部分構造検索

17037

Cc1cccc(-c2nn3c(c2-c2ccc(F)cc2)CC[C@H]3CO)n1
Reaction #8374
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC#Cc1ccc(NC(=O)c2ccccc2NCc2ccc(=O)[nH]c2)cc1C(F)(F)F
Reaction #8995
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCc1ccc(-c2ccc(COCCCP(=O)(O)O)nc2-c2ccccc2)cc1
Reaction #40830
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C1C(I)CC[C@H]2CCC[C@@H](c3ccc(Cl)cc3)N12
Reaction #44645
(6S,9aR)-6-(4-chlorophenyl)-3-iodooctahydroquinolizin-4-one
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](O)[C@H]1COC[C@@H](c2ccc(Cl)cc2)N1
Reaction #44655
titled compound
収率 86.1%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2c(c3c1c(=O)c1cc4ccccc4nc1n3C)[C@@H](OC(C)=O)[C@@H](OC(=O)CN)C(C)(C)O2
Reaction #46317
(±)-cis-1-(Acetyloxy)-6methoxy-3,3,14-trimethyl-7-oxo-2,3,7,14-tetrahydro-1H-benzo[b]chromeno[6,5-g][1,8]naphthyridin-2-yl aminoacetate
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](CO)Oc1cc(Oc2ccc(S(C)(=O)=O)cc2)cc(C(=O)Nc2ccn(C)n2)c1
Reaction #48775
title compound
収率 84.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cnc(NC(=O)c2cc(O)cc(O[C@@H](C)CO)c2)cn1
Reaction #48794
title compound
収率 65.6%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(O)cc(O[C@@H](C)CO)c1
Reaction #48802
title compound
収率 47.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](CO)Oc1cc(O)cc(C(=O)Nc2ccn(C)n2)c1
Reaction #48809
desired compound
収率 74.4%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](CO)Oc1cc(Oc2ccc(S(=O)(=O)N(C)C)cc2)cc(C(=O)Nc2ccn(C)n2)c1
Reaction #48820
title compound
収率 45.5%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc(Oc2cc(O[C@@H](C)CO)cc(C(=O)Nc3cc[nH]n3)c2)cc1
Reaction #48826
oil
収率 111.3%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](CO)Oc1cc(Oc2ccc(-c3ncon3)cc2)cc(C(=O)Nc2ccn(C)n2)c1
Reaction #48833
title compound
収率 84.5%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](CO)Oc1cc(O)cc(C(=O)Nc2ccn(C)n2)c1
Reaction #48853
desired compound
収率 64.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](CO)Oc1cc(Oc2ccc(-c3cc[nH]n3)cc2)cc(C(=O)Nc2ccn(C)n2)c1
Reaction #48871
title compound
収率 82.4%DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(Nc1ccc2[nH]nc(-c3ccccc3)c2c1)c1cccc(F)c1
Reaction #53639
3-fluoro-N-(3-phenyl-1H-indazol-5-yl)benzenesulfonamide
収率 31.8%DOI: 10.6084/m9.figshare.5104873.v1
Cc1n[nH]c2ccc(NS(=O)(=O)c3cccc(F)c3)cc12
Reaction #53643
3-fluoro-N-(3-methyl-1H-indazol-5-yl)-benzenesulfonamide
収率 59.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1n[nH]c2ccc(NS(=O)(=O)c3ccccc3S(C)(=O)=O)cc12
Reaction #53645
2-methylsulfonyl-N-(3-methyl-1H-indazol-5-yl)benzenesulfonamide
収率 30.8%DOI: 10.6084/m9.figshare.5104873.v1
Cc1n[nH]c2ccc(NS(=O)(=O)c3ccc(Cl)c(Cl)c3)cc12
Reaction #53665
3,4-dichloro-N-(3-methyl-1H-indazol-5-yl)benzenesulfonamide
収率 80.1%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)/C=C/c1n[nH]c2ccc(NS(=O)(=O)c3ccccc3S(C)(=O)=O)cc12
Reaction #53709
methyl (E)-3-[5(2-methylsulfonylbenzenesulfonylamino)-1H-indazol-3-yl]-acrylate
収率 15.6%DOI: 10.6084/m9.figshare.5104873.v1
1 ページ次のページ