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383525

CCCN(C(=O)Nc1ccc(-c2ccccc2S(=O)(=O)NC(C)(C)C)cc1)N(C(=O)OC(C)(C)C)c1cccc(C#N)c1
Reaction #50917
406
Выход 75.6%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H](Cc1ccc(-c2ccccc2S(=O)(=O)NC(C)(C)C)cc1)NC(=O)c1c(Cl)cccc1Cl
Reaction #52909
title compound
Выход 76.5%DOI: 10.6084/m9.figshare.5104873.v1
CCCc1ccc(S(=O)(=O)NC(C)(C)C)c(B(O)O)c1
Reaction #64544
titled compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCc1ccc(S(=O)(=O)NC(C)(C)C)c(-c2ccc(CO)cc2)c1
Reaction #64545
titled compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCCc1nn(-c2cc([N+](=O)[O-])ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(C)(C)C)cc1F
Reaction #64567
title compound
Выход 52.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCc1nn(-c2cc([N+](=O)[O-])ccc2Cl)c(=O)n1Cc1ccc(-c2cc(CCC)ccc2S(=O)(=O)NC(C)(C)C)cc1F
Reaction #64572
title compound
Выход 43.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(-c2ccccc2S(=O)(=O)NC(C)(C)C)cc1F
Reaction #64575
title compound
Выход 92.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCc1cc(C(=O)OCC)nn1Cc1ccc(-c2ccccc2S(N)(=O)=O)cc1
Reaction #158842
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(Cc1ccc(-c2ccccc2S(=O)(=O)NC(C)(C)C)cc1)NC(=O)c1c(Cl)cccc1Cl
Reaction #195724
DOI: 10.1039/C8SC04228D
CCCN(C(=O)Nc1ccc(-c2ccccc2S(=O)(=O)NC(C)(C)C)cc1)N(C(=O)OC(C)(C)C)c1cccc(C#N)c1
Reaction #282616
DOI: 10.1039/C8SC04228D
CC(C)(C)NS(=O)(=O)c1ccccc1B(O)O
Reaction #344750
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCCc1nn(-c2cc(NC(=O)CC)ccc2Cl)c(C#N)c1Cc1ccc(-c2ccccc2S(=O)(=O)NC(C)(C)C)cc1F
Reaction #344751
title compound
Выход 77.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCc1ccc(S(=O)(=O)NC(C)(C)C)c(B(O)O)c1
Reaction #344770
title compound
Выход 100.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)NS(=O)(=O)c1ccccc1-c1ccc(N)cc1
Reaction #390233
DOI: 10.1039/C8SC04228D
CC(C)(C)NS(=O)(=O)c1ccccc1B(O)O
Reaction #1124870
2-Borono-N-tert-butylbenzenesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)NS(=O)(=O)c1ccccc1-c1ccc2nc(N)nc(C(=O)N3Cc4ccccc4C3)c2c1
Reaction #1124871
2-[2-Amino-4-(1,3-dihydroisoindole-2-carbonyl)quinazolin-6-yl]-N-tert-butylbenzenesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H](Cc1ccc(-c2ccccc2S(=O)(=O)NC(C)(C)C)cc1)NC(=O)c1c(Cl)cccc1Cl
Reaction #1147586
title compound
Выход 76.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)NS(=O)(=O)c1ccccc1B(O)O
Reaction #1149833
desired compound
Выход 87.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)NS(=O)(=O)c1ccccc1-c1ccc(N)cc1
Reaction #1149836
title compound
Выход 41.4%DOI: 10.6084/m9.figshare.5104873.v1
CCCc1nc(CC)c(C(=O)CCc2ccccc2Oc2ccccc2)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(C)(C)C)cc1F
Reaction #1165222
yellow foam
Выход 72.0%DOI: 10.6084/m9.figshare.5104873.v1
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