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O=C(O)c1ccc2cc(C(=O)O)ccc2c1
Reaction #2475
2,6-naphthalenedicarboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
O=C([O-])C(=O)[O-].[Co+2]
Reaction #6402
cobalt oxalate
DOI: 10.6084/m9.figshare.5104873.v1
O=C([O-])C(=O)[O-].O=C([O-])C(=O)[O-].O=C([O-])C(=O)[O-].[Ce+3].[Ce+3]
Reaction #6403
cerium oxalate
DOI: 10.6084/m9.figshare.5104873.v1
O=C([O-])[O-].O=C([O-])[O-].O=C([O-])[O-].[Nd+3].[Nd+3]
Reaction #6404
neodymium carbonate
DOI: 10.6084/m9.figshare.5104873.v1
O=C([O-])C(=O)[O-].O=C([O-])C(=O)[O-].O=C([O-])C(=O)[O-].[Sm+3].[Sm+3]
Reaction #6405
samarium oxalate
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1ccc(C(=O)O)cc1
Reaction #9836
terephthalic acid
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1ccc(C(=O)O)cc1
Reaction #9837
terephthalic acid
DOI: 10.6084/m9.figshare.5104873.v1
O=C1C=CC=C2C1=Cc1ccccc12
Reaction #9838
fluorenon
DOI: 10.6084/m9.figshare.5104873.v1
O=C1C=CC=C2C1=Cc1ccccc12
Reaction #9840
fluorenon
DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCCCC1
Reaction #9841
cyclohexanon
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Oc1ccc(C(=O)O)cc1
Reaction #9842
4-acetoxybenzoic acid
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Oc1cccc(C(=O)O)c1
Reaction #9843
3-acetoxybenzoic acid
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(C(=O)O)cc1
Reaction #9844
4-cyanobenzoic acid
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1ccc(C(=O)O)cc1
Reaction #9845
4-t-butylbenzoic acid
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1ccc(Cl)cc1
Reaction #9846
4-chlorobenzoic acid
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1ccccc1
Reaction #9847
benzoic acid
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1ccccc1[N+](=O)[O-]
Reaction #9848
2-nitrobenzoic acid
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1ccc([N+](=O)[O-])cc1
Reaction #9849
4-nitrobenzoic acid
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1ccc(C(=O)O)cc1
Reaction #9850
terephthalic acid
Ausbeute 95.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1ccc(C(=O)O)cc1
Reaction #9851
terephthalic acid
Ausbeute 97.0%DOI: 10.6084/m9.figshare.5104873.v1
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