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Oc1ccc(Br)cc1

COc1cc(N2CCN(C)CC2)c(NC(=O)OC(C)(C)C)cc1N
Reaction #418
Ausbeute 0.0%
CSCCCOc1cc(C)c(Br)c(C)c1
Reaction #43938
title compound
Ausbeute 87.0%DOI: 10.6084/m9.figshare.5104873.v1
Brc1ccc2oncc2c1
Reaction #45446
desired product
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccccc1COc1ccc(Br)cc1-c1cc(Nc2ccc(Cl)cc2)nc(N)n1
Reaction #56935
title compound
Ausbeute 57.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccccc1COc1ccc(Br)cc1-c1cc(Nc2ccc(C)cc2)nc(N)n1
Reaction #56940
title compound
Ausbeute 36.0%DOI: 10.6084/m9.figshare.5104873.v1
O=Cc1cc(Br)ccc1OCC1CO1
Reaction #67260
title compound
Ausbeute 95.7%DOI: 10.6084/m9.figshare.5104873.v1
O=Cc1cc(Br)ccc1OC[C@@H]1CO1
Reaction #67265
crude title compound
Ausbeute 107.6%DOI: 10.6084/m9.figshare.5104873.v1
O=Cc1cc(Br)ccc1OC[C@H]1CO1
Reaction #67270
crude title compound
Ausbeute 91.2%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(Br)c(C(C)O)cc1OC(C)C
Reaction #70218
title compound 37
Ausbeute 99.2%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #77542
solid
Ausbeute 48.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #77543
solid
Ausbeute 64.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #77544
solid
Ausbeute 77.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C(=S)Oc1ccc(Br)cc1C=O
Reaction #82230
5-bromo-2-[(N,N-dimethylthiocarbamoyl)oxy]benzaldehyde
Ausbeute 78.9%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C(=O)c2cc3cc(Br)ccc3o2)cc1
Reaction #82243
5-bromo-2-(4-methoxybenzoyl)benzofuran
Ausbeute 42.6%DOI: 10.6084/m9.figshare.5104873.v1
O=C1NC(=O)C(=Cc2cc(Br)cc(Br)c2O)C(=O)N1
Reaction #84047
product 1a
Ausbeute 84.6%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1cc(Br)cc(C(F)(F)F)c1)c1cc(Br)ccc1O
Reaction #174849
DOI: 10.1039/C8SC04228D
COc1cc(Br)c(C(C)O)cc1OC(C)C
Reaction #177104
DOI: 10.1039/C8SC04228D
Oc1ccc(Br)cc1C=Nc1cc(Cl)cc(Cl)c1
Reaction #177884
DOI: 10.1039/C8SC04228D
COc1cc(NC(=O)c2cc(Br)ccc2O)cc(OC)c1
Reaction #178087
DOI: 10.1039/C8SC04228D
O=c1cc(N2CCN(Cc3cc(Br)cc(Br)c3O)CC2)nc[nH]1
Reaction #178445
DOI: 10.1039/C8SC04228D
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