Substructure Search

15327

CC1=c2cc(Br)ccc2=NC1=O
Reaction #7078
title compound
Yield 60.3%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)C(=O)Nc2ccc(-c3cccc(Cl)c3)cc21
Reaction #7079
title compound
Yield 25.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)C(=O)Nc2ccc(-c3cccc([N+](=O)[O-])c3)cc21
Reaction #7080
title compound
Yield 119.0%DOI: 10.6084/m9.figshare.5104873.v1
CCC1C(=O)Nc2ccc(Br)cc21
Reaction #7082
subtitled compound
DOI: 10.6084/m9.figshare.5104873.v1
CCC1(CC)C(=O)Nc2ccc(Br)cc21
Reaction #7083
subtitled compound
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
COC1(C)C(=O)Nc2ccc(Br)cc21
Reaction #7085
5-bromo-3-methoxy-3-methyl-1,3-dihydro-indol-2-one
Yield 53.7%DOI: 10.6084/m9.figshare.5104873.v1
COC1(C)C(=O)Nc2ccc(-c3cccc(Cl)c3)cc21
Reaction #7086
5-(3-chloro-phenyl)-3-methoxy-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
CC#CC1(OC)C(=O)Nc2ccc(-c3cccc(Cl)c3)cc21
Reaction #7088
title compound
Yield 15.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1Nc2ccc(Br)cc2C12CCCCC2
Reaction #7094
subtitled compound
Yield 67.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)n1cccc1-c1ccc2c(c1)C1(CCCCC1)C(=O)N2
Reaction #7095
subtitled compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)C(=O)Nc2ccc(-c3ccc(F)c(Cl)c3)cc21
Reaction #7104
title compound
Yield 30.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1Nc2ccc(Br)cc2C12CCCCC2
Reaction #9408
subtitled compound
Yield 67.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)n1cccc1-c1ccc2c(c1)C1(CCCC1)C(=O)N2
Reaction #9411
2-(1′,2′-dihydro-2′-oxospiro[cyclopentane-1,3′-[3H]indol]-5′-yl)-1H-pyrrole-1-carboxylic acid, tert-butyl ester
Yield 83.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)n1cccc1-c1ccc2c(c1)C1(CCCCC1)C(=O)N2
Reaction #9412
2-(1′,2′-dihydro-2′-oxospiro[cyclohexane-1,3′-[3H]indol]-5′-yl)-1H-pyrrole-1-carboxylic acid, tert-butyl ester
Yield 77.3%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)C(=O)Nc2ccc(-c3cccc(Cl)c3)cc21
Reaction #9417
subtitled compound
Yield 25.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)C(=O)Nc2ccc(Br)cc21
Reaction #9419
subtitled compound
Yield 92.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(-c2ccc3c(c2)C(C)(C)C(=O)N3)c1
Reaction #9420
5-(3-methoxy-phenyl)-3,3-dimethyl-1,3-dihydro-indol-2-one
Yield 31.0%DOI: 10.6084/m9.figshare.5104873.v1
CCC1(CC)C(=O)Nc2ccc(Br)cc21
Reaction #9424
5-bromo-1,3-dihydro-3,3-diethyl-[2H]-indol-2-one
DOI: 10.6084/m9.figshare.5104873.v1
Page 1Next