部分構造検索

1170150

O=C(O)C1CN(C(=O)OCc2ccccc2)CCN1c1c([N+](=O)[O-])ccc(Cl)c1Cl
Reaction #11905
desired product
収率 43.6%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1c(Cl)c(Cl)c(Cl)c(Cl)c1Cl
Reaction #54208
pentachloronitrobenzene
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C1CN(C(=O)OCc2ccccc2)CCN1c1c([N+](=O)[O-])ccc(Cl)c1Cl
Reaction #77315
desired product
収率 43.6%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #81992
solid
収率 71.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #81993
orange solid
収率 16.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #82580
solid
収率 71.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #82581
orange solid
収率 16.0%DOI: 10.6084/m9.figshare.5104873.v1
CCC(=O)Nc1c([N+](=O)[O-])cnn1-c1ccc(Cl)c(Cl)c1Cl
Reaction #93663
4-nitro-5-propionamido-1-(2,3,4-trichlorophenyl)-pyrazole
収率 76.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C1CN(C(=O)OCc2ccccc2)CCN1c1c([N+](=O)[O-])ccc(Cl)c1Cl
Reaction #173680
DOI: 10.1039/C8SC04228D
N#Cc1cnn(-c2ccc(Cl)c(Cl)c2Cl)c1NCCCl
Reaction #244848
DOI: 10.1039/C8SC04228D
CC(=O)Nc1c(C#N)cnn1-c1ccc(Cl)c(Cl)c1Cl
Reaction #254745
DOI: 10.1039/C8SC04228D
CCOC=Nc1c(C#N)cnn1-c1ccc(Cl)c(Cl)c1Cl
Reaction #259355
DOI: 10.1039/C8SC04228D
CCOC(=O)c1c(Nc2c([N+](=O)[O-])ccc(Cl)c2Cl)sc2ccccc12
Reaction #266571
DOI: 10.1039/C8SC04228D
Nc1nc2cc(Cl)c(Cl)c(Cl)c2[nH]1
Reaction #351049
13b
DOI: 10.6084/m9.figshare.5104873.v1
Cl
Reaction #368669
DOI: 10.1039/C8SC04228D
Nc1c(C(=O)Cl)cnn1-c1ccc(Cl)c(Cl)c1Cl
Reaction #375025
DOI: 10.1039/C8SC04228D
CCOC(=O)C(Cl)Cc1c(C#N)cnn1-c1ccc(Cl)c(Cl)c1Cl
Reaction #383995
DOI: 10.1039/C8SC04228D
N#Cc1cnn(-c2ccc(Cl)c(Cl)c2Cl)c1NC(=O)CCCCl
Reaction #403458
DOI: 10.1039/C8SC04228D
O=[N+]([O-])c1ccc(Cl)c(Cl)c1Cl
Reaction #429374
2,3,4-trichloronitrobenzene
DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccc(Cl)c(Cl)c1Cl
Reaction #429375
2,3,4-trichloronitrobenzene
DOI: 10.6084/m9.figshare.5104873.v1
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