部分構造検索

1180377

CC1(C)Nc2cccc3c(N=Nc4c([N+](=O)[O-])ccc5ccccc45)ccc(c23)N1
Reaction #56102
desired compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCCNc1c([N+](=O)[O-])cc(Br)c2ccccc12
Reaction #186414
DOI: 10.1039/C8SC04228D
CCOC(=O)C(=O)Nc1c([N+](=O)[O-])cc(C#N)c2ccccc12
Reaction #286098
DOI: 10.1039/C8SC04228D
O=c1[nH]c2c3ccccc3ccc2n(O)c1=O
Reaction #552489
4-hydroxy-benzo[f]quinoxaline-2,3(1H,4H)-dione
収率 65.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(=O)Nc1c([N+](=O)[O-])cc(C#N)c2ccccc12
Reaction #552490
4-Cyano-1-ethoxalylamino-2-nitronaphthalene
DOI: 10.6084/m9.figshare.5104873.v1
O=c1[nH]c2c3ccccc3c(Br)cc2n(O)c1=O
Reaction #552492
title compound
収率 65.1%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cccc2c(N)c([N+](=O)[O-])ccc12
Reaction #564952
1-amino-5-cyano-2-nitronaphthalene
収率 80.0%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cccc2c(N)c(N)ccc12
Reaction #564953
1,2-diamino-5-cyanonaphthalene
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cccc2c(N)c(N)ccc12
Reaction #760261
DOI: 10.1039/C8SC04228D
CCOP(=O)(CNc1c([N+](=O)[O-])cc([N+](=O)[O-])c2ccccc12)OCC
Reaction #813712
product
収率 68.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOP(=O)(CNc1c(N)cc([N+](=O)[O-])c2ccccc12)OCC
Reaction #813713
product
収率 21.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CNc2c([N+](=O)[O-])cc(Br)c3ccccc23)c(OC)c1
Reaction #831202
title compound
収率 78.6%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1cc([N+](=O)[O-])c2ccccc2c1Nc1ccc(OC(F)(F)F)c(Cl)c1
Reaction #934916
1-(3-chloro-4-trifluoromethoxyphenylamino)-2,4-dinitronaphthalene
収率 93.5%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CN(c1c([N+](=O)[O-])cc([N+](=O)[O-])c2ccccc12)S(=O)(=O)c1ccc(C)cc1
Reaction #948680
product
収率 76.0%DOI: 10.6084/m9.figshare.5104873.v1
CNc1c([N+](=O)[O-])cc(Br)c2ccccc12
Reaction #1028539
DOI: 10.1039/C8SC04228D
O=c1[nH]c2c3ccccc3ccc2n(O)c1=O
Reaction #1120113
4-hydroxy-benzo[f]quinoxaline-2,3(1H,4H)-dione
収率 65.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(=O)Nc1c([N+](=O)[O-])cc(C#N)c2ccccc12
Reaction #1120114
4-Cyano-1-ethoxalylamino-2-nitronaphthalene
DOI: 10.6084/m9.figshare.5104873.v1
O=c1[nH]c2c3ccccc3c(Br)cc2n(O)c1=O
Reaction #1120116
title compound
収率 65.1%DOI: 10.6084/m9.figshare.5104873.v1
O=c1[nH]c2c3ccccc3ccc2n(O)c1=O
Reaction #1177257
4-hydroxy-benzo[f]quinoxaline-2,3(1H,4H)-dione
収率 65.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(=O)Nc1c([N+](=O)[O-])cc(C#N)c2ccccc12
Reaction #1177258
4-Cyano-1-ethoxalylamino-2-nitronaphthalene
DOI: 10.6084/m9.figshare.5104873.v1
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