Busqueda de Subestructura

1100449

COC(=O)C(Oc1ccc(C)cc1Cl)c1ccccc1
Reaction #65504
title compound
Rendimiento 83.1%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(Oc1ccc(CBr)cc1Cl)c1ccccc1
Reaction #65505
title compound
Rendimiento 34.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(Oc1c(Cl)cc(CO)cc1OC)c1ccccc1
Reaction #65509
title compound
Rendimiento 64.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCc1cc(CBr)cc(Cl)c1OC(C(=O)OC)c1ccc2c(c1)OCO2
Reaction #276887
DOI: 10.1039/C8SC04228D
O=C(CCc1ccc(OC(C(=O)O)c2ccccc2)c(Cl)c1Cl)c1ccc(-c2ccc(C(F)(F)F)cc2)s1
Reaction #288490
DOI: 10.1039/C8SC04228D
CCCCc1nc2ccc(NC(=O)NC3CCCCC3)cc2n1Cc1cc(Cl)c(OC(C(=O)O)c2ccccc2)c(Cl)c1
Reaction #295751
DOI: 10.1039/C8SC04228D
COC(=O)C(Oc1ccc(C)cc1Cl)c1ccccc1
Reaction #345005
title compound
Rendimiento 83.1%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(Oc1ccc(CBr)cc1Cl)c1ccccc1
Reaction #345006
title compound
Rendimiento 34.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCc1nc2ccc(C)cc2c(=O)n1Cc1ccc(OC(C(=O)OC)c2ccccc2)c(Cl)c1
Reaction #345007
title compound
Rendimiento 52.4%DOI: 10.6084/m9.figshare.5104873.v1
CCCCc1nc2ccc(C)cc2c(=O)n1Cc1ccc(OC(C(=O)O)c2ccccc2)c(Cl)c1
Reaction #345008
title compound
Rendimiento 71.4%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(Oc1c(Cl)cc(CO)cc1OC)c1ccccc1
Reaction #345011
title compound
Rendimiento 64.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCc1cc(CO)cc(Cl)c1OC(C(=O)OC)c1ccc2c(c1)OCO2
Reaction #362114
title compound
Rendimiento 81.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCc1cc(CBr)cc(Cl)c1OC(C(=O)OC)c1ccc2c(c1)OCO2
Reaction #362115
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCc1cc(Cn2c(=O)n(C(=O)OCC)c3ccccc32)cc(Cl)c1OC(C(=O)OC)c1ccc2c(c1)OCO2
Reaction #362116
title compound
Rendimiento 45.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCc1cc(Cn2c(=O)[nH]c3ccccc32)cc(Cl)c1OC(C(=O)O)c1ccc2c(c1)OCO2
Reaction #362117
title compound
Rendimiento 51.2%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(Oc1c(Cl)cc(Cn2c(=O)n(C(=O)OCC)c3ccccc32)cc1Cl)c1ccc2c(c1)OCO2
Reaction #362118
title compound
Rendimiento 64.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C(Oc1c(Cl)cc(Cn2c(=O)[nH]c3ccccc32)cc1Cl)c1ccc2c(c1)OCO2
Reaction #362119
title compound
Rendimiento 90.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(CCc1ccc(OC(C(=O)O)c2ccccc2)c(Cl)c1Cl)c1ccc(-c2ccc(C(F)(F)F)cc2)s1
Reaction #503254
2-(2,3-Dichloro-4-(3-oxo-3-(5-(4-(trifluoromethyl)phenyl)thien-2-yl)propyl)-phenoxy)-2-phenylacetic acid
DOI: 10.6084/m9.figshare.5104873.v1
CCCCc1nc2ccc(NC(=O)NC3CCCCC3)cc2n1Cc1cc(Cl)c(OC(C(=O)O)c2ccccc2)c(Cl)c1
Reaction #527783
2-n-Butyl-1-[4-[(α-carboxy)benzyloxy]-3,5-dichloro-benzyl]-6-cyclohexylaminocarbonylamino-benzimidazole
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(Oc1c(Cl)cc(CBr)cc1Cl)c1ccccc1
Reaction #922418
DOI: 10.1039/C8SC04228D
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