Teilstruktursuche

1414698

CC(=O)N1CCc2cc([N+](=O)[O-])cc(C#N)c21
Reaction #5025
compound
Ausbeute 66.7%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1cc([N+](=O)[O-])cc2c1NCC2
Reaction #5026
compound
Ausbeute 77.1%DOI: 10.6084/m9.figshare.5104873.v1
O=C1Cc2cc([N+](=O)[O-])ccc2N1
Reaction #46400
5-nitro oxindole
Ausbeute 98.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc2c(c1)CC(=O)N2
Reaction #46401
5-amino-oxindole
Ausbeute 50.5%DOI: 10.6084/m9.figshare.5104873.v1
CCc1c([N+](=O)[O-])ccc2c1C(=O)C(=O)N2
Reaction #50462
5-nitro-4-ethylisatin
Ausbeute 52.0%DOI: 10.6084/m9.figshare.5104873.v1
CCc1c([N+](=O)[O-])ccc(N)c1C(=O)O
Reaction #50463
5-nitro-6-ethyl-2-aminobenzoic acid
Ausbeute 82.5%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc2c(c1)CC(=O)N2
Reaction #52582
title compound
Ausbeute 60.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1Cc2cc([N+](=O)[O-])ccc2N1
Reaction #52586
5-nitro-2-oxindole
Ausbeute 70.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1Cc2cc([N+](=O)[O-])ccc2N1
Reaction #52648
5-nitro-2-oxindole
Ausbeute 70.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc2c(c1)CC(=O)N2
Reaction #52649
5-amino-2-oxindole
Ausbeute 60.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N1C(=O)Cc2cc([N+](=O)[O-])ccc21
Reaction #53074
1-acetyl-5-nitro-2-indolinone
DOI: 10.6084/m9.figshare.5104873.v1
COC(=C1C(=O)N(C(C)=O)c2ccc([N+](=O)[O-])cc21)c1ccccc1
Reaction #53075
1-acetyl-3-(1-methoxy-1-phenyl-methylidene)-5-nitro-2-indo-linone
DOI: 10.6084/m9.figshare.5104873.v1
O=C1Nc2ccc([N+](=O)[O-])cc2/C1=C(/Nc1ccc(Cl)cc1)c1ccccc1
Reaction #53076
(Z)-3-[1-(4-chlorophenylamino)-1-phenyl-methylidene]-5-nitro-2-indolinone
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(N/C(=C2\C(=O)Nc3ccc([N+](=O)[O-])cc32)c2ccccc2)cc1
Reaction #53077
(Z)-3-[1-(4-methoxyphenylamino)-1-phenyl-methylidene]-5-nitro-2-indolinone
DOI: 10.6084/m9.figshare.5104873.v1
O=C1Nc2ccc([N+](=O)[O-])cc2/C1=C(/Nc1ccc([N+](=O)[O-])cc1)c1ccccc1
Reaction #53079
(Z)-3-[1-(4-nitrophenylamino)-1-phenyl-methylidene]-5-nitro-2-indolinone
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=C1C(=O)N(C(C)=O)c2ccc([N+](=O)[O-])cc21)c1ccccc1
Reaction #53080
1-acetyl-3-(1-ethoxy-1-phenyl-methylidene)-5-nitro-2-indolinone
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(N/C(=C2\C(=O)Nc3ccc([N+](=O)[O-])cc32)c2ccccc2)cc1
Reaction #53081
(Z)-3-[1-(4-cyanophenylamino)-1-phenyl-methylidene]-5-nitro-2-indolinone
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cccc(N/C(=C2\C(=O)Nc3ccc([N+](=O)[O-])cc32)c2ccccc2)c1
Reaction #53082
(Z)-3-[1-(3-cyanophenylamino)-1-phenyl-methylidene]-5-nitro-2-indolinone
DOI: 10.6084/m9.figshare.5104873.v1
O=C1Nc2ccc([N+](=O)[O-])cc2/C1=C(/Nc1ccc(C(=O)O)cc1)c1ccccc1
Reaction #53084
(Z)-3-[1-(4-carboxy-phenylamino)-1-phenyl-methylidene]-5-nitro-2-indolinone
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=C1C(=O)Nc2ccc([N+](=O)[O-])cc21)c1ccccc1
Reaction #53085
3-(1-ethoxy-1-phenyl-methylidene)-5-nitro-2-indolinone
DOI: 10.6084/m9.figshare.5104873.v1
Seite 1Weiter