子结构搜索

C=Cc1cccc(N)c1

CCOC(=O)CC1=CCC(C)(C)c2ccc(N=Nc3ccc(C(=O)OCC)cc3)cc21

title compounds

DOI: 10.6084/m9.figshare.5104873.v1

CC(=O)C(=Cc1cccc([N+](=O)[O-])c1)C(C)=O

1-acetyl-1-(3-nitrobenzyliden)acetone

收率 53.5%DOI: 10.6084/m9.figshare.5104873.v1

CC(=O)C1=C(C)N=C(c2ccccc2)NC1c1cccc([N+](=O)[O-])c1

5-acetyl-4-methyl-6-(3-nitrophenyl)-2-phenyl-1,6-dihydropyrimidine

收率 31.0%DOI: 10.6084/m9.figshare.5104873.v1

COc1cc(CC(=O)Nc2cccc(/C=C/c3cccc(C)c3)c2)ccc1OCCNC(=O)OC(C)(C)C

4-[2-(tert-butoxycarbonylamino)-ethoxy]-3-methoxy-N-[3-[(E)-2-(3-methylphenyl)vinyl]phenyl]phenylacetamide

收率 152.4%DOI: 10.6084/m9.figshare.5104873.v1

COc1cc(CC(=O)Nc2cccc(CCc3cccc(C)c3)c2)ccc1OCCNC(=O)OC(C)(C)C

4-[2-(tert-butoxycarbonylamino)ethoxy]-3-methoxy-N-[3-[2-(3-methylphenyl)ethyl]phenyl]phenylacetamide

收率 79.7%DOI: 10.6084/m9.figshare.5104873.v1

COc1c(CC=O)cccc1[N+](=O)[O-]

Reaction #44141

收率 54.0%DOI: 10.6084/m9.figshare.5104873.v1

$CN(C)C(=O)CN(c1ccc(N/C(=C2\C(=O)Nc3ccc([N+](=O)[O-])cc32)c2ccccc2)cc1)S(=O)(=O)c1ccccc1$

Reaction #53179

(Z)-3-{1-[4-(N-dimethylaminocarbonylmethyl-N-phenylsulphonyl-amino)-phenylamino]-1-phenyl-methylidene}-5-nitro-2-indolinone

DOI: 10.6084/m9.figshare.5104873.v1

$Cc1ccc(S(=O)(=O)N(CC(=O)N(C)C)c2ccc(N/C(=C3\C(=O)Nc4ccc([N+](=O)[O-])cc43)c3ccccc3)cc2)cc1$

Reaction #53180

(Z)-3-{1-[4-(N-dimethylaminocarbonylmethyl-N-(p-tolylsulphonyl)-amino)-phenylamino]-1-phenyl-methylidene}-5-nitro-2-indolinone

DOI: 10.6084/m9.figshare.5104873.v1

C=C(C)c1cc([N+](=O)[O-])ccc1F

Reaction #59100

1-fluoro-4-nitro-2-(prop-1-en-2-yl)benzene

DOI: 10.6084/m9.figshare.5104873.v1

CC1(c2cc([N+](=O)[O-])ccc2F)CO1

Reaction #59101

2-(2-fluoro-5-nitrophenyl)-2-methyloxirane

DOI: 10.6084/m9.figshare.5104873.v1

C[Si](C)(C)CCOCn1ccc2c(-c3cnn(C(CC#N)c4cccc([N+](=O)[O-])c4)c3)ncnc21

Reaction #69225

3-(3-nitrophenyl)-3-[4-(7-[2-(trimethylsilyl)ethoxy]methyl-7H-pyrrolo[2,3-d]pyrimidin-4-yl)-1H-pyrazol-1-yl]propanenitrile

DOI: 10.6084/m9.figshare.5104873.v1

Nc1ccc(NCC=Cc2cc(N)ccc2N)cc1

Reaction #75428

4-[3-(2,5-diaminophenyl)allylamino]aniline

DOI: 10.6084/m9.figshare.5104873.v1

CCOC(=O)C=Cc1cc(NN=CC(=O)C(F)(F)F)ccc1Cl

Reaction #76774

ethyl 2-chloro-5-(3,3,3-trifluoro-2-oxopropylidenehydrazino)cinnamate

收率 97.5%DOI: 10.6084/m9.figshare.5104873.v1

CCOC(=O)C=Cc1cc(NN)ccc1Cl

Reaction #76775

ethyl 2-chloro-5-hydrazinocinnamate

收率 34.5%DOI: 10.6084/m9.figshare.5104873.v1

COc1cc(OC)c(Cl)c(N(COCC[Si](C)(C)C)C(=O)N(C)c2cc(Nc3ccc(C4CCN(C(=O)OC(C)(C)C)CC4)cc3N)ncn2)c1Cl

Reaction #86420

收率 37.0%DOI: 10.6084/m9.figshare.5104873.v1

CCCN(C)C(=O)Nc1cc(C2=CCCC2)ccc1[N+](=O)[O-]

Reaction #90965

3-(5-(cyclopent-1-en-1-yl)-2-nitrophenyl)-1-methyl-1-propylurea

收率 75.7%DOI: 10.6084/m9.figshare.5104873.v1

CCCN(C)C(=O)Nc1cc(C2=CCCC2)ccc1N

Reaction #90966

3-(2-amino-5-(cyclopent-1-en-1-yl)phenyl)-1-methyl-1-propylurea

收率 78.4%DOI: 10.6084/m9.figshare.5104873.v1

O=C(Cl)C=Cc1cccc([N+](=O)[O-])c1

Reaction #95085

收率 91.0%DOI: 10.6084/m9.figshare.5104873.v1

CCCCCCCCCC(C)NC(=O)C=Cc1cccc([N+](=O)[O-])c1

Reaction #95086

收率 83.0%DOI: 10.6084/m9.figshare.5104873.v1

CC=Cc1cccc2c1OC(CC)C(=O)N2C(=O)c1ccc(OC)cc1OC

Reaction #163528

4-(2,4-dimethoxyphenylcarbonyl)-2-ethyl-8-(prop-1-enyl)-2H-benzo[b][1,4]oxazin-3(4H)-one

收率 84.0%DOI: 10.6084/m9.figshare.5104873.v1

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