子结构搜索

39390

O=C(COc1ccccc1)NC1C(=O)N2C(C(=O)OC(c3ccccc3)c3ccccc3)=C(OS(=O)(=O)c3ccc(Br)cc3)CS[C@H]12
Reaction #5643
title compound
收率 54.1%DOI: 10.6084/m9.figshare.5104873.v1
C/C=C\C1=C(C(=O)OC(c2ccccc2)c2ccccc2)N2C(=O)C(NC(=O)COc3ccccc3)[C@H]2SC1
Reaction #5644
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)C[C@H]1C[C@@H](COS(=O)(=O)c2ccc(Br)cc2)OC(C)(C)O1
Reaction #6550
product
收率 144.4%DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(c1cc(F)c(Br)cc1F)N1CCOCC1
Reaction #44352
sub-title compound
DOI: 10.6084/m9.figshare.5104873.v1
Fc1cc(Br)ccc1S
Reaction #44356
sub-title compound
收率 92.2%DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(c1ccc(Br)cc1C(F)(F)F)N1CCOCC1
Reaction #44362
sub-title compound
DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(S(=O)(=O)c2ccc(Br)cc2)CC1
Reaction #46232
required product
DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(c1ccc(Br)cc1)N1CCC[C@@H]1CO
Reaction #46238
(R)-(1-(4-bromophenylsulfonyl)pyrrolidin-2-yl)methanol
收率 90.6%DOI: 10.6084/m9.figshare.5104873.v1
CNS(=O)(=O)c1ccc(Br)cc1
Reaction #46246
4-bromo-N-methyl-benzenesulfonamide
收率 96.8%DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccccc1)c1cc(Cl)ccc1NS(=O)(=O)c1ccc(Br)cc1
Reaction #47174
title compound
收率 98.4%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CCCC=C(c1cccnc1)c1ccc2c(c1)CC(NS(=O)(=O)c1ccc(Br)cc1)C2
Reaction #50391
Methyl 6-(2-(4-bromobenzenesulphonylamino)indan-5-yl)-6-(3-pyridyl)hex-5-enoate
DOI: 10.6084/m9.figshare.5104873.v1
CN([C@H]1CC[C@H](O)CC1)S(=O)(=O)c1ccc(Br)cc1
Reaction #53826
trans-4-Bromo-N-(4-hydroxy-cyclohexyl)-N-methyl-benzenesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2c3c(ccc2n1)OC[C@H](COS(=O)(=O)c1ccc(Br)cc1)O3
Reaction #56750
title compound
收率 76.9%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H](NS(=O)(=O)c1ccc(Br)cc1)C(C)C
Reaction #57558
methyl N-[(4-bromophenyl)sulfonyl]-L-valinate
收率 101.1%DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccncc1)c1cc(Cl)ccc1NS(=O)(=O)c1ccc(Br)cc1
Reaction #57807
4-Bromo-N-[4-chloro-2-(pyridine-4-carbonyl)-phenyl]-benzenesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1cccnc1)c1cc(Cl)ccc1NS(=O)(=O)c1ccc(Br)cc1
Reaction #57815
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1cccnc1)c1cc(F)c(F)cc1NS(=O)(=O)c1ccc(Br)cc1
Reaction #57818
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(C(=O)c2cc(Cl)ccc2NS(=O)(=O)c2ccc(Br)c(F)c2)cn1
Reaction #57820
title compound
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #57823
10-ethyl acetate
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccncc1)c1cc(Cl)ccc1NS(=O)(=O)c1ccc(Br)cc1
Reaction #57833
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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