An 55 Reaktionen beteiligt

15556

COC(=O)c1ccc(OC)c(Cl)c1
Reaction #7520
title compound
Ausbeute 100.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=C(Nc1ccccc1)c1ccc(Cl)c(O)c1
Reaction #7858
4-chloro-3-hydroxy-N-phenylbenzamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COCOc1ccc(C(=O)O)cc1Cl
Reaction #49534
3-chloro-4-methoxymethoxybenzoic acid
Ausbeute 95.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(=O)Oc1ccc(C(=O)O)cc1Cl
Reaction #54995
4-Acetoxy-3-chlorobenzoic acid
Ausbeute 52.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_04
Nc1ccc(OCc2ccccc2)c(Cl)c1
Reaction #82701
4-benzyloxy-3-chloroaniline
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
COC(=O)c1ccc(O)c(Cl)c1
Reaction #160114
methyl 3-chloro-4-hydroxy-benzoate
Ausbeute 83.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
COC(=O)c1ccc(O)c(Cl)c1
Reaction #176984
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
C#CCOC(=O)c1ccc(O)c(Cl)c1
Reaction #184441
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(O)c1cc(Cl)c(O)c([N+](=O)[O-])c1
Reaction #198382
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(O)c1cc(Cl)c(O)c(S(=O)(=O)Cl)c1
Reaction #268663
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CC(=O)Oc1ccc(C(=O)O)cc1Cl
Reaction #311658
3-chloro-4-acetoxybenzoic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_11
CC(=O)Oc1ccc(C(=O)O)cc1Cl
Reaction #394498
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
—
Reaction #510539
white solid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_01
C#CCOC(=O)c1ccc(O)c(Cl)c1
Reaction #516575
Propargyl 3-Chloro-4-Hydroxybenzoate
Ausbeute 64.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_11
O=C(c1ccc(O)c(Cl)c1)N1CCC[C@@H]2c3ccccc3CC[C@@H]21
Reaction #542618
title compound
Ausbeute 42.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_07
O=C(c1ccc(O)c(Cl)c1)N1CCC[C@@H]2c3ccccc3C[C@@H]21
Reaction #542678
title compound
Ausbeute 32.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_07
O=C(c1ccc(O)c(Cl)c1)N1CCC[C@@H]2c3ccccc3CC[C@@H]21
Reaction #608277
title compound
Ausbeute 42.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_05
O=C(c1ccc(O)c(Cl)c1)N1CCC[C@@H]2c3ccccc3C[C@@H]21
Reaction #608337
title compound
Ausbeute 32.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_05
CCCCCCCCC(=O)Oc1ccc(C(=O)O)cc1Cl
Reaction #655508
3-chloro-4-octylcarbonyloxybenzoic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_03
O=C(O)C1=Cc2cc(Cl)c(Oc3ccc(C(=O)O)cc3Cl)cc2OC1C(F)(F)F
Reaction #737378
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_08
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