silver

[Ag]
Reaction #43395
silver
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=C(O)CC(O)(CC(=O)O)C(=O)[O-].[Ag+]
Reaction #43396
silver dihydrogen citrate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=CCc1ccccc1
Reaction #56123
phenylacetaldehyde
Ausbeute 67.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09
ON=C(CCN1CCCCC1)c1ccccc1
Reaction #63290
subject compound
Ausbeute 74.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
COCc1ccsc1-c1nsc2ccc(-n3c(=O)cc(C(F)(F)F)n(C)c3=O)cc12
Reaction #77247
title compound
Ausbeute 87.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
C[C@@H]1O[C@@H](OC[C@H]2O[C@@H](Oc3c(-c4ccc(O)cc4)oc4cc(O[C@@H]5O[C@@H](C)[C@H](O)[C@@H](O)[C@H]5O)cc(O)c4c3=O)[C@H](O)[C@@H](O)[C@H]2O)[C@H](O)[C@H](O)[C@H]1O.[Ag]
Reaction #89802
Robinin silver
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
COc1ccc([C@@H]2CC(=O)c3c(O)cc(O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](C)[C@H](O)[C@@H](O)[C@H]5O)[C@@H](O)[C@H](O)[C@H]4O)cc3O2)cc1O.[Ag]
Reaction #89803
Hesperidin silver
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CC1OC(Oc2c(-c3cc(O)c(O)c(O)c3)oc3cc(O)cc(O)c3c2=O)C(O)C(O)C1O.[Ag]
Reaction #89805
Myricetin 3-rhamnoside silver
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
COC(=O)c1ccc(Cc2c[nH]c3ccc([N+](=O)[O-])cc23)c(OC)c1
Reaction #195528
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1cc(OC)nc(Oc2cccc(N)c2-c2cnco2)n1
Reaction #198680
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
[Ag]
Reaction #203691
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
C=CCOC(=O)OC(C)C1C(=O)N(C(C(=O)OCC=C)=P(c2ccccc2)(c2ccccc2)c2ccccc2)C1SC(=O)CCCCn1cnnn1
Reaction #211549
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=P([O-])([O-])[O-].O=P([O-])([O-])[O-].O=P([O-])([O-])[O-].[Ca+2].[Ca+2].[Ca+2].[Ca+2].[Ca+2].[OH-]
Reaction #216540
hydroxylapatite
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_11
CCCOC(C)Cc1ccc(-c2ccc(C(C)=O)cc2)cc1
Reaction #222531
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCOC(=O)c1cn(-c2nccs2)c2nc(N3CC(NC)C(OC)C3)ccc2c1=O
Reaction #244515
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=CCc1ccccc1
Reaction #247941
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=C(OCCC(F)=C(F)F)C(F)(F)C(F)(F)C(F)(F)F
Reaction #260087
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
C=CCOC(=O)OC(C)C1C(=O)N(C(C(=O)OCC=C)=P(c2ccccc2)(c2ccccc2)c2ccccc2)C1SC(=O)c1ccncc1
Reaction #272396
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
O=C([O-])c1cccc(C(=O)[O-])c1.[Ag+2]
Reaction #319170
silver isophthalate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1989_07
O=C1CCN(c2ccccc2)N1.Oc1ccc(O)cc1
Reaction #343031
hydroquinone phenidone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1987_10
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