4-cyanobenzaldehyde

CCCCCC1COC(c2ccc(C#N)cc2)OC1C
Reaction #4585
2-p-cyanophenyl-5-n-pentyl-4-methyl-1,3-dioxane
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
COC=Cc1ccc(C#N)cc1
Reaction #4970
4-(2-methoxyvinyl)benzonitrile
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
N#Cc1ccc(CNC2CCCc3cccnc32)cc1
Reaction #7237
N-(5,6,7,8-tetrahydro-8-quinolinyl)-4-cyanobenzylamine
수율 72.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC1=NC(=Cc2ccc(C#N)cc2)C(=O)O1
Reaction #7296
4-(2-Methyl-5-oxooxazol-4-ylidenemethyl)benzonitrile
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COc1ccc(-c2cc3cc(F)c(F)cc3[nH]2)cc1NCc1ccc(C#N)cc1
Reaction #53809
product
수율 38.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
NCc1ccc(CO)cc1
Reaction #60597
4-hydroxymethylbenzylamine
수율 46.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CC(=O)C=Cc1ccc(C#N)cc1
Reaction #66947
crystals
수율 49.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
N#Cc1ccc(C(O)Cc2ccc(C#N)cc2[N+](=O)[O-])cc1
Reaction #75512
2-(4-cyano-2-nitro-phenyl)-1-(4-cyano-phenyl)-ethanol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
CC(C)(C)c1cc(C(c2ccc(C#N)cc2)N2CCCCC2)cc(C(C)(C)C)c1O
Reaction #81032
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
N#Cc1ccc(/C=C/c2nc3ccccc3c(=O)n2-c2cccc(-n3nn[nH]c3=O)c2)cc1
Reaction #87327
desired product
수율 70.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CC(C)(C)OC(=O)C1CN(Cc2ccc(C#N)cc2)C1
Reaction #158403
tert-butyl 1-(4-cyanobenzyl)azetidine-3-carboxylate
수율 89.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
N#Cc1ccc(CN2CC(C(=O)O)C2)cc1
Reaction #158404
1-(4-cyanobenzyl)azetidine-3-carboxylic acid
수율 75.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
N#Cc1ccc(CN[C@H]2CC[C@@H](C(c3ccccc3)c3ccccc3)OC2)cc1
Reaction #166084
compound 16c
수율 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
COc1cc(-c2cnc3c(c2)C(=Cc2ccc(C#N)cc2)C(=O)N3)cc(OC)c1OC
Reaction #172227
title compound
수율 54.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
N#Cc1ccc(CNc2ccc(C(=O)N3CCN(c4ccccc4)CC3)cc2)cc1
Reaction #175755
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
N#Cc1ccc(C2OCc3ccccc3S2)cc1
Reaction #177524
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
N#Cc1ccc(CN2CCC(N3C(=O)Nc4ccccc4C3c3ccccc3)CC2)cc1
Reaction #187382
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(=O)C=Cc1ccc(C#N)cc1
Reaction #199690
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
N#Cc1ccc(CN2CC(C(=O)O)C2)cc1
Reaction #202235
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)(C)OC(=O)C=Cc1ccc(C#N)cc1
Reaction #208284
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
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