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CC(C)(C)[Si](OCC1CC(Nc2nc(N)nc(O)c2[N+](=O)[O-])C1O[Si](c1ccccc1)(c1ccccc1)C(C)(C)C)(c1ccccc1)c1ccccc1
Reaction #6059
title compound
Ausbeute 64.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(Nc1nc(N)nc(O)c1[N+](=O)[O-])C(COc1ccccc1)=NO
Reaction #185508
DOI: 10.1039/C8SC04228D
CCC(CC)(Nc1nc(N)nc(O)c1[N+](=O)[O-])C(CO)=NO
Reaction #703433
nitropyrimidine
Ausbeute 48.8%DOI: 10.6084/m9.figshare.5104873.v1
CCC(CC)(Nc1nc(N)nc(O)c1[N+](=O)[O-])C(CO)=NO
Reaction #895766
DOI: 10.1039/C8SC04228D
Cc1ccc(-c2nc(N)nc(O)c2[N+](=O)[O-])o1
Reaction #964134
required product
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CCNc1nc(N)nc(O)c1[N+](=O)[O-]
Reaction #1026371
DOI: 10.1039/C8SC04228D
CC(C)(Nc1nc(N)nc(O)c1[N+](=O)[O-])C(COc1ccccc1)=NO
Reaction #1037903
DOI: 10.1039/C8SC04228D
CCOc1nc(N2CCSCC2)nc(Cl)c1[N+](=O)[O-]
Reaction #1370635
6-Ethoxy-4-chloro-5-nitro-2-thiomorpholino-pyrimidine
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CCNc1nc(N)nc(O)c1[N+](=O)[O-]
Reaction #1503347
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(-c2nc(N)nc(O)c2[N+](=O)[O-])o1
Reaction #1652953
DOI: 10.1039/C8SC04228D
CC(C)(Nc1nc(N)nc(O)c1[N+](=O)[O-])C(COc1ccccc1)=NO
Reaction #1667770
nitropyrimidine oxime
Ausbeute 48.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(Nc1nc(N)nc(O)c1[N+](=O)[O-])C(COc1ccccc1)=NO
Reaction #1667773
nitropyrimidine oxime
Ausbeute 16.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(N)CNc1nc(N)nc(O)c1[N+](=O)[O-].Cl
Reaction #1696882
monohydrochloride
Ausbeute 97.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(N)(CNc1nc(N)nc(O)c1[N+](=O)[O-])c1ccccc1.Cl
Reaction #1696883
monohydrochloride
Ausbeute 95.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(N)CNc1nc(N)nc(O)c1[N+](=O)[O-].Cl
Reaction #1701486
monohydrochloride
Ausbeute 97.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(N)(CNc1nc(N)nc(O)c1[N+](=O)[O-])c1ccccc1.Cl
Reaction #1701488
monohydrochloride
Ausbeute 95.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(-c2nc(N)nc(O)c2[N+](=O)[O-])o1
Reaction #2183838
required product
Ausbeute 67.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOc1nc(N2CCSCC2)nc(Cl)c1[N+](=O)[O-]
Reaction #2222988
DOI: 10.1039/C8SC04228D
CC(C)(C)[Si](OCC1CC(Nc2nc(N)nc(O)c2[N+](=O)[O-])C1O[Si](c1ccccc1)(c1ccccc1)C(C)(C)C)(c1ccccc1)c1ccccc1
Reaction #2235066
DOI: 10.1039/C8SC04228D
Cc1ccc(-c2nc(N)nc(O)c2[N+](=O)[O-])o1
Reaction #2294715
required product
Ausbeute 67.0%DOI: 10.6084/m9.figshare.5104873.v1