Teilstruktursuche

616074

CC(=O)CCCc1ccc([N+](=O)[O-])cc1
Reaction #370877
DOI: 10.1039/C8SC04228D
COC(=O)c1cn(CCc2ccc([N+](=O)[O-])cc2)c2c1C(SC)=NCC2
Reaction #584565
4-Methylsulfanyl-1-[2-(4-nitro-phenyl)-ethyl]-6,7-dihydro-1H-pyrrolo[3,2-c]pyridine-3-carboxylic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(C2(C#N)CCC(=O)CC2)ccc1[N+](=O)[O-]
Reaction #751020
DOI: 10.1039/C8SC04228D
COC(=O)C1CC(C#N)(c2ccc([N+](=O)[O-])c(OC)c2)CCC1=O
Reaction #1349499
5-Cyano-5-(3-methoxy-4-nitro-phenyl)-2-oxo-cyclohexanecarboxylic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #1349500
solid
Ausbeute 48.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)CCCc1ccc([N+](=O)[O-])cc1
Reaction #1676522
5-(4-nitrophenyl)-2-pentanone
Ausbeute 40.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)CCCc1ccc([N+](=O)[O-])cc1
Reaction #2069658
5-(4-nitrophenyl)-2-pentanone
Ausbeute 40.3%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1CC(C#N)(c2ccc([N+](=O)[O-])cc2)CCC1=O
Reaction #2078204
crude product 3
Ausbeute 102.2%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1CC(C#N)(c2ccc([N+](=O)[O-])c(OC)c2)CCC1=O
Reaction #2213184
DOI: 10.1039/C8SC04228D
COC(=O)C1CC(C#N)(c2ccc([N+](=O)[O-])cc2)CCC1=O
Reaction #2230948
DOI: 10.1039/C8SC04228D