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948383

CCOc1c(C(=O)O)c(C(=O)O)c(OCC)c2ccccc12
Reaction #43992
1,4-diethoxy-2,3-naphthalenedicarboxylic acid
Ausbeute 92.3%DOI: 10.6084/m9.figshare.5104873.v1
CCOc1c2c(c(OCC)c3ccccc13)C(=O)OC2=O
Reaction #43993
1,4-diethoxy-2,3-naphthalenedicarboxylic anhydride
Ausbeute 99.3%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)Cc1ccc(N2C(=O)c3c(c(OCC)c4ccccc4c3OCC)C2=O)cc1
Reaction #43994
ethyl[4-(4,9-diethoxy-1,3-dioxo-1,3-dihydro-2H-benzo[f]isoindol-2-yl)phenyl]acetate
DOI: 10.6084/m9.figshare.5104873.v1
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
COc1c2c(c(OC)c3ccccc13)C(=O)C1CC(O)(C(C)O)CCC1C2
Reaction #197544
DOI: 10.1039/C8SC04228D
CCOC(=O)Cc1ccc(N2C(=O)c3c(c(OCC)c4ccccc4c3OCC)C2O)cc1F
Reaction #203424
DOI: 10.1039/C8SC04228D
CCOC(=O)c1c(C)c(OC)c2ccccc2c1OC
Reaction #206119
DOI: 10.1039/C8SC04228D
CCOc1c2c(c(OC(F)F)c3ccccc13)CN(c1ccc(CC(=O)O)cc1Cl)C2=O
Reaction #208294
DOI: 10.1039/C8SC04228D
COc1c(C)c(C=O)c(OC)c2ccccc12
Reaction #208960
DOI: 10.1039/C8SC04228D
CCOC(=O)Cc1cc(F)c(N2C(=O)c3c(c(OCC)c4ccccc4c3OCC)C2O)c(F)c1
Reaction #244592
DOI: 10.1039/C8SC04228D
C=Cc1c(C(=O)OC)c2c(c3ccccc13)OC(c1ccccc1)(c1ccccc1)C=C2
Reaction #249794
DOI: 10.1039/C8SC04228D
CCOc1c2c(c(OCC(F)(F)F)c3ccccc13)C(=O)N(c1ccc(CC(=O)O)cc1Cl)C2
Reaction #251183
DOI: 10.1039/C8SC04228D
CCOC(=O)Cc1ccc(N2C(=O)c3c(c(OCc4ccccc4)c4ccccc4c3OCC)C2=O)c(F)c1
Reaction #260303
DOI: 10.1039/C8SC04228D
CCOC(=O)c1c(C(=O)OCC)c(OCc2ccccc2)c2ccccc2c1OCc1ccccc1
Reaction #309604
title compound
Ausbeute 109.4%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1c(C(=O)O)c(OCc2ccccc2)c2ccccc2c1OCc1ccccc1
Reaction #309605
title compound
Ausbeute 89.7%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)Cc1ccc(N2C(=O)c3c(c(OCc4ccccc4)c4ccccc4c3OCc3ccccc3)C2=O)cc1
Reaction #309608
title compound
Ausbeute 99.4%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)Cc1ccc(N2C(=O)c3c(c(O)c4ccccc4c3O)C2=O)c(Cl)c1
Reaction #309609
title compound
Ausbeute 9.8%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)Cc1ccc(N2Cc3c(c(OC(F)F)c4ccccc4c3OC(F)F)C2=O)c(F)c1
Reaction #309610
title compound
Ausbeute 45.8%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1c(C(=O)OCC)c(OCc2ccccc2)c2ccccc2c1OCC
Reaction #309612
title compound
Ausbeute 98.0%DOI: 10.6084/m9.figshare.5104873.v1
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