3-benzyloxyphenol

Oc1cccc(OCc2ccccc2)c1C[C@H]1CO1
Reaction #1615
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOC(=O)CCC(Oc1cccc(OCc2ccccc2)c1)c1ccccc1
Reaction #189075
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
N#Cc1ccc(Oc2cccc(OCc3ccccc3)c2)s1
Reaction #251267
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cn1nc(COc2cccc(OCc3ccccc3)c2)c2c(Cl)ncnc21
Reaction #285051
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
O=C1N(C(c2ccccc2)c2ccccc2)c2ccccc2C1(O)c1ccc(OCc2ccccc2)cc1O
Reaction #383178
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CCNC(=O)c1ccc(OCc2ccccc2)cc1OC(CCC(=O)OCC)c1ccccc1
Reaction #406732
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CCOC(=O)CCC(Oc1cccc(OCc2ccccc2)c1)c1ccccc1
Reaction #410058
ethyl (RS)-4-(3-benzyloxyphenoxy)-4-phenylbutanoate
Ausbeute 17.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_04
CCNC(=O)c1ccc(OCc2ccccc2)cc1OC(CCC(=O)OCC)c1ccccc1
Reaction #410060
ethyl (RS)-4-[2-(N-ethylcarbamoyl)-5-benzyloxyphenoxy]-4-phenyl-butanoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_04
O=S(=O)(Oc1cccc(OCc2ccccc2)c1)c1ccccc1Cl
Reaction #455725
title compound
Ausbeute 95.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_10
c1ccc(COc2cccc(OCC3CCC4(CC3)OCCO4)c2)cc1
Reaction #471643
8-{[3-(benzyloxy)phenoxy]methyl}-1,4-dioxaspiro[4.5]decane
Ausbeute 47.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_02
CC(C)(C)[Si](C)(C)Oc1cccc(OCc2ccccc2)c1
Reaction #493185
(3-Benzyloxy-phenoxy)-tert-butyl-dimethyl-silane
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_06
O=[N+]([O-])c1cc(Cl)ccc1-c1cccc(OCc2ccccc2)c1
Reaction #499313
titled product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_05
O=C1N(C(c2ccccc2)c2ccccc2)c2ccccc2C1(O)c1ccc(OCc2ccccc2)cc1O
Reaction #510018
3-[4-(benzyloxy)-2-hydroxyphenyl]-1-(diphenylmethyl)-3-hydroxy-1,3-dihydro-2H-indol-2-one
Ausbeute 97.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_01
Cn1c(C(F)(F)F)cc(=O)n(-c2cc(Oc3cccc(OCc4ccccc4)c3)c([N+](=O)[O-])cc2F)c1=O
Reaction #520890
2-(3-benzyloxyphenoxy)-5-fluoro-4-[3-methyl-2,6-dioxo-4-(trifluoromethyl)-1,2,3,6-tetrahydropyrimidin-1-yl]nitrobenzene
Ausbeute 52.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_12
O=S(=O)(Oc1cccc(OCc2ccccc2)c1)c1ccccc1Cl
Reaction #569261
title compound
Ausbeute 95.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_08
CN(C)CCOc1cccc(OCc2ccccc2)c1
Reaction #660234
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_05
c1ccc(COc2ccc(OCCN3CCOCC3)cc2)cc1
Reaction #660250
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_05
CN(C)C(=O)COc1ccc(OCc2ccccc2)cc1
Reaction #660251
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_05
CN(C)CCOc1cccc(OCc2ccccc2)c1
Reaction #711522
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_04
c1ccc(COc2ccc(OCCN3CCOCC3)cc2)cc1
Reaction #711537
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_04
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