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10645

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
NCc1ccccc1-c1ccc(C(=O)Nc2ccccc2C(=O)Nc2ccc(Cl)cn2)cc1
Reaction #40412
{4-[2-(aminomethyl)phenyl]phenyl)-N-(2-[N-(5-chloro(2-pyridyl))carbamoyl]phenyl}carboxamide
Ausbeute 43.1%DOI: 10.6084/m9.figshare.5104873.v1
NCc1ccc(C(=O)Nc2ccccc2C(=O)Nc2ccc(Cl)cn2)cc1
Reaction #40413
[4-(aminomethyl)phenyl]-N-{2-[N-(5-chloro(2-pyridyl))carbamoyl]phenyl}carboxamide
Ausbeute 32.3%DOI: 10.6084/m9.figshare.5104873.v1
NCc1ccccc1-c1ccc(C(=O)Nc2ccccc2C(=O)Nc2ccc(Cl)cn2)cc1
Reaction #40441
{4-[2-(aminomethyl)phenyl]phenyl}-N-{2-[N-(5-chloro(2-pyridyl))carbamoyl]phenyl}carboxamide
Ausbeute 43.1%DOI: 10.6084/m9.figshare.5104873.v1
NCc1ccc(C(=O)Nc2ccccc2C(=O)Nc2ccc(Cl)cn2)cc1
Reaction #40442
[4-(aminomethyl)phenyl]-N-{2-[N-(5-chloro(2-pyridyl))carbamoyl]phenyl}carboxamide
Ausbeute 32.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N[C@@H](CS)C(=O)O.[Cl][Co][Cl]
Reaction #167465
cobalt-dichloride-N-acetyl cysteine
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #170080
crude product
DOI: 10.6084/m9.figshare.5104873.v1
O=C1NC(=O)C(Cc2ccc(OCC(O)c3ccccc3)cc2)S1
Reaction #180621
DOI: 10.1039/C8SC04228D
O=C1OCc2ncccc21
Reaction #189410
DOI: 10.1039/C8SC04228D
O=C1NC(=O)C(Cc2ccc(OCC(O)c3ccccc3F)cc2)S1
Reaction #203549
DOI: 10.1039/C8SC04228D
COC(=O)CCC(CCCCCl)c1cccc(-c2cccnc2)c1
Reaction #204724
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)COc1cccc(CCN)c1
Reaction #205406
DOI: 10.1039/C8SC04228D
CSCC[C@H](N)C(=O)O
Reaction #215180
L-methionine
DOI: 10.6084/m9.figshare.5104873.v1
CSCC[C@H](N)C(=O)O
Reaction #215181
L-methionine
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)C1CC1F
Reaction #217794
title compound
Ausbeute 98.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CC1F
Reaction #217795
title compound
Ausbeute 96.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)C1CC1F
Reaction #217796
title compound
Ausbeute 84.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)C1CC1
Reaction #217797
title compound
Ausbeute 80.0%DOI: 10.6084/m9.figshare.5104873.v1
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