#8105021

O=C1NC(=O)c2c1c(-c1ccc(CO)cc1)cc1[nH]c3ccc(O)cc3c21
Reaction #11120
9-hydroxy-4-(4-hydroxymethylphenyl)pyrrolo[3,4-c]carbazole-1,3(2H,6H)-dione
Выход 34.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCOC(=O)c1c(-c2ccc(CO)cc2)c(-c2ccc(Cl)cc2)n(-c2ccc(S(N)(=O)=O)cc2)c1C
Reaction #46932
5-(4-chloro-phenyl)-4-(4-hydroxymethyl-phenyl)-2-methyl-1-(4-sulfamoyl-phenyl)-1H-pyrrole-3-carboxylic Acid Ethyl Ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Nc1c(-c2ccccc2CO)cc(Br)c2c1C(=O)NC2=O
Reaction #49277
3-amino-4-(hydroxymethylphenyl)-6-bromophthalimide
Выход 64.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CSc1ccc(C2=C(c3ccc(CO)cc3)CCC2)cc1
Reaction #65807
1-[2-(4-hydroxymethylphenyl)cyclopenten-1-yl]-4-(methylthio)benzene
Выход 92.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
Cc1ccc(NC(=O)C2(c3ccc4c(c3)OCO4)CC2)cc1-c1ccc(CO)cc1
Reaction #67449
1-(benzo[d][1,3]dioxol-5-yl)-N-(4′-(hydroxymethyl)-6-methylbiphenyl-3-yl)cyclopropanecarboxamide
Выход 59.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
Cc1ccc(NC(=O)C2(c3ccc4c(c3)OCO4)CC2)cc1-c1ccc(CO)cc1
Reaction #170918
1-(benzo[d][1,3]dioxol-5-yl)-N-(4′-(hydroxymethyl)-6-methylbiphenyl-3-yl)cyclopropanecarboxamide
Выход 59.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cl
Reaction #175162
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC1CCCN1CCc1cc2cc(-c3ccc(CO)cc3)ccc2o1
Reaction #176607
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
OCc1ccc(-c2cccc(Br)c2)cc1
Reaction #182659
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cl
Reaction #184031
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C1NC(=O)c2c1c(-c1ccc(CO)cc1)cc1[nH]c3ccc(O)cc3c21
Reaction #185113
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=O)c1nc(N2CCc3cccc(C(=O)N(COCC[Si](C)(C)C)c4nc5ccccc5s4)c3C2)sc1-c1ccc(CO)cc1
Reaction #192090
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Nc1ncccc1-c1nc2cc(-c3ccc(CO)cc3)cnc2n1-c1ccc(CNC(=O)c2ccccc2)cc1
Reaction #209740
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC(=O)C(NS(=O)(=O)c1ccc(-c2ccc(CO)cc2)cc1)C(C)C
Reaction #220586
2-(4′-Hydroxymethyl-biphenyl-4-sulfonylamino)-3-methyl-butyric acid methyl ester
Выход 67.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
CC1CN(c2nnc(-c3ccc(CO)cc3)c3ccncc23)CCN1C(=O)N1CCCCC1
Reaction #221618
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cl
Reaction #229606
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(C)OC(=O)N1CCC(COc2ccc(-c3ccc(CO)cc3)cc2)CC1
Reaction #237493
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cl
Reaction #243408
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cc1ccc(NC(=O)C2(c3ccc4c(c3)OCO4)CC2)cc1-c1ccc(CO)cc1
Reaction #245667
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCOC(=O)c1coc(-c2ccc(CO)cc2)n1
Reaction #247333
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
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