3,4,5-trimethoxy-iodo-benzene

COc1cc(Sc2cccc(-c3ccccc3)c2)cc(OC)c1OC
Reaction #91489
Biphenyl-3-yl(3,4,5-trimethoxyphenyl)sulfane
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
COc1cc(Sc2cccc(-c3ccccc3)c2)cc(OC)c1OC
Reaction #157220
Biphenyl-3-yl(3,4,5-trimethoxyphenyl)sulfane
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
COc1cc([SiH](C)C)c2c(C(=O)c3cc(OC)c(OC)c(OC)c3)c(C(C)(C)C)oc2c1
Reaction #280694
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COc1ccc2c(C(=O)c3cc(OC)c(OC)c(OC)c3)c([Si](C)(C)C(C)(C)C)oc2c1
Reaction #306004
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
COc1cc(C(=O)c2c(C)[nH]c3c(OC(C)C)c(OC)ccc23)cc(OC)c1OC
Reaction #306034
title compound
Выход 64.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
COc1cc(C(=O)c2c(C)oc3c(OC(C)C)c(OC)ccc23)cc(OC)c1OC
Reaction #306040
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
COc1ccc2c(C(=O)c3cc(OC)c(OC)c(OC)c3)c(C)[nH]c2c1
Reaction #306042
title compound
Выход 55.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
COc1cc(C2CC=CO2)cc(OC)c1OC
Reaction #339953
title compound 287
Выход 43.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_01
COc1cc(C2CC=CO2)cc(OC)c1OC
Reaction #371962
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
COc1cc(C(=O)c2c(-c3cnn(Cc4ccccc4)c3)oc3c(O)c(OC)ccc23)cc(OC)c1OC
Reaction #393218
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
COc1cc(I)cc(OC)c1O
Reaction #482628
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_08
COc1cc(C(O)c2cc(OC)c(OC)c(OC)c2)c([N+](=O)[O-])cc1OC
Reaction #503448
title compound 241
Выход 40.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_01
COc1cc(Sc2cccc(-c3ccccc3)c2)cc(OC)c1OC
Reaction #609749
Biphenyl-3-yl(3,4,5-trimethoxyphenyl)sulfane
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_05
COc1ccc2c(C(=O)c3cc(OC)c(OC)c(OC)c3)c([Si](C)(C)C(C)(C)C)oc2c1
Reaction #616415
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_05
COc1cc(C(=O)c2c(C)[nH]c3c(OC(C)C)c(OC)ccc23)cc(OC)c1OC
Reaction #616445
title compound
Выход 64.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_05
COc1cc(C(=O)c2c(C)oc3c(OC(C)C)c(OC)ccc23)cc(OC)c1OC
Reaction #616451
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_05
COc1ccc2c(C(=O)c3cc(OC)c(OC)c(OC)c3)c(C)[nH]c2c1
Reaction #616453
title compound
Выход 55.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_05
COc1cc(Nc2ccc3c(c2)OCO3)cc(OC)c1OC
Reaction #775391
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
COc1cc(C2CC=CO2)cc(OC)c1OC
Reaction #823680
title compound 287
Выход 43.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_09
COc1cc(C(O)c2cc(OC)c(OC)c(OC)c2)c([N+](=O)[O-])cc1OC
Reaction #908726
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
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