m-anisoyl chloride

COc1cccc(C(=O)Nc2ccccc2OC)c1
Reaction #2511
title compound
المردود 100.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1cccc(C(=O)Nc2ccccn2)c1
Reaction #2515
title compound
المردود 21.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1cccc(C(=O)NC(C)(C)c2ccccc2)c1
Reaction #49352
3-methoxy-N-(1-methyl-1-phenylethyl)benzamide
المردود 98.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
—
Reaction #56970
solid
المردود 49.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
COc1cccc(C(=O)c2ccc(OC)cc2C(=O)O)c1
Reaction #58215
5-methoxy-2-(3-methoxybenzoyl)benzoic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
COc1cccc(C(=O)Nc2nc(C)c(C(=O)NCc3ccccc3)s2)c1
Reaction #73636
title compound
المردود 34.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
COc1cccc(C(=O)N2CCC(CCO)CC2)c1
Reaction #82828
2-[1-(3-methoxybenzoyl)piperidin-4-yl]ethanol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
COc1cccc(C(=O)NC2CCN(Cc3ccc4c(c3)NC(=O)CC4)CC2)c1
Reaction #175192
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1cccc(C(=O)Nc2nc3cccc(-c4ccoc4)n3n2)c1
Reaction #175495
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1ccc(-c2[nH]nc(C)c2NC(=O)c2cccc(OC)c2)cc1
Reaction #177740
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1cccc(C(=O)N(Cc2ccc3ccc(C#N)cc3c2)c2ccc(OC3CCN(C(=O)OC(C)(C)C)CC3)cc2)c1
Reaction #179936
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1cccc(C(=O)N2CCC(N3N=C(c4ccc(OC)c(OC)c4)C(C)(C)C3=O)CC2)c1
Reaction #181206
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1cccc(C(=O)N2c3cc(Br)ccc3-n3cccc3C2C(C)(C)C)c1
Reaction #182358
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1cccc(C(=O)Nc2ccccc2)c1
Reaction #182746
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1cccc(C(=O)Nc2cc(Cl)ccc2-c2nnn[nH]2)c1
Reaction #183351
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1cccc(C(=O)OC2CCN(Cc3ccccc3)CC2)c1
Reaction #191442
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1cccc(C(=O)Nc2ccc(O)nc2)c1
Reaction #202507
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCCc1oc2ccccc2c1C(=O)c1cccc(OC)c1
Reaction #202589
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1cccc(C(=O)Nc2ccc(F)c([N+](=O)[O-])c2)c1
Reaction #209704
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1cccc(C(=O)Nc2c(C)n[nH]c2-c2ccc(OC)c(OC)c2)c1
Reaction #212220
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
الصفحة 1التالي