ethanolate

CCOC(=O)/C(NC(C)=O)=C(/C)N(C)C
Reaction #162660
(E)-ethyl 2-acetamido-3-(dimethylamino)but-2-enoate
Ausbeute 50.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
COc1ccc(CCOc2ccc(NC(=O)N(C)OC)cc2)cc1
Reaction #173105
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1cccc(C(=NS(=O)C(C)(C)C)c2cc(Cl)cc(F)c2C#N)c1
Reaction #173304
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1ccc(C(C#N)C(=O)CN2CCCC2=O)cc1OC
Reaction #173771
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(O)c1cnc(N2CC3C(C2)C3N(CCN2CCCC2=O)S(=O)(=O)c2ccc3ccccc3c2)nc1
Reaction #174028
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=O)C(C(=O)OCC)C(=O)c1cc(F)c(F)c(Br)c1Cl
Reaction #176356
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1c(C(C)CC(O)(C=Nc2cccc3[nH]c(=O)ccc23)C(F)(F)F)ccc(Cl)c1F
Reaction #176431
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOc1c2ccccc2c(C=O)c2ccccc12
Reaction #176449
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOc1c(N2CCNCC2)c(F)cc2c(=O)c(C(=O)O)cn(C3CC3)c12
Reaction #177176
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCC(=O)C(C#N)c1ccc(OC)c(OC)c1
Reaction #177564
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOc1cccc2nc(-c3ccccc3Cl)c(NC3CCCCC3)n12
Reaction #178363
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=O)C(=O)CC(=O)CC(C)c1ccccc1
Reaction #178771
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=[N+]([O-])CC1(O)CN2CCC1CC2
Reaction #179189
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1cccc(C=Cc2nc3sccn3c(=O)c2-c2cccc(C(F)(F)F)c2)c1OCC1CC1
Reaction #179619
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCCCOc1c(C=Cc2nc3sccn3c(=O)c2-c2ccc(OC(F)(F)F)cc2)cccc1OC
Reaction #179818
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
N#CC=C1CCC2=C(C1)c1ccccc1Oc1ccccc12
Reaction #181030
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)(C)S(=O)N=C(C1CC1)C1CC1
Reaction #181558
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CSc1ccccc1OCCO
Reaction #182289
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC(=O)C(O)(c1ccc(C)cc1)c1ccc(C)cc1
Reaction #183159
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCOc1c(C=Cc2nc3sccn3c(=O)c2-c2ccc(C(F)(F)F)cc2)cccc1OC
Reaction #183312
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
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