部分構造検索

1173516

CC1(C)Nc2cccc3c(N=Nc4c([N+](=O)[O-])ccc5ccccc45)ccc(c23)N1
Reaction #56102
desired compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)Nc2cccc3c(N=Nc4ccc([N+](=O)[O-])c5cc6ccccc6cc45)ccc(c23)N1
Reaction #56103
desired compound
DOI: 10.6084/m9.figshare.5104873.v1
Cl
Reaction #182132
DOI: 10.1039/C8SC04228D
CCN(CC12CCCN1CCC2)c1ccc([N+](=O)[O-])c2ccccc12
Reaction #210237
DOI: 10.1039/C8SC04228D
O=[N+]([O-])c1ccc(I)c2ccccc12
Reaction #252890
DOI: 10.1039/C8SC04228D
CCOC(=O)C(=O)Nc1cc([N+](=O)[O-])c2ccccc2c1NC(=O)C(=O)OCC
Reaction #262201
DOI: 10.1039/C8SC04228D
Nc1ccc([N+](=O)[O-])c2ccccc12
Reaction #344780
4-nitro-1-naphthylamine
DOI: 10.6084/m9.figshare.5104873.v1
Cl.NNc1ccc([N+](=O)[O-])c2ccccc12
Reaction #347079
expected product
DOI: 10.6084/m9.figshare.5104873.v1
CCN(CC12CCCN1CCC2)c1ccc([N+](=O)[O-])c2ccccc12
Reaction #348102
desired compound
収率 30.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C[C@H]1CSC(=Nc2ccc([N+](=O)[O-])c3ccccc23)N1
Reaction #363652
(4S)-2-(4-nitro-1-naphthylimino)-4-isobutyl-1,3-thiazolidine
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C[C@H]1CSC(=Nc2ccc([N+](=O)[O-])c3ccccc23)N1CC(C)C
Reaction #363653
(4S)-2-(4-nitro-1-naphthylimino)-3,4-diisobutyl-1,3-thiazolidine
DOI: 10.6084/m9.figshare.5104873.v1
CCC(C)[C@H]1CSC(=Nc2ccc([N+](=O)[O-])c3ccccc23)N1
Reaction #363667
(4S)-2-(4-nitro-1-naphthylimino)-4-(2-butyl)-1,3-thiazolidine
DOI: 10.6084/m9.figshare.5104873.v1
Nc1cc([N+](=O)[O-])c2c([N+](=O)[O-])c(N)cc([N+](=O)[O-])c2c1[N+](=O)[O-]
Reaction #458534
2,6-diamino-1,4,5,8-tetranitronaphthalene
DOI: 10.6084/m9.figshare.5104873.v1
O=C1C2CCCN2C(=O)N1c1ccc([N+](=O)[O-])c2ccccc12
Reaction #521247
title compound
収率 19.9%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(=O)Nc1cc([N+](=O)[O-])c2ccccc2c1NC(=O)C(=O)OCC
Reaction #564944
1,2-Diethoxalylamino-4-nitronaphthalene
DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc([N+](=O)[O-])c2c(F)cccc12
Reaction #810831
compound 209B
収率 27.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc([N+](=O)[O-])c2c(Cl)cccc12
Reaction #810835
compound 214A
収率 32.0%DOI: 10.6084/m9.figshare.5104873.v1
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
CCOP(=O)(Cn1c(=O)c(=O)[nH]c2cc([N+](=O)[O-])c3ccccc3c21)OCC
Reaction #813714
(6-Nitro-2,3-dioxo-1,2,3,4-tetrahydrobenzo[f]quinoxalin-1-yl)-methanephosphonic acid diethyl ester
DOI: 10.6084/m9.figshare.5104873.v1
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