Participa en 171 reacciones

12755

N#Cc1ccc(F)cc1
Reaction #10020
4-fluorobenzo-nitrile
Rendimiento 75.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
N#Cc1ccc(-c2ccccc2)cc1
Reaction #42153
4-cyanobiphenyl
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
N#Cc1ccc(-c2ccccc2)cc1
Reaction #42171
4-cyanobiphenyl
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
N#Cc1ccc(Cl)cc1
Reaction #65060
4-Chlorobenzonitrile
Rendimiento 75.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
N#CC=C(N)c1ccc(Cl)cc1
Reaction #74835
β-amino-4-chlorocinnamonitrile
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_11
CS(=O)(=O)c1ccc(NC(=N)c2ccc(Cl)cc2)cc1
Reaction #80572
4-chloro-N-[4-(methylsulfonyl)phenyl]benzenecarboximidamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
NC(=NO)c1ccc(Cl)cc1
Reaction #87536
desired product
Rendimiento 40.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
N#Cc1ccc([N+](=O)[O-])cc1
Reaction #166172
4-Nitrobenzonitrile
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
N#Cc1ccc(N2C(=O)Cc3ccccc32)cc1
Reaction #166174
4-(2-Oxoindolin-1-yl)benzonitrile
Rendimiento 71.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CSc1ccc(NC(=N)c2ccc(Cl)cc2)cc1
Reaction #174618
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
N#Cc1ccc(N(c2ccccc2)c2ccccc2)cc1
Reaction #187928
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCCCCCCCCCCSc1ccc(C#N)cc1
Reaction #191351
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
NC(=Cc1nccs1)c1ccc(Cl)cc1
Reaction #211025
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
N#CC=C(N)c1ccc(Cl)cc1
Reaction #212259
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
N#CC=C(N)c1ccc(Cl)cc1
Reaction #215346
β-amino-4-chlorocinnamonitrile
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1981_03
CCCCCCNc1ccc(C#N)cc1
Reaction #226115
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
N#Cc1ccc(N(c2ccccc2)c2ccccc2)cc1
Reaction #228675
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
N#Cc1ccc(-c2ccccc2)cc1
Reaction #229028
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COc1nn(C)c(=O)n1Cc1cc(-c2ccc(C#N)cc2)ccc1C
Reaction #286960
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
N#Cc1ccc(OCC(F)(F)C(F)F)cc1
Reaction #290013
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
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