Busqueda de Subestructura

257197

CC(C)c1cccc(C(C)C)c1NC(=O)C(=O)Nc1ccccc1O
Reaction #11828
solid
Rendimiento 85.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(O)c(NC(=O)C(=O)Nc2c(C(C)C)cccc2C(C)C)c1
Reaction #11831
solid
Rendimiento 90.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(Cl)ccc1NC(=O)COCC(=O)Nc1c(C(C)C)cccc1C(C)C
Reaction #242502
DOI: 10.1039/C8SC04228D
CCOC(=O)C(=O)Nc1c(C(C)(C)C)cc(C(C)(C)C)cc1C(C)(C)C
Reaction #264137
DOI: 10.1039/C8SC04228D
CC(=O)OCC(=O)Nc1c(C(C)C)cccc1C(C)C
Reaction #335015
brown solid
Rendimiento 40.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)c1cccc(C(C)C)c1NC(=O)CO
Reaction #335016
title compound
Rendimiento 94.9%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(=O)Nc1c(C(C)(C)C)cc(C(C)(C)C)cc1C(C)(C)C
Reaction #498301
N-(2,4,6-tri-tert-butylphenyl)oxalamic acid ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)c1cccc(C(C)C)c1NC(=O)CO
Reaction #1312449
DOI: 10.1039/C8SC04228D
CC(C)c1cccc(C(C)C)c1NC(=O)COCC(=O)Nc1ccc(Cl)cc1C(=O)O
Reaction #1317333
DOI: 10.1039/C8SC04228D
CCOC(=O)C(=O)Nc1c(C(C)(C)C)cc(C(C)(C)C)cc1C(C)(C)C
Reaction #1352455
N-(2,4,6-tri-tert-butylphenyl)oxalamic acid ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)c1cccc(C(C)C)c1NC(=O)C(=O)Nc1ccccc1O
Reaction #1910367
solid
Rendimiento 85.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(O)c(NC(=O)C(=O)Nc2c(C(C)C)cccc2C(C)C)c1
Reaction #1910370
solid
Rendimiento 90.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cn(-c2ccc(Cl)cc2)nc1O
Reaction #2090330
DOI: 10.1038/s41557
CCOC(=O)c1cn(-c2ccc(Cl)cc2)nc1O
Reaction #2090399
DOI: 10.1038/s41557
CCOC(=O)c1cn(-c2ccc(Cl)cc2)nc1O
Reaction #2090453
DOI: 10.1038/s41557
CCOC(=O)C(F)c1ccc(-c2cccnc2)cc1
Reaction #2090737
DOI: 10.1038/s41557
CCOC(=O)C(F)c1ccc(-c2ccccc2)cc1
Reaction #2090810
DOI: 10.1038/s41557
CCOc1cc(Cl)c(C#N)cc1-n1cccn1
Reaction #2091010
DOI: 10.1038/s41557
CCOc1cc(Cl)c(C#N)cc1-n1cccn1
Reaction #2091065
DOI: 10.1038/s41557
CCOC(=O)c1cn(-c2ccc(Cl)cc2)nc1O
Reaction #2091144
DOI: 10.1038/s41557
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