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2712

Cc1c(NN)ccc(C(=O)O)c1C.Cl
Reaction #1179
expected product
Ausbeute 93.7%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(O)cccc1C(=O)O
Reaction #8936
yellow solid
Ausbeute 36.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(N)c(C)c(C(=O)O)c1
Reaction #94664
3-amino- 2,5-dimethylbenzoic acid
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(N)c(C)c1Cl
Reaction #166188
title compound
Ausbeute 96.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(Br)cccc1C(=O)O
Reaction #188530
DOI: 10.1039/C8SC04228D
Cc1c(O)cccc1C(=O)O
Reaction #191868
DOI: 10.1039/C8SC04228D
Cl
Reaction #206841
DOI: 10.1039/C8SC04228D
Cc1c(N)cccc1C(=O)O
Reaction #229362
DOI: 10.1039/C8SC04228D
Cc1c(O)cccc1C(=O)O
Reaction #238172
DOI: 10.1039/C8SC04228D
COC(=O)c1cccc(N)c1C
Reaction #253829
DOI: 10.1039/C8SC04228D
Cc1c(NS(=O)(=O)c2ccc(Br)cc2)cccc1C(=O)O
Reaction #263746
DOI: 10.1039/C8SC04228D
Cc1c(NS(=O)(=O)c2ccc(Br)cc2)cccc1C(=O)O
Reaction #308596
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(N)cccc1C(=O)O
Reaction #335852
3-amino-2-methylbenzoic acid
Ausbeute 105.5%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(N)c(C)c(C(=O)O)c1
Reaction #346756
3-amino-2,5-dimethylbenzoic acid
DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(O)cccc1C(=O)O
Reaction #347568
desired subtitled compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(C(=O)O)c1C
Reaction #347985
material
DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(N)cccc1C(=O)O
Reaction #347986
3-amino-2-methylbenzoic acid
DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(C(=O)O)c1C
Reaction #347987
3-methoxy-2-methylbenzoic acid
DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(O)cccc1C(=O)O
Reaction #378756
DOI: 10.1039/C8SC04228D
COC(=O)c1ccc(N)c([N+](=O)[O-])c1C
Reaction #385270
DOI: 10.1039/C8SC04228D
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