Substructure Search

O=C1Nc2ccccc2C1=O

O=C1Nc2ccc(Cl)cc2C1(c1ccccc1)c1ccccc1
Reaction #1911
5-Chloro-1,3-dihydro-3,3-diphenylindol-2-one
DOI: 10.6084/m9.figshare.5104873.v1
O=C1Nc2ccc(Cl)cc2C1(c1ccccc1)c1ccccc1
Reaction #2294
5-Chloro-1,3-dihydro-3,3-diphenylindol-2-one
DOI: 10.6084/m9.figshare.5104873.v1
O=c1[nH]c2cc(Cl)cc(Cl)c2c(=O)o1
Reaction #3199
title compound
Yield 72.0%DOI: 10.6084/m9.figshare.5104873.v1
O=c1[nH]c2cc(I)ccc2c(=O)o1
Reaction #3215
title compound
Yield 81.8%DOI: 10.6084/m9.figshare.5104873.v1
O=C1Nc2c(ccc3c2CCNC3)C1=O
Reaction #5034
6,7,8,9-tetrahydro-1H-pyrrolo[2,3-f]isoquinoline-2,3-dione
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N1C(=O)C(=O)c2cc(C)ccc21
Reaction #6455
1-acetyl-5-methylisatin
Yield 47.6%DOI: 10.6084/m9.figshare.5104873.v1
O=C1C(=O)N(c2cccc(C3OC=CO3)c2)c2ccccc21
Reaction #6699
N-[3-(1,3-dioxolyl)phenyl]isatin
DOI: 10.6084/m9.figshare.5104873.v1
O=C1C(=O)N(c2ccc(C3OC=CO3)cc2)c2ccccc21
Reaction #6703
N-[4-(1,3-dioxolyl)phenyl]isatin
DOI: 10.6084/m9.figshare.5104873.v1
O=C1C(=O)N(c2cccc(-c3ccc(OCc4ccccc4)cc3)c2)c2ccccc21
Reaction #6704
N-[3-(4-benzyloxyphenyl)phenyl]isatin
DOI: 10.6084/m9.figshare.5104873.v1
CC1(O)C(=O)Nc2ccc(Br)cc21
Reaction #7084
5-bromo-3-hydroxy-3-methyl-1,3-dihydro-indol-2-one
Yield 29.0%DOI: 10.6084/m9.figshare.5104873.v1
CC#CC1(O)C(=O)Nc2ccc(Br)cc21
Reaction #7087
5-bromo-3-hydroxy-3-prop-1-ynyl-1,3-dihydroindol-2-one
Yield 97.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(N2C(=O)C(=O)c3ccccc32)cc1
Reaction #11295
N-(4-methoxyphenyl)isatin
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2nc3ccccc3c(C(=O)O)c2c1
Reaction #11296
2-Methoxy-acridine-9-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
O=C1C(=O)N(c2cccc(C3OC=CO3)c2)c2ccccc21
Reaction #11298
N-[3-(1,3-dioxolyl)phenyl]isatin
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CN2C(=O)C(=O)c3cc(F)ccc32)cc1
Reaction #43544
5-Fluoro-1-(4-methoxy-benzyl)-1H-indole-2,3-dione
Yield 82.4%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CN2C(=O)C(=O)c3cc(F)ccc32)cc1
Reaction #43546
5-Fluoro-1-(4-methoxy-benzyl)-1H-indole-2,3-dione
Yield 80.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1Nc2ccccc2C1(O)c1ccccc1
Reaction #44898
3-hydroxy-3-phenyl-1,3-dihydro-indol-2-one
Yield 90.0%DOI: 10.6084/m9.figshare.5104873.v1
CCc1c([N+](=O)[O-])ccc2c1C(=O)C(=O)N2
Reaction #50462
5-nitro-4-ethylisatin
Yield 52.0%DOI: 10.6084/m9.figshare.5104873.v1
CCc1c([N+](=O)[O-])ccc(N)c1C(=O)O
Reaction #50463
5-nitro-6-ethyl-2-aminobenzoic acid
Yield 82.5%DOI: 10.6084/m9.figshare.5104873.v1
O=C1Cc2cc(F)ccc2N1
Reaction #52585
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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