3-hydroxybenzonitrile

CN(C)C(=S)Oc1cccc(C#N)c1
Reaction #6097
expected product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CC(=O)O[C@@H]1[C@@H](OC(C)=O)[C@H](OC(C)=O)CS[C@H]1Oc1cccc(C#N)c1
Reaction #6139
expected product
수율 33.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CC(=O)O[C@@H]1[C@@H](OC(C)=O)[C@H](OC(C)=O)CS[C@H]1Oc1cccc(C#N)c1
Reaction #6140
expected product
수율 25.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
N#Cc1cccc(Oc2ccccc2[N+](=O)[O-])c1
Reaction #40425
3-(2-nitrophenoxy)benzonitrile
수율 99.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
N#Cc1cccc(Oc2ccccc2[N+](=O)[O-])c1
Reaction #40453
3-(2-nitrophenoxy)benzonitrile
수율 99.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
N#Cc1cccc(Oc2cc3[nH]c(-c4ccccn4)nc3cc2Oc2ccccc2C#N)c1
Reaction #41515
5-(2-Cyano-phenoxy)-2-pyridin-2-yl-6-(3-cyano-phenoxy)-1H-benzimidazole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COC(=O)/C=C(\C)Oc1cccc(C#N)c1
Reaction #47430
(E)-3-(3-cyano-phenoxy)-but-2-enoic acid methyl ester
수율 76.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
NCc1cccc(OCC2CC2)c1
Reaction #69061
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
NC(=S)c1cccc(O)c1
Reaction #81853
3d
수율 57.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
N#Cc1cccc(OCn2ccc3ccc([N+](=O)[O-])cc32)c1
Reaction #84515
title compound
수율 51.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
N#Cc1cccc(OCC(N)=O)c1
Reaction #84561
title compound
수율 77.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
N#Cc1cccc(OCC(N)=O)c1
Reaction #84578
title compound
수율 28.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
N#CCOc1cccc(C#N)c1
Reaction #95047
3-cyanophenoxyacetonitrile
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_08
CCOC(=O)Cn1cc(-c2cccc(O)c2)nn1
Reaction #169494
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC1(C)COC(CCCOc2cccc(C#N)c2)(c2ccc(Br)cc2)OC1
Reaction #173794
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1c(F)c(F)nc(Oc2cccc(C#N)c2)c1F
Reaction #181481
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1ccc(Oc2cccc(C#N)c2)nc1
Reaction #182491
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)(C)OC(=O)NC(COc1cccc(C#N)c1)Cc1ccc(I)cc1
Reaction #194099
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC(=O)c1cc(COc2cccc(C#N)c2)cc(-c2cccc(C#N)c2)c1
Reaction #222268
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
N#Cc1cccc(Oc2cc3[nH]c(-c4ccccn4)nc3cc2Oc2ccccc2C#N)c1
Reaction #222381
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
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