2,4-dimethoxy benzaldehyde

COc1ccc(CNc2ccc(Cl)cc2C(O)c2ccccc2Cl)c(OC)c1
Reaction #1868
5-chloro-α-(2-chlorophenyl)-2-(2,4-dimethoxybenzyl)aminobenzyl alcohol
収率 96.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1ccc(C(CC(=O)c2ccco2)CC(=O)c2ccco2)c(OC)c1
Reaction #5645
1,5-Di(2-furyl)-3-(2,4-dimethoxyphenyl)-1,5-pentanedione
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
COc1ccc(-c2nc3ccccc3[nH]2)c(OC)c1
Reaction #10787
2-(2,4-dimethoxy-phenyl)-1H-benzoimidazole
収率 12.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COc1cc(OC)c(C=O)cc1I
Reaction #10849
title compound
収率 87.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COc1ccc(CNc2ncns2)c(OC)c1.COc1ccc(CNc2ncns2)c(OC)c1
Reaction #74555
title compound
収率 49.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
COc1ccc(CNc2ncc(Cl)s2)c(OC)c1
Reaction #74575
title compound
収率 32.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
COc1ccc(CNc2nncs2)c(OC)c1
Reaction #74595
title compound
収率 45.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
COc1ccc(CNc2nncs2)c(OC)c1
Reaction #74596
title compound
収率 73.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
COc1ccc(CNCC(=O)O)c(OC)c1
Reaction #95584
N-(2,4-dimethoxybenzyl)glycine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_08
COc1ccc(CNCC(=O)O)c(OC)c1
Reaction #95635
N-(2,4-dimethoxybenzyl)glycine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_08
COc1ccc(CNCC(=O)O)c(OC)c1
Reaction #95683
N-(2,4-dimethoxybenzyl)glycine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_08
COc1ccc(CNCC(=O)O)c(OC)c1
Reaction #95732
N-(2,4-dimethoxybenzyl)glycine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_08
COc1ccc(CNCC(=O)O)c(OC)c1
Reaction #95780
N-(2,4-dimethoxybenzyl)glycine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_08
COc1ccc(CNCC(=O)O)c(OC)c1
Reaction #95832
N-(2,4-dimethoxybenzyl)glycine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_08
COc1ccc(CNCC(=O)O)c(OC)c1
Reaction #95881
N-(2,4-dimethoxybenzyl)glycine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_08
CC(C)(C)OC(=O)NC[C@@H](C(=O)O)c1ccc(Cl)cc1
Reaction #169569
(S)-3-(tert-butoxycarbonylamino)-2-(4-chlorophenyl)propanoic acid
収率 94.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
COc1ccc(CNc2nccs2)c(OC)c1
Reaction #207968
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1ccc(C=C2Oc3cc(O)ccc3C2=O)c(OC)c1
Reaction #236556
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COc1ccc(C=C[N+](=O)[O-])c(OC)c1
Reaction #246257
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
C#CCNCc1ccc(OC)cc1OC
Reaction #249972
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
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