Citrate

CC(C)=O.CO.O=C([O-])CC(O)(CC(=O)[O-])C(=O)[O-]
Reaction #857
Citrate Acetone MeOH
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)=O.CO.O=C([O-])CC(O)(CC(=O)[O-])C(=O)[O-]
Reaction #858
Citrate Acetone MeOH
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C([O-])CC(O)(CC(=O)[O-])C(=O)[O-].[Cu+2].[Li+].[Li+]
Reaction #94101
Dilithium monocopper(II) citrate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1978_12
CC(=O)NC1(c2ccccc2)CCN(CCC(c2ccc(Cl)c(Cl)c2)C(OC(C)=O)c2ccnn2-c2ccccc2)CC1
Reaction #178137
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(O)CC(O)(CC(=O)O)C(=O)O
Reaction #190192
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CN(CC(CCN1CCC(c2ccccc2S(C)(=O)=O)CC1)c1ccc(F)c(F)c1)C(=O)c1cccc2c1CCCC2
Reaction #205201
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(O)CC(O)(CC(=O)O)C(=O)O
Reaction #235953
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=C(O)CC(O)(CC(=O)O)C(=O)O
Reaction #237283
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
OCC1OC(n2cnc3cc(Cl)c(Cl)cc32)C(F)C1O
Reaction #239828
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCCCC(C)C(O)C=CC1CCC2(OCCO2)C1CCCCCCCO
Reaction #241416
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=C([O-])CC(O)(CC(=O)[O-])C(=O)[O-]
Reaction #276418
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCOC(=O)c1ccnc(C(=O)NC)c1
Reaction #283438
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
NC(=O)c1cc(COc2nnc(Nc3ccc(Cl)cc3)c3ccsc23)ccn1
Reaction #286662
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CN(C)c1nc(N)nc2c1ncn2C1CC(N=[N+]=[N-])C(CO)O1
Reaction #386079
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
O=C(O)CC(O)(CC(=O)O)C(=O)O
Reaction #389697
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CC(=O)Nc1ccccc1C1CCN(CCC(CN(C)C(=O)c2cc(C#N)cc3ccccc23)c2ccc(Cl)c(Cl)c2)CC1
Reaction #391148
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
O=C(O)CC(O)(CC(=O)O)C(=O)O
Reaction #400863
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CC1=CC(=O)c2c(O)cccc2C1=O
Reaction #422227
Plumbagin
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
COc1ccc(CN(CCN(C)C)c2ccccn2)cc1.O=C(O)/C=C\C(=O)O
Reaction #431836
Pyrilamine maleate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1991_10
OC[C@H]1O[C@@H](n2cnc3cc(Cl)c(Cl)cc32)[C@H](F)[C@@H]1O
Reaction #444172
compound 15
Ausbeute 67.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_11
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