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CCOC(=O)c1ccccc1O

CCOC(=O)c1c(C)c(OC)c2ccccc2c1OC
Reaction #43996
ethyl 1,4-dimethoxy-2-methylnaphthalene-3-carboxylate
Ausbeute 89.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1c2c(c(OC)c3ccccc13)C(=O)N(c1ccc(CC(=O)O)cc1)C2
Reaction #43997
[4-(4,9-dimethoxy-1-oxo-1,3-dihydro-2H-benzo[f]isoindol-2-yl)phenyl]acetic acid
Ausbeute 15.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1c(OCC(F)(F)F)ccc([N+](=O)[O-])c1N
Reaction #46893
2-Amino-3-nitro-6-(2,2,2-trifluoro-ethoxy)-benzoic acid ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #49720
compound ( 1 )
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(Oc2cccc(-c3ccccc3)c2C(=O)OCc2ccccc2)nc(OC)n1
Reaction #49721
benzyl 2-(2,6-dimethoxypyrimidine-4-yloxy)-6-phenylbenzoate
Ausbeute 85.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1OC(=S)c2c(O)cccc21
Reaction #50455
7-hydroxy-3-methylisobenzofuran-1(3H)-thione
DOI: 10.6084/m9.figshare.5104873.v1
CC1OC(=S)c2c(O)cccc21
Reaction #50457
7-hydroxy-3-methyl-isobenzofuran-1(3H)-thione
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc(NC(=O)c2cc(Cl)ccc2OC)cc1OCC
Reaction #55745
2-ethoxy-4-(5-chloro-2-methoxy-benzamido)-benzoic acid ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc2c(c(/C=C/c3ccc(F)cc3)nn2C(=O)OC(C)(C)C)c1OCCOC1CCCCO1
Reaction #62326
title compound
Ausbeute 56.5%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc2c(c(/C=C/c3ccc(F)cc3)nn2C(=O)OC(C)(C)C)c1OCCO
Reaction #62327
title compound
Ausbeute 69.8%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccccc1OCc1ccccc1
Reaction #66917
73
Ausbeute 94.7%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1ccccc1OCc1ccccc1
Reaction #66918
78
Ausbeute 84.6%DOI: 10.6084/m9.figshare.5104873.v1
C=CCOC(=O)c1c(Oc2nc(OC)cc(OC)n2)ccc2oc(C)c(C(=O)O)c12
Reaction #80282
desired compound
Ausbeute 98.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CCOC(=O)c1c(Oc2nc(OC)cc(OC)n2)ccc2oc(C)c(C(=O)N(C)C)c12
Reaction #80283
desired compound
Ausbeute 60.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)nc(Oc2ccc3[nH]c(C)cc3c2C(=O)OCc2ccccc2)n1
Reaction #80288
desired product
Ausbeute 85.7%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)nc(Oc2ccc3[nH]c(C)c(C=O)c3c2C(=O)OCc2ccccc2)n1
Reaction #80289
desired compound
Ausbeute 81.5%DOI: 10.6084/m9.figshare.5104873.v1
C=CCOC(=O)c1c(Oc2nc(OC)cc(OC)n2)ccc2[nH]c(C)c([N+](=O)[O-])c12
Reaction #80290
desired compound
Ausbeute 55.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CCOC(=O)c1c(Oc2nc(OC)cc(OC)n2)ccc2[nH]c(C)c(NC(C)=O)c12
Reaction #80292
desired compound
Ausbeute 87.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1c(C)n(C(=O)c2ccccc2)c2ccc(Oc3nc(OC)cc(OC)n3)c(C(=O)OCc3ccccc3)c12
Reaction #80294
desired compound
Ausbeute 92.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1c(C)n(C(=O)c2ccccc2)c2ccc(Oc3nc(OC)cc(OC)n3)c(C(=O)O)c12
Reaction #80295
desired compound
Ausbeute 97.0%DOI: 10.6084/m9.figshare.5104873.v1
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