-4-yl]carbamate
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(F)cc(N2CC[C@H](NC(=O)OCc3ccccc3)[C@H](OC)C2)c1
Reaction #1512431
title compound
Rendimiento 34.5%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(N2CC[C@H](NC(=O)OCc3ccccc3)[C@H](OC)C2)ccc1F
Reaction #1512434
title compound
Rendimiento 14.4%DOI: 10.6084/m9.figshare.5104873.v1
CO[C@@H]1CN(C(=O)CCl)CC[C@@H]1NC(=O)OCc1ccccc1
Reaction #1512459
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(CC(=O)N1CC[C@H](NC(=O)OCc2ccccc2)[C@H](OC)C1)C(C)=O
Reaction #1512460
title compound
DOI: 10.6084/m9.figshare.5104873.v1