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13369

COc1cc(OC)c(-c2cc3ccccc3n2C(=O)OC(C)(C)C)cc1/C=C/C(=O)c1ccc(S(N)(=O)=O)cc1
Reaction #10802
title compound
Выход 40.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)c(-c2cc3ccccc3[nH]2)cc1/C=C/C(=O)c1ccc(S(N)(=O)=O)cc1
Reaction #10803
title compound
Выход 70.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)c(-c2cc3ccccc3n2C)cc1/C=C/C(=O)c1ccc(S(N)(=O)=O)cc1
Reaction #10841
title compound
Выход 90.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)NS(=O)(=O)c1ccc(C(=O)C=Cc2cc(-c3cc4ccccc4[nH]3)c(OC)cc2OC)cc1
Reaction #390281
DOI: 10.1039/C8SC04228D
CNS(=O)(=O)c1ccc(C(=O)/C=C/c2cc(-c3cc4ccccc4n3C)c(OC)cc2OC)cc1
Reaction #434527
title compound
Выход 57.0%DOI: 10.6084/m9.figshare.5104873.v1
CONS(=O)(=O)c1ccc(C(=O)/C=C/c2cc(-c3cc4ccccc4n3C)c(OC)cc2OC)cc1
Reaction #434529
title compound
Выход 94.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)c(-c2cc3ccccc3n2C)cc1/C=C/C(=O)c1ccc(S(=O)(=O)N(C)C)cc1
Reaction #434530
title compound
Выход 64.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)c(-c2cc3ccccc3[nH]2)cc1/C=C/C(=O)c1ccc(S(=O)(=O)N(C)C)cc1
Reaction #434533
title compound
Выход 12.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)c(-c2cc3ccccc3n2C)cc1/C=C/C(=O)c1ccc(S(=O)(=O)NO[Si](C)(C)C(C)(C)C)cc1
Reaction #434535
title compound
Выход 19.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)c(-c2cc3ccccc3[nH]2)cc1/C=C/C(=O)c1ccc(S(N)(=O)=O)cc1
Reaction #434540
4-{3E-[5-(1H-indol-2-yl)-2,4-dimethoxyphenyl]acryloyl}benzenesulfonamide
Выход 83.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)c(-c2cc3ccccc3n2C)cc1C=CC(=O)c1ccc(S(N)(=O)=O)cc1
Reaction #434541
4-{3-[2,4-dimethoxy-5-(1-methyl-1H-indol-2-yl)phenyl]acryloyl}benzenesulfonamide
Выход 90.2%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)NS(=O)(=O)c1ccc(C(=O)/C=C/c2cc(-c3cc4ccccc4[nH]3)c(OC)cc2OC)cc1
Reaction #434547
title compound
Выход 0.9%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)c(-c2cc3ccccc3[nH]2)cc1/C=C/C(=O)c1ccc(S(=O)(=O)NC(C)=O)cc1
Reaction #434548
title compound
Выход 62.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCC(=O)NS(=O)(=O)c1ccc(C(=O)/C=C/c2cc(-c3cc4ccccc4[nH]3)c(OC)cc2OC)cc1
Reaction #434550
title compound
Выход 75.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)c(-c2cc3ccccc3[nH]2)cc1/C=C/C(=O)c1ccc(S(=O)(=O)NCCCn2ccnc2)cc1
Reaction #434553
title compound
Выход 100.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)c(-c2cc3ccccc3[nH]2)cc1/C=C/C(=O)c1ccc(S(=O)(=O)NCC(=O)O)cc1
Reaction #434555
title compound
Выход 23.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)c(-c2cc3ccccc3[nH]2)cc1/C=C/C(=O)c1ccc(S(=O)(=O)Nc2ccccn2)cc1
Reaction #434568
title compound
Выход 44.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)c(-c2cc3ccccc3[nH]2)cc1/C=C/C(=O)c1ccc(S(=O)(=O)Nc2ccccn2)cc1
Reaction #434569
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)c(-c2cc3ccccc3n2C)cc1C=CC(=O)c1ccc(S(N)(=O)=O)cc1
Reaction #771857
DOI: 10.1039/C8SC04228D
COc1cc(OC)c(-c2cc3ccccc3[nH]2)cc1C=CC(=O)c1ccc(S(N)(=O)=O)cc1
Reaction #775228
DOI: 10.1039/C8SC04228D
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