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1332716

CCOC(=O)C(=CNc1ccc(F)cc1F)C(=O)c1c(F)cc(F)c(F)c1C
Reaction #1385
ethyl 2-(2-methyl-3,4,6-trifluorobenzoyl)-3-(2,4-difluorophenyl)aminoacrylate
Rendimiento 87.1%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cn(-c2ccc(F)cc2F)c2cc(F)c(F)c(C)c2c1=O
Reaction #1386
ethyl 1-(2,4-difluorophenyl)-5-methyl-6,7-difluoro-1,4-dihydro-4-oxoquinoline-3-carboxylate
Rendimiento 67.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1=C(c2ccccc2)c2ccc(O)cc2C1=O
Reaction #46152
title compound
Rendimiento 58.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1=C(c2ccccc2)c2ccc(OCCCc3ccccc3)cc2C1=O
Reaction #46153
title compound
Rendimiento 85.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1=C(c2ccccc2)c2ccc(OCCCc3ccccc3)cc2C1=O
Reaction #46154
title compound
Rendimiento 85.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1=C(c2ccccc2)c2ccc(OCCN3CCOCC3)cc2C1=O
Reaction #46156
title compound
Rendimiento 128.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)[NH-].O=C([O-])C1C(=O)c2cc(O)ccc2C1c1ccccc1
Reaction #46163
5-hydroxy-3-oxo-1-phenylindane-2-carboxylate isopropyl amide
Rendimiento 4150.9%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)[NH-].O=C([O-])C1=C(c2ccccc2)c2ccc(OCCN3CCOCC3)cc2C1=O
Reaction #46164
6-(2-morpholine-4-yl ethoxy)-1-oxo-3-phenyl-1H-indene-2-carboxylate isopropyl amide
Rendimiento 99.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1=C(c2ccccc2)c2ccc(C)cc2C1=O
Reaction #46171
5-methyl-3-oxo-1-phenyl-indene-2-carboxylate ethyl ester
Rendimiento 27.5%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1=C(c2ccccc2)c2ccc(CBr)cc2C1=O
Reaction #46172
6-bromomethyl-1-oxo-3-phenyl-1H-indene-2-carboxylate ethyl ester
Rendimiento 36.7%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1=C(c2ccccc2)c2ccc(OCCCc3ccccc3)cc2C1=O
Reaction #46174
title compound
Rendimiento 75.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C([O-])C1=C(c2ccccc2)c2ccc(OCCCc3ccccc3)cc2C1=O.[NH-]C1CCCCC1
Reaction #46175
title compound
Rendimiento 59.8%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1=C(c2ccccc2)c2ccc(O)cc2C1=O
Reaction #47799
titled compound
Rendimiento 61.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1=C(c2ccccc2)c2ccc(OCCCc3ccccc3)cc2C1=O
Reaction #47807
titled compound
Rendimiento 85.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1=C(c2ccccc2)c2ccc(OCCN3CCOCC3)cc2C1=O
Reaction #47809
titled compound
Rendimiento 506.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1=C(c2ccccc2)c2ccc(OCCN3CCOCC3)cc2C1(O)c1ccccc1
Reaction #47810
titled compound
Rendimiento 44.1%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1=C(c2ccccc2)c2ccc(C)cc2C1=O
Reaction #47812
titled compound
Rendimiento 27.5%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1=C(c2ccccc2)c2ccc(CBr)cc2C1=O
Reaction #47813
titled compound
Rendimiento 36.7%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1=C(c2ccccc2)c2ccc(OCCCc3ccccc3)cc2C1=O
Reaction #47817
titled compound
Rendimiento 62.1%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1=C(c2ccccc2)c2ccc(OCCCc3ccccc3)cc2C1(O)c1ccccc1
Reaction #47818
titled compound
Rendimiento 90.3%DOI: 10.6084/m9.figshare.5104873.v1
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