2-cyanobenzaldehyde

N#Cc1ccccc1CNc1cc2c3c(c1)[C@@H]1CNCC[C@@H]1N3CCOC2
Reaction #51559
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
N#Cc1ccccc1CNc1cc2c3c(c1)[C@@H]1CNCC[C@@H]1N3CCSC2
Reaction #51569
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CC(C)(C)[Si](O)(c1ccccc1)c1ccccc1
Reaction #53626
TBDPSOH
المردود 141.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
N#Cc1ccccc1CNc1cc2c3c(c1)[C@@H]1CNCC[C@@H]1N3CCOC2
Reaction #75846
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
N#Cc1ccccc1CNc1cc2c3c(c1)[C@@H]1CNCC[C@@H]1N3CCSC2
Reaction #75858
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
CCOC(=O)/C=C/c1ccccc1C#N
Reaction #172113
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
COC(=O)C(=Cc1ccccc1C#N)C(=O)C(OC)OC
Reaction #181035
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
N#Cc1ccccc1C(=O)O
Reaction #190969
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
N#Cc1ccccc1C=NNc1cc(N2CCOCC2)n2nc(-c3ccccc3)cc2n1
Reaction #195588
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
N#Cc1ccccc1CN1CCN(c2ccc3nnc(C(F)(F)F)n3n2)CC1
Reaction #280053
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Cc1ccc2nc(-c3ccccc3C#N)c(NC3CCCCC3)n2c1
Reaction #311025
المردود 31.0%Imidazopyridines dataset
CCOC(=O)C1=C(N)NC2=C(C(=O)CCC2)C1c1ccccc1C#N
Reaction #355253
2-amino-4-(2-cyanophenyl)-1,4,5,6,7,8-hexahydro-5-oxoquinoline-3-carboxylic acid ethyl ester
المردود 49.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1976_03
COC(=O)c1ccccc1-c1nc2cc(C)ccc2o1
Reaction #360926
2-hydroxy-5-methyl-N-(2-cyanobenzylidene)aniline
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_02
C[Si](C)(C)CCOCn1ccc2cc(C(O)c3ccccc3C#N)ccc21
Reaction #408522
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
Cc1cccc(C=Cc2ccccc2C#N)n1
Reaction #518211
2-[2-(6-Methyl-pyridin-2-yl)-vinyl]-benzonitrile
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_12
N#CC1=C(C2CCNCC2)Nc2n[nH]cc2C1c1ccccc1C#N
Reaction #576648
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_12
CC(C)Cn1c(=O)n(C)c(=O)c2cc(C3OC(=N)c4ccccc43)sc21
Reaction #655099
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_01
N#Cc1ccccc1/C=C/C=O
Reaction #708771
2-cyano-(E)-cinnamaldehyde
المردود 45.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1989_04
CC(C)Cn1c(=O)n(C)c(=O)c2cc(C3OC(=N)c4ccccc43)sc21
Reaction #758661
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
CCOC(=O)/C=C/c1ccccc1C#N
Reaction #803174
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_11
الصفحة 1التالي