methyl-4-bromobenzoate

COC(=O)c1ccc(NCc2cc(F)cc(F)c2)cc1
Reaction #578
収率 0.0%750 AstraZeneca ELN dataset
COC(=O)c1ccc(NCc2cc(F)cc(F)c2)cc1
Reaction #579
収率 0.0%750 AstraZeneca ELN dataset
COC(=O)c1ccc(N2CCc3ccccc3C2)cc1
Reaction #580
収率 0.0%750 AstraZeneca ELN dataset
COC(=O)c1ccc(-c2ncco2)cc1
Reaction #9066
methyl-4-(oxazol-2-yl)-benzoate
収率 42.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COC(=O)c1ccc(N2CCN(C(C)C)CC2)cc1
Reaction #45055
methyl 4-(4-propan-2-yl-piperizin-1-yl)benzoate
収率 64.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COC(=O)c1ccc(N2CCN(C(C)=O)CC2)cc1
Reaction #45063
methyl 4-(4-acetylpiperazin-1-yl)benzoate
収率 56.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COC(=O)c1ccc(-c2ccccc2-c2nnn(C(C)(C)c3ccccc3)n2)cc1
Reaction #64302
2'-[2-(1-methyl-1-phenylethyl)-2H-tetrazol-5-yl]biphenyl-4-carboxylic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
COC(=O)c1ccc(-c2ccccc2-c2nnn(C(C)(C)c3ccccc3)n2)cc1
Reaction #64315
2'-[2-(1-methyl-1-phenylethyl)-2H-tetrazol-5-yl]biphenyl-4-carboxylic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
COC(=O)c1ccc(N2CCN(c3cnccc3C)C2=O)cc1
Reaction #167250
4-[3-(4-Methyl-pyridin-3-yl)-2-oxo-imidazolidin-1-yl]-benzoic acid methyl ester
収率 91.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
COC(=O)c1ccccc1
Reaction #172193
methyl benzoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
COC(=O)c1ccc(C(=CC2CCCCC2)CO)cc1
Reaction #179131
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(O)c1ccc(Br)cc1
Reaction #192049
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC(=O)c1ccc(NCCOC(C)C)cc1
Reaction #199521
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC(=O)c1ccc(-c2ccc(F)cc2)cc1
Reaction #226265
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCCCc1ccc(C#Cc2ccc(C(=O)OC)cc2)cc1
Reaction #244451
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COC(=O)c1ccc(Oc2cc3c(cc2C)C(C)(C)CCC3(C)C)cc1
Reaction #245924
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COC(=O)c1ccc(-c2ccc3cc(OCc4ccccc4)c(C45CC6CC(CC(C6)C4)C5)cc3c2)cc1
Reaction #247384
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COC(=O)c1ccc(Oc2ccc(CN(Cc3ccc(F)cc3F)c3cccc([N+](=O)[O-])c3C)cc2)cc1
Reaction #257917
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COC(=O)c1ccc(-c2ccccc2Cl)cc1
Reaction #286564
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COC(=O)c1ccc(-c2cnc(C(=O)CCCCCCc3ccccc3)o2)cc1
Reaction #299382
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
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