Teilstruktursuche

581313

N#Cc1ccc(N2C=CC(N)=C([N+](=O)[O-])C2)cc1
Reaction #6451
N-(4-cyanophenyl)-4-amino-3-nitropyridine
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(Nc2ccncc2N)cc1
Reaction #6452
3-Amino-4-(4'-cyanophenyl)aminopyridine
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(=O)N1C2=C([N+](=O)[O-])C=C(Br)CC2CCC1CC(=O)OC
Reaction #80761
title compound
Ausbeute 106.7%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CC1CCc2cc(Br)cc3[nH]c(=O)c(=O)n1c23
Reaction #80762
title compound
Ausbeute 49.0%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])/C=C1/CCCc2ccccc2N1
Reaction #167711
title compound
DOI: 10.6084/m9.figshare.5104873.v1
NCC1CCCc2ccccc2N1
Reaction #167712
crude title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=Cc1ccccc1C(F)(F)F
Reaction #173404
DOI: 10.1039/C8SC04228D
O=[N+]([O-])C=C1CN=C(c2ccccc2Cl)c2cc([N+](=O)[O-])ccc2N1
Reaction #174241
DOI: 10.1039/C8SC04228D
CNC(=C[N+](=O)[O-])CCCCCCO
Reaction #207240
DOI: 10.1039/C8SC04228D
NC1=C([N+](=O)[O-])C(=O)NC1=Cc1ccccc1
Reaction #207323
DOI: 10.1039/C8SC04228D
O=[N+]([O-])C(=NO)C1=Nc2ccc(Cl)cc2C(c2ccccc2F)=NC1
Reaction #215031
7-Chloro-5-(2-fluorophenyl)-N-hydroxy-α-nitro-3H-1,4-benzodiazepin-2-methanimine
DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])C(=NO)C1=Nc2ccc(Cl)cc2C(c2ccccc2F)=[N+]([O-])C1
Reaction #215032
7-Chloro-5-(2-fluorophenyl)-N-hydroxy-α-nitro-3H-1,4 -benzodiazepine-2-methanimine 4-oxide
DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])C(=NO)C1=Nc2ccc(Cl)cc2C(c2ccccc2F)=NC1
Reaction #215369
7-Chloro-5-(2-fluorophenyl)-N-hydroxy-α-nitro-3H-1,4-benzodiazepine-2-methanimine
DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])C(=NO)C1=Nc2ccc(Cl)cc2C(c2ccccc2F)=[N+]([O-])C1
Reaction #215370
7-Chloro-5-(2-fluorophenyl)-N-hydroxy-α-nitro-3 H-1,4-benzodiazepine-2-methanimine 4-oxide
DOI: 10.6084/m9.figshare.5104873.v1
CC1=CC(c2ccccc2C(F)(F)F)C([N+](=O)[O-])=C(C)N1
Reaction #247180
DOI: 10.1039/C8SC04228D
O=[N+]([O-])C=C1CN=C(c2ccccc2)c2cc(Cl)sc2N1
Reaction #272319
DOI: 10.1039/C8SC04228D
CCOc1nccc2c1C(c1ccc(C#N)cc1OC)C([N+](=O)[O-])=C(C)N2
Reaction #280938
DOI: 10.1039/C8SC04228D
CC1(c2ccc3c(c2)C(c2ccccc2)=NCC(=C[N+](=O)[O-])N3)OCCO1
Reaction #281370
DOI: 10.1039/C8SC04228D
O=[N+]([O-])C=C1CN=C(c2ccccc2)c2cc(Cl)ccc2N1
Reaction #284964
DOI: 10.1039/C8SC04228D
CC(=O)OCCOC(=O)C1=C(C)NC(C)=C([N+](=O)[O-])C1c1ccccc1Cl
Reaction #323753
β-Acetoxyethyl 1,4-dihydro-2,6-dimethyl-3-nitro-4-(2-chlorophenyl)-pyridine-5-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
Seite 1Weiter