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970820

CCC1c2cc(F)ccc2-c2cc(C)ccc2N1S(=O)(=O)c1ccc(OC)cc1
Reaction #175822
DOI: 10.1039/C8SC04228D
CC1c2cc(Cl)ccc2-c2cc(Br)ccc2N1S(=O)(=O)c1ccc(O)cc1
Reaction #178693
DOI: 10.1039/C8SC04228D
CCC1c2cc(F)ccc2-c2cc(-c3ccsc3)ccc2N1S(=O)(=O)c1ccc(OC)cc1
Reaction #237655
DOI: 10.1039/C8SC04228D
O=S(=O)(c1ccc(O)cc1)N1c2ccc(Br)cc2-c2ccccc2C1c1ccccc1
Reaction #270503
DOI: 10.1039/C8SC04228D
CC1c2ccccc2-c2cc(Br)ccc2N1S(=O)(=O)c1ccc(O)c(F)c1
Reaction #272918
DOI: 10.1039/C8SC04228D
O=S(=O)(c1ccc(O)c(Br)c1)N1c2ccc(Br)cc2-c2ccccc2C1c1ccccc1
Reaction #376415
DOI: 10.1039/C8SC04228D
CCC1c2cc(F)ccc2-c2cc(Br)ccc2N1S(=O)(=O)c1ccc(O)cc1
Reaction #766462
DOI: 10.1039/C8SC04228D
CC1c2ccccc2-c2cc(Br)ccc2N1S(=O)(=O)c1ccc(O)cc1
Reaction #2233961
DOI: 10.1039/C8SC04228D
CCC1c2cc(F)ccc2-c2cc(-c3ccccc3)ccc2N1S(=O)(=O)c1ccc(OC)cc1
Reaction #2242510
DOI: 10.1039/C8SC04228D
COc1ccc(S(=O)(=O)N2c3ccc(Br)cc3-c3ccccc3C2C)cc1
Reaction #2268970
title compound
Ausbeute 48.5%DOI: 10.6084/m9.figshare.5104873.v1
CC1c2ccccc2-c2cc(Br)ccc2N1S(=O)(=O)c1ccc(O)cc1
Reaction #2268971
title compound
Ausbeute 68.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(S(=O)(=O)N2c3ccc(Br)cc3-c3ccccc3C2c2ccccc2)cc1
Reaction #2268974
title compound
Ausbeute 28.0%DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(c1ccc(O)cc1)N1c2ccc(Br)cc2-c2ccccc2C1c1ccccc1
Reaction #2268975
title compound
Ausbeute 86.0%DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(c1ccc(O)c(Br)c1)N1c2ccc(Br)cc2-c2ccccc2C1c1ccccc1
Reaction #2268976
title compound
Ausbeute 63.0%DOI: 10.6084/m9.figshare.5104873.v1
CCC1c2ccccc2-c2cc(Br)ccc2N1S(=O)(=O)c1ccc(OC)cc1
Reaction #2268983
title compound
Ausbeute 87.3%DOI: 10.6084/m9.figshare.5104873.v1
CCC1c2ccccc2-c2cc(Br)ccc2N1S(=O)(=O)c1ccc(OC)c(C)c1
Reaction #2268985
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCC1c2ccccc2-c2cc(Br)ccc2N1S(=O)(=O)c1ccc(O)cc1
Reaction #2268991
title compound
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1
c1ccc2c(c1)CNc1ccccc1-2
Reaction #2269026
dihydrophenanthridine
DOI: 10.6084/m9.figshare.5104873.v1
CCC1c2cc(F)ccc2-c2cc(Br)ccc2N1S(=O)(=O)c1ccc(O)cc1
Reaction #2269027
4-[(2-bromo-6-ethyl-8-fluorophenanthridin-5(6H)-yl)sulfonyl]phenol
Ausbeute 38.3%DOI: 10.6084/m9.figshare.5104873.v1
CCC1c2cc(F)ccc2-c2cc(-c3ccccc3)ccc2N1S(=O)(=O)c1ccc(OC)cc1
Reaction #2269032
title compound
Ausbeute 52.8%DOI: 10.6084/m9.figshare.5104873.v1
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