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1122924

C=Cc1ccccc1-c1cccc(S(=O)(=O)c2cc(C(=N)NC(=O)OC(C)(C)C)sc2SC)c1
Reaction #197607
DOI: 10.1039/C8SC04228D
CSc1sc(C(=N)NC(=O)OC(C)(C)C)cc1S(=O)(=O)c1cc(O)cc(-c2ccccc2Cl)c1
Reaction #223081
DOI: 10.1039/C8SC04228D
COc1cc(C)c(-c2cccc(S(=O)(=O)c3cc(C(=N)NC(=O)OC(C)(C)C)sc3SC)c2)c(N)c1
Reaction #242334
DOI: 10.1039/C8SC04228D
CSc1sc(C(=N)NC(=O)OC(C)(C)C)cc1S(=O)(=O)c1cccc(-c2c(C)cccc2CO)c1
Reaction #265363
DOI: 10.1039/C8SC04228D
CSc1sc(C(=N)NC(=O)OC(C)(C)C)cc1S(=O)(=O)c1cccc(-c2cccc(N)c2)c1
Reaction #267344
DOI: 10.1039/C8SC04228D
CSc1sc(C(=N)NC(=O)OC(C)(C)C)cc1S(=O)(=O)c1cccc(-c2c(C)cccc2N)c1
Reaction #405519
DOI: 10.1039/C8SC04228D
C=Cc1ccc(-c2cccc(S(=O)(=O)c3cc(C(=N)NC(=O)OC(C)(C)C)sc3SC)c2)cc1
Reaction #781621
DOI: 10.1039/C8SC04228D
CSc1sc(C(=N)NC(=O)OC(C)(C)C)cc1S(=O)(=O)c1cccc(-c2cccc(C(=O)OC(C)C)c2C)c1
Reaction #810205
title compound
Ausbeute 49.3%DOI: 10.6084/m9.figshare.5104873.v1
CSc1sc(C(=N)NC(=O)OC(C)(C)C)cc1S(=O)(=O)c1cccc(-c2c(C)cccc2C(=O)OC(C)(C)C)c1
Reaction #810207
title compound
Ausbeute 58.1%DOI: 10.6084/m9.figshare.5104873.v1
CSc1sc(C(=N)NC(=O)OC(C)(C)C)cc1S(=O)(=O)c1cccc(-c2c(C)cccc2CO)c1
Reaction #810210
title compound
Ausbeute 40.0%DOI: 10.6084/m9.figshare.5104873.v1
CSc1sc(C(=N)NC(=O)OC(C)(C)C)cc1S(=O)(=O)c1cccc(-c2cc(CO)ccc2C)c1
Reaction #810215
title compound
Ausbeute 67.0%DOI: 10.6084/m9.figshare.5104873.v1
CSc1sc(C(=N)NC(=O)OC(C)(C)C)cc1S(=O)(=O)c1cccc(-c2cnccc2C)c1
Reaction #810217
title compound
Ausbeute 71.5%DOI: 10.6084/m9.figshare.5104873.v1
CSc1sc(C(=N)NC(=O)OC(C)(C)C)cc1S(=O)(=O)c1cccc(-c2cccnc2Cl)c1
Reaction #810218
title compound
Ausbeute 59.2%DOI: 10.6084/m9.figshare.5104873.v1
CSc1sc(C(=N)NC(=O)OC(C)(C)C)cc1S(=O)(=O)c1cc(O)cc(Br)c1
Reaction #810225
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CSc1sc(C(=N)NC(=O)OC(C)(C)C)cc1S(=O)(=O)c1cc(O)cc(-c2ccccc2Cl)c1
Reaction #810226
title compound
Ausbeute 24.0%DOI: 10.6084/m9.figshare.5104873.v1
CSc1sc(C(=N)NC(=O)OC(C)(C)C)cc1S(=O)(=O)c1cccc(-c2c(C)cccc2N)c1
Reaction #810234
title compound
Ausbeute 28.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(OC)c1cc(-c2cccc(S(=O)(=O)c3cc(C(=N)NC(=O)OC(C)(C)C)sc3SC)c2)ccc1O
Reaction #810236
title compound
Ausbeute 28.0%DOI: 10.6084/m9.figshare.5104873.v1
CSc1sc(C(=N)NC(=O)OC(C)(C)C)cc1S(=O)(=O)c1cccc(-c2cccc(C(O)C(F)(F)F)c2)c1
Reaction #810239
(Imino-{5-methylsulfanyl-4-[3′-(2,2,2-trifluoro-1-hydroxy-ethyl)-biphenyl-3-sulfonyl]-thiophen-2-yl}-methyl)-carbamic acid tert-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1
C=Cc1ccccc1-c1cccc(S(=O)(=O)c2cc(C(=N)NC(=O)OC(C)(C)C)sc2SC)c1
Reaction #810244
{Imino-[5-methylsulfanyl-4-(2′-vinyl-biphenyl-3-sulfonyl)-thiophen-2-yl]-methyl}-carbamic acid tert-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1
C=Cc1ccc(-c2cccc(S(=O)(=O)c3cc(C(=N)NC(=O)OC(C)(C)C)sc3SC)c2)cc1
Reaction #810246
title compound
Ausbeute 45.0%DOI: 10.6084/m9.figshare.5104873.v1
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