Oxyma

CCOC(=O)C(N)C#N
Reaction #160783
titled compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCOC(=O)C(N)C#N
Reaction #218540
amino-cyano-acetic acid ethyl ester
Ausbeute 31.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
CCOC(=O)C(N)C#N
Reaction #218541
amino-cyano-acetic acid ethyl ester
Ausbeute 141.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
CCOC(=O)C(C#N)=NOC(=O)OC
Reaction #285905
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCOC(=O)C(N)C#N
Reaction #298136
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
NC1=C(N=O)C(=O)N2CCN=C2N1Cc1ccc(Cl)cc1
Reaction #323177
pink powder
Ausbeute 77.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1987_02
Nc1nc2n(c(=O)c1N=O)CCN2Cc1ccc(Cl)cc1
Reaction #323194
7-Amino-1-[(4-Chlorophenyl)Methyl]-2,3-Dihydro-6-Nitrosoimidazo-[1,2-a]Pyrimidin-5-(1H)-One
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1987_02
CC1CN2C(=O)C(N=O)=C(N)N(Cc3ccc(Cl)cc3)C2=N1
Reaction #323200
7-Amino-8-[(4-Chlorophenyl)Methyl]-2,3-Dihydro-2-Methyl-6-Nitrosoimidazo[1,2-a]Pyrimidin-5(8H)-One
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1987_02
CC1(C)CNC(=S)N1
Reaction #323203
4,4-Dimethylimidazoline-2-thione
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1987_02
CC(C)CN1C2=NC(C)(C)CN2C(=O)C(N=O)=C1N
Reaction #323205
7-Amino-2,3-dihydro-2,2-dimethyl-8-(2-methylpropyl)-6-nitrosoimidazo[1,2-a]pyrimidin-5(8H)-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1987_02
CCOC(=O)C(C#N)=NOS(C)(=O)=O
Reaction #372475
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CCOC(=O)C(N)C#N
Reaction #378009
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CCOC(=O)C(C#N)=NOS(=O)(=O)c1ccc(C)cc1
Reaction #392998
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
C=CCOC(=O)ON=C(C#N)C(=O)OCC
Reaction #408669
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CCOC(=O)C(N)C#N
Reaction #462067
title compound
Ausbeute 37.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_01
CCOC(=O)C(N)C#N
Reaction #465412
title compound
Ausbeute 74.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_02
CCOC(=O)[C@@H](N)C#N
Reaction #496009
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_06
CCOC(=O)C(C#N)NC(=O)OCc1ccccc1
Reaction #513202
ethyl 2-benzyloxycarbonylamino-2-cyanoacetate
Ausbeute 64.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_01
CCOC(=O)C(N)C#N
Reaction #653614
title compound
Ausbeute 74.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_01
CCOC(=O)C(N)C#N
Reaction #767297
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
Seite 1Weiter