Busqueda de Subestructura

CCC(C)(C)O

OC1(C2CC2)CCc2cc(F)ccc21
Reaction #41969
title compound
Rendimiento 106.8%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCC(C)(C)c1ccc(C2(O)CCCN(Cc3ccccc3)C2)c(OCc2ccccc2)c1
Reaction #54339
title compound
Rendimiento 67.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCC(C)(C)c1ccc(C2(O)CCCNC2)c(O)c1
Reaction #54340
title compound
Rendimiento 70.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NC1CCN(CC(c2ccc(Cl)c(Cl)c2)C2(O)CCCCC2)CC1
Reaction #57084
tert-butyl {1-[2-(3,4-dichlorophenyl)-2-(1-hydroxycyclohexyl)ethyl]piperidin-4-yl}carbamate
Rendimiento 53.0%DOI: 10.6084/m9.figshare.5104873.v1
Cl.Cl.N[C@@H]1CCN(CC(c2ccc3ccccc3c2)C2(O)CCCCC2)C1
Reaction #57119
1-[2-[(3R)-3-aminopyrrolidin-1-yl]-1-(2-naphthyl)ethyl]cyclohexanol Dihydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
CN[C@@H]1CCN(CC(c2ccc3ccccc3c2)C2CCCCC2O)C1.Cl.Cl
Reaction #57120
2-[(3R)-3-(methylamino)pyrrolidin-1-yl-1-(2-naphthyl]ethyl}cyclohexanol Dihydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(CC(c2ccc(OCc3ccc(C(F)(F)F)cc3)c(F)c2)C2(O)CCCCC2)CC1.Cl.Cl
Reaction #57124
1-[1-(3-fluoro-4-{[4-(trifluoromethyl)benzyl]oxy}phenyl)-2-(4-methylpiperazin-1-yl)ethyl]cyclohexanol Dihydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
COCC(=O)C(O)(CC(=O)[O-])C[N+](C)(C)C.[Cl-]
Reaction #63654
methoxy acetyl carnitine chloride
Rendimiento 75.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOCC(=O)C(O)(CC(=O)[O-])C[N+](C)(C)C.[Cl-]
Reaction #63655
title compound
Rendimiento 75.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCc1nc(C(O)(CC)CC)c(C(=O)OCC)n1Cc1ccc(-c2ccccc2-c2nnnn2C(c2ccccc2)(c2ccccc2)c2ccccc2)cc1
Reaction #81172
title compound
Rendimiento 52.1%DOI: 10.6084/m9.figshare.5104873.v1
CCCCc1nc(C(C)(O)CC)c(C#N)n1Cc1ccc(-c2ccccc2-c2nnnn2C(c2ccccc2)(c2ccccc2)c2ccccc2)cc1
Reaction #81175
title compound
Rendimiento 72.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCc1nc(C(C)(O)CC)c(C#N)n1Cc1ccc(-c2ccccc2-c2nnnn2C(c2ccccc2)(c2ccccc2)c2ccccc2)cc1
Reaction #81178
title compound
Rendimiento 77.4%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(C#CCCCC(C)(O)c2ccc(Cl)c(Cl)c2)ccc1-n1cnc(C)n1
Reaction #158337
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-c2nnn3c2CCCC3(C)c2ccc(Cl)c(Cl)c2)ccc1-n1cnc(C)n1
Reaction #158338
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(C)(C)C(NC(=O)OC(C)(C)C)C(=O)O
Reaction #159228
2-tert-Butoxycarbonylamino-3-methoxy-3-methyl-butyric acid
Rendimiento 94.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(C)(C)C(NC(=O)OC(C)(C)C)C(=O)O
Reaction #167170
2-tert-Butoxycarbonylamino-3-methoxy-3-methyl-butyric acid
Rendimiento 94.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCOc1ccc(CN2CCC(C(O)(c3ccc(Cl)cc3)c3ccc(OC(F)(F)F)cc3)CC2)cc1
Reaction #174959
DOI: 10.1039/C8SC04228D
COC(=O)c1cccc(C(=O)NC(CC(=O)N2CCC(O)(c3ccc(Cl)cc3)C(C)(C)C2)C(C)C)c1
Reaction #177093
DOI: 10.1039/C8SC04228D
CN(CCCc1nc2c(Cl)cccc2[nH]1)CCC1(O)CC2CCC1C=C2c1ccccc1
Reaction #177377
DOI: 10.1039/C8SC04228D
COc1cccc(CC2CCCC=C2c2nc(-c3ccccc3)c(-c3ccccc3)o2)c1
Reaction #180473
DOI: 10.1039/C8SC04228D
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