An 21 Reaktionen beteiligt

956201

CCOC(=O)CNC(=O)OCc1ccco1

expected product

Ausbeute 66.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02

CCCCOC(=O)NS(=O)(=O)NCC(=O)OCC

Reaction #45244

ethyl 2-((N-(butyloxycarbonyl)sulfamoyl)amino)acetate

Ausbeute 85.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06

CCCCOC(=O)NS(=O)(=O)NCC(=O)OCC

Reaction #45252

ethyl 2-((N-(butyloxycarbonyl)sulfamoyl)amino)acetate

Ausbeute 85.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06

$CCOC(=O)CNC(=O)c1cccc(N/C(=C2\C(=O)Nc3ccccc32)c2ccccc2)c1$

Reaction #53031

(Z)-3-[1-(3-ethoxycarbonylmethylaminocarbonyl-phenylamino)-1-phenyl-methylidene]-2-indolinone

DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02

CCOC(=O)CNCC(O)COC

Reaction #53316

Ausbeute 100.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02

$CCCCCCCC/C=C\CCCCCCCC(=O)NCC(=O)O$

Reaction #53625

N-Oleoyl glycine

DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02

CCOC(=O)CNC1Cc2ccccc2C1

Reaction #173767

DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)

CCOC(=O)CNC(=O)CCc1ccc(O)cc1

Reaction #176699

DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)

CCOC(=O)CN=C(c1ccccc1)c1ccccc1

Reaction #178901

DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)

CCOC(=O)CNC(=O)Nc1ccc(F)cc1F

Reaction #185528

DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)

CCOC(=O)CNC(=O)c1ccc(NCCCCCCCCC2CCCCC2)cc1

Reaction #186548

DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)

CCOC(=O)CNC(=O)CC(C)(C)Nc1ccc(Cl)cc1

Reaction #190880

DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)

CCOC(=O)CNc1cc(C(=O)NC(CCC(=O)OC(C)(C)C)C(=O)N2CCN(C(=O)OCC)CC2)nc(-c2ccccc2)n1

Reaction #191238

DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)

CCOC(=O)CNC(=O)c1cn2nc(Cl)ccc2n1

Reaction #192248

DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)

CCOC(=O)CNC(=O)C(NC(=O)OCc1ccccc1)C(C)C

Reaction #193278

DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)

CCOC(=O)CNC(=O)c1ccc(S(=O)(=O)Nc2ccccc2C(=O)c2ccc(Cl)cc2Cl)cc1

Reaction #196407

DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)

CCOC(=O)CNC(=O)C(Cc1ccccc1)NC(=O)OC(C)(C)C

Reaction #199783

DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)

CCOC(=O)CNS(=O)(=O)c1ccccc1[N+](=O)[O-]

Reaction #199852

DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)

CCOC(=O)CNC1CCN(C(=O)OC(C)(C)C)CC1

Reaction #200266

DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)

CCOC(=O)CNC(=O)c1ccc(-c2ccccc2)cc1

Reaction #201962

DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)

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