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7265

NS(=O)(=O)c1ccc(Nc2ccccc2)cc1
Reaction #496
المردود 30.0%
C[Si](C)(C)OCCN(CCO[Si](C)(C)C)S(=O)(=O)c1ccccc1
Reaction #2934
title compound
المردود 88.0%DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(Nc1cc(F)ccc1F)c1ccccc1
Reaction #4330
2,5-difluoro-N-benzenesulphonylaniline
DOI: 10.6084/m9.figshare.5104873.v1
NS(=O)(=O)c1ccccc1
Reaction #4835
phenylsulfonamide
DOI: 10.6084/m9.figshare.5104873.v1
O=S1N=C(S(=O)(=O)c2ccccc2)c2ccccc21
Reaction #5233
benzenesulfonylbenzisothiazolone
DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(NCCCOc1cccc2nccn12)c1ccccc1
Reaction #5556
desired product
المردود 59.5%DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(c1ccccc1)n1cc(I)c2cc(F)cc(F)c21
Reaction #8210
N-Benzenesulfonyl-3-iodo-5,7-difluoroindole
المردود 87.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(Cc1c[nH]c2c(NS(=O)(=O)c3ccccc3)cccc12)[N+](=O)[O-]
Reaction #8226
3-(2-nitro-2-methylpropyl)-7-benzenesulfonamidyl-indole
المردود 71.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #8426
light purple solid
المردود 91.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(c2ccc3c(ccn3S(=O)(=O)c3ccccc3)c2)CC1
Reaction #8434
oil
المردود 66.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NC(=N)c1ccc(CNC(=O)[C@@H]2CCc3ncc(NS(=O)(=O)c4ccccc4)c(=O)n32)cc1
Reaction #11063
intermediate 17a
المردود 80.1%DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(c1ccccc1)n1cccc1
Reaction #11332
1-benzenesulfonylpyrrole
المردود 736.9%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1C[C@H](NS(=O)(=O)c2ccccc2)C(=O)[C@H]2[C@@]1(C)CC[C@H]1C(=O)O[C@H](c3ccoc3)C[C@]21C
Reaction #40606
43
المردود 98.9%DOI: 10.6084/m9.figshare.5104873.v1
CCC1(c2c[nH]c3c(NS(=O)(=O)c4ccccc4)cccc23)CCc2cc(F)ccc21
Reaction #41994
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)N(CCCNS(=O)(=O)c1ccccc1)Cc1cccc(-c2ccnc(NCCc3ccc(O)cc3)n2)c1
Reaction #43033
N-{3-[(3-{2-[2-(4-Hydroxy-phenyl)-ethylamino]-pyrimidin-4-yl}-benzyl)-methanesulfonyl-amino]-propyl}-benzenesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1
Cl.O=C(N[C@H]1CN2CCC1CC2)c1cc2ccc(N(S(=O)(=O)c3ccccc3)S(=O)(=O)c3ccccc3)cc2s1
Reaction #43765
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(N[C@@H]1CCCN2c3cc(Cl)c(N(S(=O)(=O)c4ccccc4)S(=O)(=O)c4ccccc4)cc3Oc3ccccc3[C@H]12)C(F)(F)F
Reaction #44445
trans-N-(7-chloro-2,3,4,14b-tetrahydro-8-[bis(phenylsulfonyl)amino]-1H-dibenzo[b,f]pyrido[1,2-d][1,4]oxazepin-1-yl)-2,2,2-trifluoroacetamide
المردود 105.5%DOI: 10.6084/m9.figshare.5104873.v1
O=C(N[C@@H]1CCCN2c3cc(Cl)c(NS(=O)(=O)c4ccccc4)cc3Oc3ccccc3[C@H]12)C(F)(F)F
Reaction #44446
trans-N-(7-chloro-2,3,4,14b-tetrahydro-8-[(phenylsulfonyl)amino]-1H-dibenzo[b,f]pyrido[1,2-d][1,4]oxazepin-1-yl)-2,2,2-trifluoroacetamide
المردود 43.5%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-c2csc3c(NS(=O)(=O)c4ccccc4)cnc(N)c23)ccc1NC(=O)c1cc2ccccc2n1C
Reaction #45515
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)n1c(-c2ccc(OS(=O)(=O)c3ccccc3)c3c2C(=O)NC3)cc2cc(CN3CCCCC3)ccc21
Reaction #49408
4-benzenesulfonyloxy-7-[1-(tert-butoxycarbonyl)-5-(piperidinomethyl)indol-2-yl]isoindolinone
المردود 86.0%DOI: 10.6084/m9.figshare.5104873.v1
الصفحة 1التالي