An 39 Reaktionen beteiligt

1254617

O=C(c1ccc[nH]1)c1cccn1N1C(=O)c2ccccc2C1=O
Reaction #50672
product
Ausbeute 69.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
O=C(c1cccs1)c1cccn1N1C(=O)c2ccccc2C1=O
Reaction #50674
2-[2-(2-Thienylcarbonyl)-1H-pyrrol-1-yl]-1H-isoindole-1,3(2H) dione
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
Cc1ccsc1C(=O)c1cccn1N1C(=O)c2ccccc2C1=O
Reaction #50677
product
Ausbeute 25.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
CC(=O)c1cccn1N1C(=O)c2ccccc2C1=O
Reaction #50679
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
CC(C)C(=O)c1cccn1N1C(=O)c2ccccc2C1=O
Reaction #50683
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
CC(C)C(=O)c1cccn1N1C(=O)c2ccccc2C1=O
Reaction #276111
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
O=C(c1ccc[nH]1)c1cccn1N1C(=O)c2ccccc2C1=O
Reaction #283162
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
O=C(c1ccccc1F)c1cccn1N1C(=O)c2ccccc2C1=O
Reaction #367296
solid
Ausbeute 19.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1986_05
O=C(c1ccccc1Cl)c1cccn1N1C(=O)c2ccccc2C1=O
Reaction #367300
oil
Ausbeute 123.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1986_05
O=C(c1ccc[nH]1)c1cccn1N1C(=O)c2ccccc2C1=O
Reaction #415014
product
Ausbeute 69.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_12
O=C(c1cccs1)c1cccn1N1C(=O)c2ccccc2C1=O
Reaction #415016
2-[2-(2-Thienylcarbonyl)-1H-pyrrol-1-yl]-1H-isoindole-1,3(2H) dione
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_12
Cc1ccsc1C(=O)c1cccn1N1C(=O)c2ccccc2C1=O
Reaction #415019
product
Ausbeute 25.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_12
CC(=O)c1cccn1N1C(=O)c2ccccc2C1=O
Reaction #415021
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_12
CC(C)C(=O)c1cccn1N1C(=O)c2ccccc2C1=O
Reaction #415024
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_12
O=C(c1ccccc1F)c1cccn1N1C(=O)c2ccccc2C1=O
Reaction #549920
solid
Ausbeute 19.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1985_05
O=C(c1ccccc1Cl)c1cccn1N1C(=O)c2ccccc2C1=O
Reaction #549924
oil
Ausbeute 123.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1985_05
CC(=O)c1cccn1N1C(=O)c2ccccc2C1=O
Reaction #750148
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
O=C(c1ccccc1F)c1cccn1N1C(=O)c2ccccc2C1=O
Reaction #756152
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
O=C(c1cccs1)c1cccn1N1C(=O)c2ccccc2C1=O
Reaction #896940
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
O=C(c1cccn1N1C(=O)c2ccccc2C1=O)C1CC1
Reaction #1063412
N-(2-cyclopropanecarbonyl-1H-pyrrol-1-yl)phthalimide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_03
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