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Brc1ccc2c(c1)CCN2

CN1CC[C@@]2(C)c3cc(Br)c(O)cc3N(C)[C@@H]12
Reaction #1864
cis-(±)-5-Bromo-1,2,3,3a,8,8a-hexahydro-1,3a,8-trimethylpyrrolo[2,3-b]indol-6-ol
DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)c1ccccc1N1CCc2cc(Br)ccc21
Reaction #4102
2-(5-bromo-indolin-1-yl)benzamide
DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(C2=Nc3ccccc3N3CCc4cc(Br)cc2c43)CC1
Reaction #4103
product
Ausbeute 57.0%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccccc1N1CCc2cc(Br)ccc21
Reaction #4118
product
Ausbeute 55.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(C(=O)Nc2ccccc2N2CCc3cc(Br)ccc32)CC1
Reaction #4121
product
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2c(c1)N=C(N1CCN(C)CC1)c1cc(Br)cc3c1N2CC3
Reaction #4127
product
Ausbeute 53.9%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(N2CCc3cc(Br)ccc32)c(N)c1.Cl
Reaction #4130
product
Ausbeute 39.0%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1cc(Br)ccc1N1CCc2cc(Br)ccc21
Reaction #4131
product
Ausbeute 68.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(C(=O)Nc2cc(Br)ccc2N2CCc3cc(Br)ccc32)CC1
Reaction #4132
product
Ausbeute 84.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(C2=Nc3cc(Br)ccc3N3CCc4cc(Br)cc2c43)CC1
Reaction #4133
product
Ausbeute 70.3%DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)c1ccccc1N1CCc2cc(Br)ccc21
Reaction #4160
2-(5-bromo-indolin-1-yl)benzamide
DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(C2=Nc3ccccc3N3CCc4cc(Br)cc2c43)CC1
Reaction #4161
product
Ausbeute 57.0%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccccc1N1CCc2cc(Br)ccc21
Reaction #4176
product
Ausbeute 55.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(C(=O)Nc2ccccc2N2CCc3cc(Br)ccc32)CC1
Reaction #4179
product
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2c(c1)N=C(N1CCN(C)CC1)c1cc(Br)cc3c1N2CC3
Reaction #4185
product
Ausbeute 53.9%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(N2CCc3cc(Br)ccc32)c(N)c1.Cl
Reaction #4188
product
Ausbeute 39.0%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1cc(Br)ccc1N1CCc2cc(Br)ccc21
Reaction #4189
product
Ausbeute 68.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(C(=O)Nc2cc(Br)ccc2N2CCc3cc(Br)ccc32)CC1
Reaction #4190
product
Ausbeute 84.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(C2=Nc3cc(Br)ccc3N3CCc4cc(Br)cc2c43)CC1
Reaction #4191
product
Ausbeute 70.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N1CCc2cc(Br)cc(N)c21
Reaction #5023
compound
Ausbeute 32.2%DOI: 10.6084/m9.figshare.5104873.v1
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