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Clc1cccc(Cl)n1

Clc1ccc(Nc2ccccc2)c(Cl)n1
Reaction #243
Ausbeute 0.0%
CC(C)(C)OC(=O)Nc1cc(C(=O)O)cc(Cl)n1
Reaction #244
Ausbeute 0.0%
Clc1ccc(Nc2ccccc2)c(Cl)n1
Reaction #252
Ausbeute 0.0%
Clc1ccc(Nc2ccccc2)c(Cl)n1
Reaction #253
Ausbeute 0.0%
Clc1ccc(Nc2ccccc2)c(Cl)n1
Reaction #254
Ausbeute 92.1%
Clc1ccc(N2CCOCC2)c(Cl)n1
Reaction #574
Ausbeute 0.0%
Clc1ccc(N2CCOCC2)c(Cl)n1
Reaction #575
Ausbeute 0.0%
C#CCn1c(-c2cc(Cl)nc(Cl)c2)nn(C(C)(C)C)c1=O
Reaction #3716
2-(t-butyl)-5-(2,6-dichloro-4-pyridyl)-4-propargyl-1,2,4-triazolin-3-one
DOI: 10.6084/m9.figshare.5104873.v1
O=C(NC(=O)c1cc(F)c(Cl)nc1Cl)NC1CC1
Reaction #10425
title compound
Ausbeute 98.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)NCCNc1nc(Cl)ccc1[N+](=O)[O-]
Reaction #42790
N-(2-(6-chloro-3-nitropyridin-2-ylamino)ethyl)acetamide
DOI: 10.6084/m9.figshare.5104873.v1
COc1nc(Cl)c(C(=O)O)cc1F
Reaction #43406
product
Ausbeute 65.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1cc(F)c(=O)[nH]c1Cl
Reaction #44258
desired product
Ausbeute 47.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Nc1cccc(-c2cncc(Nc3cc(Cl)nc(Cl)c3)n2)c1
Reaction #44541
title compound
Ausbeute 7.8%DOI: 10.6084/m9.figshare.5104873.v1
CNc1cc(Cl)nc(Cl)c1
Reaction #45374
2,6-Dichloro-4-methylamino-pyridine
DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc(C(F)(F)F)c(Cl)n1
Reaction #46227
6-chloro-5-(trifluoromethyl)pyridin-2-amine
Ausbeute 46.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1nc(Cl)ccc1[N+](=O)[O-]
Reaction #48365
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H](C)Nc1nc(Cl)ccc1[N+](=O)[O-]
Reaction #49806
compound A
Ausbeute 69.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(COc1cccc(Cl)[n+]1[O-])CC(C)(C)C
Reaction #49969
2-chloro-6-(2,4,4-trimethypentyloxy) pyridine N-oxide
DOI: 10.6084/m9.figshare.5104873.v1
CC(CCOc1cccc(Cl)[n+]1[O-])CC(C)(C)C
Reaction #49970
2-chloro-6-(3,5,5trimethylhexyloxy)pyridine N-oxide
DOI: 10.6084/m9.figshare.5104873.v1
[OH-]
Reaction #49971
hydroxide
DOI: 10.6084/m9.figshare.5104873.v1
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