An 135 Reaktionen beteiligt

14882

COc1ccc(C(=O)c2ccccc2F)cc1
Reaction #10213
(2-fluoro-phenyl)-(4-methoxy-phenyl)-methanone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
C#CC(Nc1cccc2ccccc12)c1ccccc1
Reaction #42707
title compound
Ausbeute 83.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
c1cc(Nc2cccc3ccccc23)cc(C2OCCO2)c1
Reaction #70673
N-(3-(1,3-dioxolan-2-yl)phenyl)naphthalen-1-amine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
Clc1nc2ccccc2nc1Nc1cccc2ccccc12
Reaction #72484
Compound 2c
Ausbeute 33.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
O=C(CC1CCc2cc(Br)cc3[nH]c(=O)c(=O)n1c23)Nc1cccc2ccccc12
Reaction #80832
title compound
Ausbeute 73.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
Nc1c(Br)ccc2ccccc12
Reaction #167687
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
COc1cc2ncnc(Nc3cccc4ccccc34)c2cc1OC
Reaction #175891
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Nc1cccc2ccccc12
Reaction #200554
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCCN
Reaction #202322
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=O)CNc1cccc2ccccc12
Reaction #204750
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Clc1nc2ccccc2nc1Nc1cccc2ccccc12
Reaction #227810
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(C)(C)OC(=O)NCCCCC(NC(=O)OCc1cccc2c1Cc1ccccc1-2)C(=O)Nc1cccc2ccccc12
Reaction #244527
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cl
Reaction #250279
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCOC(CC)=Nc1cccc2ccccc12
Reaction #253264
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Nc1cccc2ccccc12
Reaction #258154
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COC(=O)C=Cc1cccc(S(=O)(=O)Nc2cccc3ccccc23)c1
Reaction #261133
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCc1cccc(NC(=N)Nc2cccc3ccccc23)c1
Reaction #290209
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COC(=O)C=Cc1cccc(S(=O)(=O)Nc2cccc3ccccc23)c1
Reaction #313331
title compound
Ausbeute 51.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
NS(=O)(=O)c1ccc(Cl)c([N+](=O)[O-])c1-c1cccc2ccccc12
Reaction #317724
naphthalen-1-yl-3-nitro-4-chloro-benzenesulphonamide
Ausbeute 78.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
c1ccc(C2(c3ccc(Nc4cccc5ccccc45)cc3)c3ccccc3-c3ccccc32)cc1
Reaction #326393
white solid
Ausbeute 52.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
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