部分構造検索

230580

CCN(CC)CCCOc1ccc(NC=C2C(=O)Nc3cc(F)ccc32)cc1
Reaction #11606
compound
収率 61.4%DOI: 10.6084/m9.figshare.5104873.v1
O=C1Nc2cc(F)ccc2C1=CNc1ccc(OCCCN2CCCCC2)cc1
Reaction #11609
compound
収率 59.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1Nc2cc(F)ccc2C1=CNc1ccc(OCCCCN2CCCCC2)cc1
Reaction #11613
compound
収率 73.0%DOI: 10.6084/m9.figshare.5104873.v1
CCN(CC)CCCOc1ccc(NC=C2C(=O)Nc3cc(F)ccc32)cc1F
Reaction #11617
compound
収率 32.4%DOI: 10.6084/m9.figshare.5104873.v1
O=C1Nc2cc(F)ccc2C1=CNc1ccc(OCCN2CCCCC2)cc1
Reaction #11622
compound
収率 70.0%DOI: 10.6084/m9.figshare.5104873.v1
CCN(CC)CCOc1ccc(NC=C2C(=O)Nc3cc(F)ccc32)cc1
Reaction #11630
compound
収率 39.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1Nc2cc(F)ccc2C1=CNc1ccc(OCCN2CCCC2)cc1
Reaction #11635
compound
収率 48.8%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCCC(COc2ccc(NC=C3C(=O)Nc4cc(F)ccc43)cc2)C1
Reaction #11643
compound
収率 55.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(COc2cc(/C=C/c3ccc(F)cc3)ccn2)cc1
Reaction #43328
title compound
収率 61.0%DOI: 10.6084/m9.figshare.5104873.v1
O=c1cc(/C=C/c2ccc(F)cc2)ccn1-c1ccc(OCCN2CCCC2)cc1
Reaction #43329
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1ccccc1S(=O)(=O)Nc1ccc2[nH]nc(/C=C/c3ccc(F)cc3)c2c1
Reaction #53706
N-{3-[(E)-2-(4-fluorophenyl)vinyl]-1H-indazol-5-yl}-2-methylsulfonylbenzenesulfonamide
収率 29.4%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(C(=O)C(C)C)C(c1ccc(F)cc1)C1CCCN=C1OC
Reaction #57362
methyl 2-[(4-fluorophenyl)-(2-methoxy-3,4,5,6-tetrahydro-pyridin-3-yl)-methyl]-4-methyl-3-oxo-pentanoate
収率 106.5%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(C(=O)C(C)C)C(c1ccc(F)cc1)C1CCCN(C(=O)OC(C)(C)C)C1=O
Reaction #57371
methyl 1-[(1,1-dimethylethoxy)carbonyl]-β-(4-fluorophenyl)-α-(2-methyl-1-oxopropyl)-2-oxo-3-piperidinepropanoate
収率 77.4%DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)CCOc1c(C(=O)O)ccc2[nH]nc(/C=C/c3ccc(F)cc3)c12
Reaction #62380
title compound
収率 55.1%DOI: 10.6084/m9.figshare.5104873.v1
Fc1ccc(/C=C/c2cccc3c4c([nH]c23)C2CCN(CC2)C4)c(F)c1
Reaction #66074
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cl.Fc1ccc(/C=C/c2nc3ccccc3n2-c2ccccn2)cc1
Reaction #79174
titled compound
DOI: 10.6084/m9.figshare.5104873.v1
OCC(=C(c1ccc(F)cc1)c1ccc(F)cc1)c1nnn(C(c2ccccc2)(c2ccccc2)c2ccccc2)n1
Reaction #173372
DOI: 10.1039/C8SC04228D
COc1ccc(CNc2ncc(C#N)c3sc4cc(C=Cc5ccc(F)cc5)ccc4c23)cc1
Reaction #182646
DOI: 10.1039/C8SC04228D
CC(=O)C1=C(c2ccc(F)cc2)c2ccc(NC(=O)OC(C)(C)C)cc2OC1(C)C
Reaction #186808
DOI: 10.1039/C8SC04228D
CN1CCN(Nc2ccc(C=C3c4ccc(F)cc4OCc4c(F)cccc43)cc2[N+](=O)[O-])CC1
Reaction #187376
DOI: 10.1039/C8SC04228D
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