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Clc1ccc(Cl)c(Cl)n1

Clc1cc(Cl)c(Cl)nc1Cl
Reaction #81577
2,3,5,6-tetrachloropyridine
Ausbeute 62.0%DOI: 10.6084/m9.figshare.5104873.v1
Clc1cc(Cl)c(Nc2cc(C3CC3)[nH]n2)nc1Cl
Reaction #163102
title compound
Ausbeute 12.8%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)Oc1cc(Nc2nc(Cl)c(Cl)cc2[N+](=O)[O-])n[nH]1
Reaction #163112
title compound
Ausbeute 27.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)Oc1cc(Nc2nc(Cl)c([N+](=O)[O-])cc2Cl)n[nH]1
Reaction #163113
title compound
Ausbeute 18.1%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cc(Cl)c(Nc2cc(C3CC3)[nH]n2)nc1Cl
Reaction #163124
title compound
Ausbeute 43.9%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cc(Cl)c(Cl)nc1Cl
Reaction #163125
title compound
Ausbeute 99.2%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cc(Cl)c(Cl)nc1Cl
Reaction #163126
title compound
Ausbeute 71.1%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1cc(Cl)c(Cl)nc1Cl
Reaction #163127
title compound
Ausbeute 18.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(Nc2nc(Cl)c(C#N)cc2Cl)n[nH]1
Reaction #163134
title compound
Ausbeute 59.8%DOI: 10.6084/m9.figshare.5104873.v1
Clc1cc(Cl)c(Cl)nc1Cl
Reaction #177302
DOI: 10.1039/C8SC04228D
Clc1cnc(Cl)c(Cl)c1
Reaction #190248
DOI: 10.1039/C8SC04228D
CN(c1ccc([N+](=O)[O-])cc1C(F)(F)F)c1c(Cl)c(Cl)nc(Cl)c1Cl
Reaction #196200
DOI: 10.1039/C8SC04228D
N#Cc1cc(Cl)c(Cl)nc1Cl
Reaction #197993
DOI: 10.1039/C8SC04228D
Clc1cc(Cl)c(Cl)nc1Cl
Reaction #202369
DOI: 10.1039/C8SC04228D
O=c1[nH]c(Cl)c(C(F)(F)F)cc1Cl
Reaction #205094
DOI: 10.1039/C8SC04228D
COCC1COC(=O)N1c1ccc(C(=O)N2CCN(c3nc(Cl)c(Cl)cc3Cl)CC2)cc1
Reaction #209565
DOI: 10.1039/C8SC04228D
Clc1cc(Cl)c(Cl)nc1Cl
Reaction #215549
2,3,5,6 -tetrachloropyridine
Ausbeute 92.2%DOI: 10.6084/m9.figshare.5104873.v1
Clc1cc(Cl)c(Cl)nc1Cl
Reaction #215550
2,3,5,6-tetrachloropyridine
Ausbeute 93.4%DOI: 10.6084/m9.figshare.5104873.v1
Clc1cc(Cl)c(Cl)nc1Cl
Reaction #215551
2,3,5,6-tetrachloropyridine
Ausbeute 93.1%DOI: 10.6084/m9.figshare.5104873.v1
Clc1cc(Cl)c(Cl)nc1Cl
Reaction #215552
2,3,5,6-tetrachloropyridine
Ausbeute 94.1%DOI: 10.6084/m9.figshare.5104873.v1
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