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990542

COc1ncc(B2OC(C)(C)C(C)(C)O2)cc1NS(=O)(=O)c1ccc(F)cc1F
Reaction #67107
title compound
Ausbeute 84.1%DOI: 10.6084/m9.figshare.5104873.v1
COc1ncc(-c2cc(-c3nnc(CN4C[C@@H](C)N(C(C)C)[C@@H](C)C4)o3)c3cn[nH]c3c2)cc1NS(=O)(=O)c1ccc(F)cc1F
Reaction #67164
title compound
Ausbeute 2.5%DOI: 10.6084/m9.figshare.5104873.v1
COc1ncc(-c2cc(-c3ncc(CN4CCN(C(C)C)CC4)o3)c3cnn(S(=O)(=O)c4ccccc4)c3c2)cc1NS(=O)(=O)c1ccc(F)cc1F
Reaction #179101
DOI: 10.1039/C8SC04228D
COc1ncc(-c2cc(-c3ncc(CN4CC(C)OC(C)C4)o3)c3cnn(S(=O)(=O)c4ccccc4)c3c2)cc1NS(=O)(=O)c1ccc(F)cc1F
Reaction #401675
DOI: 10.1039/C8SC04228D
COc1ncc(B2OC(C)(C)C(C)(C)O2)cc1NS(=O)(=O)c1ccc(F)cc1F
Reaction #607705
title compound
Ausbeute 84.1%DOI: 10.6084/m9.figshare.5104873.v1
COc1ncc(B2OC(C)(C)C(C)(C)O2)cc1NS(=O)(=O)c1ccc(F)cc1F
Reaction #607742
title compound
Ausbeute 84.1%DOI: 10.6084/m9.figshare.5104873.v1
COc1ncc(-c2cc(-c3ncc(CN4C[C@@H](C)O[C@@H](C)C4)o3)c3cnn(S(=O)(=O)c4ccccc4)c3c2)cc1NS(=O)(=O)c1ccc(F)cc1F
Reaction #607743
title compound
Ausbeute 34.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ncc(-c2cc(-c3ncc(CN4CCN(C(C)C)CC4)o3)c3cnn(S(=O)(=O)c4ccccc4)c3c2)cc1NS(=O)(=O)c1ccc(F)cc1F
Reaction #607744
title compound
Ausbeute 26.5%DOI: 10.6084/m9.figshare.5104873.v1
COc1ncc(-c2cc(-c3nnc(CN4C[C@@H](C)N(C(C)C)[C@@H](C)C4)o3)c3cn[nH]c3c2)cc1NS(=O)(=O)c1ccc(F)cc1F
Reaction #607817
title compound
Ausbeute 2.5%DOI: 10.6084/m9.figshare.5104873.v1
COc1ncc(B2OC(C)(C)C(C)(C)O2)cc1NS(=O)(=O)c1ccc(F)cc1F
Reaction #798543
2,4-difluoro-N-(2-methoxy-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-3-yl)benzenesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1
COc1ncc(B2OC(C)(C)C(C)(C)O2)cc1NS(=O)(=O)c1ccc(F)cc1F
Reaction #1048718
DOI: 10.1039/C8SC04228D
COc1ncc(B2OC(C)(C)C(C)(C)O2)cc1NS(=O)(=O)c1ccc(F)cc1F
Reaction #1139692
title compound
Ausbeute 84.2%DOI: 10.6084/m9.figshare.5104873.v1
COc1ncc(-c2c(N)ncnc2N[C@@H](C)c2nn3ccc(C)c3c(=O)n2-c2ccccc2)cc1NS(=O)(=O)c1ccc(F)cc1F
Reaction #1140027
title compound
Ausbeute 52.2%DOI: 10.6084/m9.figshare.5104873.v1
COc1ncc(-c2cc(NC(=O)c3csc(CN4CC(C)OC(C)C4)n3)c3cnn(S(=O)(=O)c4ccc(C)cc4)c3c2)cc1NS(=O)(=O)c1ccc(F)cc1F
Reaction #1217777
DOI: 10.1039/C8SC04228D
COc1ncc(-c2cc(NC(=O)c3csc(CN4C[C@@H](C)O[C@@H](C)C4)n3)c3cnn(S(=O)(=O)c4ccc(C)cc4)c3c2)cc1NS(=O)(=O)c1ccc(F)cc1F
Reaction #1782921
title compound
Ausbeute 51.4%DOI: 10.6084/m9.figshare.5104873.v1
COc1ncc(-c2cc(NC(=O)c3csc(CN4C[C@@H](C)O[C@@H](C)C4)n3)c3cnn(C)c3c2)cc1NS(=O)(=O)c1ccc(F)cc1F
Reaction #1782971
title compound
Ausbeute 25.7%DOI: 10.6084/m9.figshare.5104873.v1
COc1ncc(B2OC(C)(C)C(C)(C)O2)cc1NS(=O)(=O)c1ccc(F)cc1F
Reaction #1999507
title compound
Ausbeute 84.1%DOI: 10.6084/m9.figshare.5104873.v1
COc1ncc(-c2cc(-c3ncc(CN4C[C@@H](C)O[C@@H](C)C4)o3)c3cnn(S(=O)(=O)c4ccccc4)c3c2)cc1NS(=O)(=O)c1ccc(F)cc1F
Reaction #1999508
title compound
Ausbeute 34.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ncc(B2OC(C)(C)C(C)(C)O2)cc1NS(=O)(=O)c1ccc(F)cc1F
Reaction #2123237
title compound
Ausbeute 84.1%DOI: 10.6084/m9.figshare.5104873.v1
COc1ncc(-c2cc(-c3ncc(CN4C[C@@H](C)O[C@@H](C)C4)o3)c3cnn(S(=O)(=O)c4ccccc4)c3c2)cc1NS(=O)(=O)c1ccc(F)cc1F
Reaction #2123238
title compound
Ausbeute 34.0%DOI: 10.6084/m9.figshare.5104873.v1
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