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1343873

COC(=O)C(=O)C=C([O-])c1c(OC)cccc1OC.[Na+]
Reaction #1177
expected product
DOI: 10.6084/m9.figshare.5104873.v1
N[C@H](Cc1ccccc1)C(=O)O
Reaction #2053
D-phenylalanine
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(=O)[O-].[K+]
Reaction #4059
Potassium ethyl oxalate
Ausbeute 79.2%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-])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-])C(=O)[O-].O=C([O-])C(=O)[O-].O=C([O-])C(=O)[O-].[Ce+3].[Ce+3]
Reaction #10211
cerium oxalate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1coc(N)n1
Reaction #42612
ethyl 2-amino-1,3-oxazole-4-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
O=C1C=C/C(=C(/c2ccc(O)c(O)c2)c2ccccc2S(=O)(=O)O)C=C1O.[Mo]
Reaction #47726
Pyrocatechol Violet Molybdenum
DOI: 10.6084/m9.figshare.5104873.v1
COc1ncc(OC)c2c(C(=O)C(=O)[O-])c[nH]c12.[K+]
Reaction #48485
Potassium (4,7-dimethoxy-6-azaindol-3-yl)-oxoacetate
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CN(C(=O)c2ccccc2)CCN1C(=O)C(=O)c1c[nH]c2ncccc12
Reaction #48486
(R)-N-(benzoyl)-3-methyl-N′-[(7-azaindol-3-yl)-oxoacetyl]-piperazine
DOI: 10.6084/m9.figshare.5104873.v1
O=C([O-])C(=O)c1c[nH]c2ncccc12.[K+]
Reaction #48487
Potassium (7-azaindol-3-yl)-oxoacetate
DOI: 10.6084/m9.figshare.5104873.v1
O=C1CSC(C(=O)O)O1
Reaction #52556
5-oxo-1,3-oxathiolane-2-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C(=O)c1ccc(C2CCCCC2)c([N+](=O)[O-])c1
Reaction #54838
3-nitro-4-cyclohexylphenylglyoxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
NC(C(=O)O)c1ccc(O)cc1
Reaction #75218
DL-p-hydroxyphenylglycine
Ausbeute 50.4%DOI: 10.6084/m9.figshare.5104873.v1
NC(C(=O)O)c1ccc(O)cc1
Reaction #75219
DL-p-hydroxyphenylglycine
Ausbeute 33.6%DOI: 10.6084/m9.figshare.5104873.v1
NC(C(=O)O)c1ccc(O)cc1
Reaction #75221
DL-p-hydroxyphenylglycine
Ausbeute 40.5%DOI: 10.6084/m9.figshare.5104873.v1
NC(C(=O)O)c1ccc(O)cc1
Reaction #75222
DL-p-hydroxyphenylglycine
Ausbeute 34.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CNc1ccc(O)c(O)c1
Reaction #75223
(3,4-dihydroxyphenyl)glycine
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CNc1ccc(O)c(O)c1O
Reaction #75224
(2,3,4-trihydroxyphenyl)glycine
Ausbeute 20.6%DOI: 10.6084/m9.figshare.5104873.v1
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