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CCc1ccccc1

CC(C)(C)c1cc(SCCCC(=O)O)cc(C(C)(C)C)c1O
Reaction #5596
4-[[3,5-bis(1,1-dimethylethyl)-4-hydroxy phenyl]thio]butanoic acid
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CCc1ccc(S(=O)(=O)Nc2ccc(Cl)cc2C(=O)c2ccccc2)cc1
Reaction #47165
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CCc1ccc(S(=O)(=O)Nc2ccc(Cl)cc2C(=O)c2ccnc(C)c2)cc1
Reaction #57873
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CCc1ccc(S(=O)(=O)Nc2ccc(Cl)cc2C(=O)c2cccnc2C)cc1
Reaction #57878
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CCc1ccc(S(=O)(=O)Nc2ccc(Cl)cc2C(=O)c2ccc(C)nc2)cc1
Reaction #57883
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N1CCC(Nc2ccc(C(=O)c3ccccc3F)c(N)n2)CC1
Reaction #58389
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC[C@@H](N)c1ccc(S(=O)(=O)NC(C)(C)C)cc1
Reaction #70624
(R)-4-(1-aminopropyl)-N-tert-butylbenzenesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](N)c1ccc(S(=O)(=O)NC(C)(C)C)cc1
Reaction #70632
(R)-4-(1-Amino-ethyl)-N-tert-butyl-benzenesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1
CCN(CC)S(=O)(=O)c1ccc(CCC(=O)OC)cc1
Reaction #83256
product
DOI: 10.6084/m9.figshare.5104873.v1
NS(=O)(=O)c1ccc(CCN(CC(=O)O)Cc2nccn2CC(=O)O)cc1
Reaction #84613
2-(2-(((carboxymethyl)(4-sulfamoylphenethyl)amino)methyl)-1H-imidazol-1-yl)acetic acid
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(C(=O)CBr)cc(S(N)(=O)=O)c1
Reaction #96065
2-bromo-3'-methyl-5'-sulfamoylacetophenone
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CCc1ccc(OCc2cc(OC)c(CO)s2)cc1F
Reaction #156277
title compound
Ausbeute 108.6%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CCc1ccc(OCc2cc(OC)c(C=O)s2)cc1F
Reaction #156278
title compound
Ausbeute 50.8%DOI: 10.6084/m9.figshare.5104873.v1
Clc1cccc(Nc2ccc3ncc(Cc4ccc5ncccc5c4)n3n2)c1
Reaction #156360
title compound
DOI: 10.6084/m9.figshare.5104873.v1
c1ccc(Nc2ccc3ncc(Cc4ccc5ncccc5c4)n3n2)cc1
Reaction #156361
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1cc(Cl)cnc1N1CCCC1c1ccccc1
Reaction #159639
title compound ( D98 )
Ausbeute 108.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1cc(Cl)cnc1N1CCCC1Cc1ccccc1
Reaction #159640
title compound ( D100 )
Ausbeute 97.8%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(C2(NC(=O)c3cc(Cl)cnc3N3CCCC3c3ccccc3)CC2)cc1
Reaction #159668
title compound ( D142 )
Ausbeute 79.4%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(C2(NC(=O)c3cc(Cl)cnc3N3CCC(c4ccccc4)C3)CC2)cc1
Reaction #159669
title compound ( D143 )
Ausbeute 51.3%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(C2(NC(=O)c3cc(Cl)cnc3N3CCCC3Cc3ccccc3)CC2)cc1
Reaction #159670
title compound ( D144 )
Ausbeute 61.2%DOI: 10.6084/m9.figshare.5104873.v1
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