Участвует в 91 реакциях

4509

O=Cc1ccc2c(c1)CCO2
Reaction #3097
title compound
Выход 60.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=Cc1cc(Br)c2c(c1)CCO2
Reaction #43451
desired compound
Выход 91.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=Cc1cc(Br)c2c(c1)CCO2
Reaction #43639
desired compound
Выход 91.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(=O)/C=C/c1ccc2c(c1)CCO2
Reaction #51207
title product
Выход 84.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
O=C1Nc2ccc(Cl)cc2C1=Cc1ccc2c(c1)CCO2
Reaction #52637
5-Chloro-3-(2,3-dihydro-benzofuran-5-ylmethylene)-1,3-dihydroindol-2-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
O=C1Nc2ccc(F)cc2C1=Cc1ccc2c(c1)CCO2
Reaction #52677
3-(2,3-dihydrobenzofuran-5-ylmethylene)-5-fluoro-1,3-dihydroindol-2-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
O=C1Nc2ccccc2C1=Cc1ccc2c(c1)CCO2
Reaction #52696
3-(2,3-dihydrobenzofuran-5-ylmethylene)-1,3-dihydroindol-2-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
Cc1cccc2c1C(=Cc1ccc3c(c1)CCO3)C(=O)N2
Reaction #52699
3-(2,3-dihydrobenzofuran-5-ylmethylene)-4-methyl-1,3-dihydroindol-2-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
O=C1Nc2ncccc2C1=Cc1ccc2c(c1)CCO2
Reaction #52703
3-(2,3-dihydrobenzofuran-5-ylmethylene)-1,3-dihydropyrrolo[2,3-b]pyridin-2-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
O=C1Nc2ccc(Br)cc2C1=Cc1ccc2c(c1)CCO2
Reaction #52728
5-bromo-3-(2,3-dihydrobenzofuran-5-ylmethylene)-1,3-dihydroindol-2-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
O=Cc1ccc2c(c1)CCO2
Reaction #82850
title compound
Выход 60.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
O=Cc1ccc2c(c1)CCO2
Reaction #175015
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)C(=O)Nc1cccc(C2CCN(Cc3ccc4c(c3)CCO4)CC2)c1
Reaction #184987
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC(=O)C(=Cc1ccc2c(c1)CCO2)N=[N+]=[N-]
Reaction #209316
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=Cc1ccc2c(c1)CCO2
Reaction #221692
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
FC(F)(F)c1nnc2ccc(N3CCN(Cc4ccc5c(c4)CCO5)CC3)nn12
Reaction #222468
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCOC(=O)C=Cc1ccc2c(c1)CCO2
Reaction #238101
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=C1Nc2ccc(F)cc2C1=Cc1ccc2c(c1)CCO2
Reaction #238824
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COC(=O)CCc1cccc(CNCc2ccc3c(c2)CCO3)c1
Reaction #267301
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
O=Cc1ccc2c(c1)CCO2
Reaction #288436
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
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