bis(tri-t-butylphosphino)palladium

Cc1ccc(/C=C/c2cccc3c4c([nH]c23)C2CCN(CC2)C4)cn1
Reaction #66064
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
Cc1ccc(C#Cc2cccc3c4c([nH]c23)C2CCN(CC2)C4)cn1
Reaction #66066
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
C(=C\c1cccc2c3c([nH]c12)C1CCN(CC1)C3)/c1cccnc1
Reaction #66085
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
C(=Cc1cccc2c3c([nH]c12)C1CCN(CC1)C3)c1cccnc1
Reaction #302416
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CC(C)(C)OC(=O)N1CCC[C@H](Nc2ncnc3c(C(N)=O)cc(-c4ccccc4)cc23)C1
Reaction #561657
tert-butyl (3S)-3-{[8-(aminocarbonyl)-6-phenylquinazolin-4-yl]amino}piperidine-1-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_01
CC(C)(C)OC(=O)N1CCC[C@H](Nc2ncnc3c(C(N)=O)cc(-c4ccccc4)cc23)C1
Reaction #665896
tert-butyl (3S)-3-{[8-(aminocarbonyl)-6-phenylquinazolin-4-yl]amino}piperidine-1-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_05
CC(C)(C)CC(=O)Nc1nn2cccnc2c1C#Cc1ccc(OC(F)(F)F)cc1
Reaction #898484
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
C=Cc1cnn(-c2ccc(Cn3cc(C(=O)OCC)c(=O)c4c(F)cccc43)cc2)c1
Reaction #899511
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
N#Cc1ccc(C(F)(F)F)c(C(=O)OCc2ccccc2)c1
Reaction #976713
title compound
Ausbeute 57.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_08
Cc1ccc(C#Cc2cccc3c4c([nH]c23)C2CCN(CC2)C4)cn1
Reaction #1234240
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (7/10)
Cc1ccc(C=Cc2cccc3c4c([nH]c23)C2CCN(CC2)C4)cn1
Reaction #1312300
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (5/10)
C=CCn1c(=O)n(CC(C)(C)C)c2ccc(-c3cc(C(C)(C)O)ccc3C)nc21
Reaction #1703425
1-(2,2-dimethylpropyl)-5-[5-(1-hydroxy-1-methylethyl)-2-methylphenyl]-3-prop-2-en-1-yl-1,3-dihydro-2H-imidazo[4,5-b]pyridin-2-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_07
Cc1ccc(C#Cc2cccc3c4c([nH]c23)CC2CNC4C2)cn1
Reaction #1710241
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_07
CC(C)(C)CC(=O)Nc1nn2cccnc2c1C#Cc1ccc(OC(F)(F)F)cc1
Reaction #2000142
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_12
CCOC(=O)c1cn(Cc2ccc(-n3cc(C#N)cn3)cc2)c2cccc(F)c2c1=O
Reaction #2056622
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_04
C=Cc1cnn(-c2ccc(Cn3cc(C(=O)OCC)c(=O)c4c(F)cccc43)cc2)c1
Reaction #2056623
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_04
CCOC(=O)c1cn(Cc2ccc(-c3cn[nH]c3)cn2)c2c(F)ccc(F)c2c1=O
Reaction #2155100
ethyl 5,8-difluoro-4-oxo-1-{[5-(1H-pyrazol-4-yl)pyridin-2-yl]methyl}-1,4-dihydroquinoline-3-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_10
CCOC(=O)c1cn(Cc2ccc(-n3cc(C#N)cn3)cc2)c2cccc(F)c2c1=O
Reaction #2414544
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (10/10)
Cc1ccc(/C=C/c2cccc3c4c([nH]c23)CCN(C)C4)cn1
Reaction #2494368
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_08
Cc1ccc(C#Cc2cccc3c4c([nH]c23)CCN(C)C4)cn1
Reaction #2494369
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_08
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