部分構造検索

3281

CS(=O)(=O)c1nccc(OCC(F)(F)F)n1
Reaction #1013
2-methanesulphonyl-4-(2,2,2-trifluorethoxy)-pyrimidine
収率 87.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1c2c(c(OC)c3ccccc13)C(=O)N(c1ccc(CC(=O)O)cc1)C2
Reaction #43997
[4-(4,9-dimethoxy-1-oxo-1,3-dihydro-2H-benzo[f]isoindol-2-yl)phenyl]acetic acid
収率 15.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(C2(O)C(=O)N(c3ccccc3)N(c3ccccc3)C2=O)cc1
Reaction #51850
1,2-Diphenyl-4-hydroxy-4-(4-methylphenyl)-3,5-pyrazolidinedione
DOI: 10.6084/m9.figshare.5104873.v1
C[C@H]1COc2c(N3CCN(C)CC3)c(F)cc3c(=O)c(C(=O)O)cn1c23.C[C@H]1COc2c(N3CCN(C)CC3)c(F)cc3c(=O)c(C(=O)O)cn1c23.O
Reaction #59651
levofloxacin hemihydrate
収率 3079.7%DOI: 10.6084/m9.figshare.5104873.v1
c1ccc2c(c1)cc1ccc3cccc4ccc2c1c34
Reaction #64597
Benzo(a)pyrene
DOI: 10.6084/m9.figshare.5104873.v1
Brc1ccc(C2CC2)c(I)c1
Reaction #68754
5-bromo-2-cyclopropyliodobenzene
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cnc(Nc2cc3[nH]c(C4CC4)nc3cn2)cn1
Reaction #68933
title compound
収率 16.1%DOI: 10.6084/m9.figshare.5104873.v1
COC1=C(I)C(=O)C2C3CCC(O3)C12
Reaction #69962
4-Iodo-5-methoxy-10-oxa-tricyclo[5.2.1.0*2,6*]dec-4-en-3-one
収率 84.6%DOI: 10.6084/m9.figshare.5104873.v1
O=S([O-])[O-].[Na+].[Na+]
Reaction #82308
sodium sulfite
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #85401
compound 2
DOI: 10.6084/m9.figshare.5104873.v1
Brc1cc2c(cn1)[nH]c1ncc(I)cc12
Reaction #88591
title compound
収率 84.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C12CC3CC(CC(Br)(C3)C1)C2
Reaction #91529
compound
収率 92.8%DOI: 10.6084/m9.figshare.5104873.v1
c1ccc(-c2ccc(CC3CC4OC4C3)cc2)cc1
Reaction #93567
products
DOI: 10.6084/m9.figshare.5104873.v1
CSc1cccc(Sc2ccc(C(O)S(=O)(=O)[O-])cc2)c1.[Na+]
Reaction #155415
title compound
収率 55.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(C2=NOC(c3cc(Cl)cc(Cl)c3)(C(F)(F)F)C2S(C)(=O)=O)cc1C
Reaction #156583
4-[5-(3,5-dichloro-phenyl)-4-methanesulfonyl-5-trifluoromethyl-4,5-dihydro-isoxazol-3-yl]-2-methyl-benzoic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(C)c2nc(-c3cnc(NCCCC4CCN(C)CC4)nc3C)[nH]c2c1
Reaction #163551
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc(NCCCC2CCN(C)CC2)ncc1-c1nc2c(C)c(F)ccc2[nH]1
Reaction #163552
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1cn(C[C@H]2CCCO2)c(=N)s1.I
Reaction #165728
title compound
収率 50.0%DOI: 10.6084/m9.figshare.5104873.v1
C#Cc1nc(-c2ccc(S(=O)(=O)C(C)C)cc2)cnc1N(C(=O)OC(C)(C)C)C(=O)OC(C)(C)C
Reaction #165841
product
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cccc2[nH]cc(Br)c12
Reaction #167369
3-Bromo-1H-indole-4-carbonitrile
収率 78.4%DOI: 10.6084/m9.figshare.5104873.v1
1 ページ次のページ