3-phenoxybenzyl alcohol

O=Cc1cccc(Oc2ccccc2)c1
Reaction #976
aldehyde
Rendement 90.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=Cc1cccc(Oc2ccccc2)c1
Reaction #81839
aldehyde
Rendement 90.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
ClCc1cccc(Oc2ccccc2)c1
Reaction #165056
title compound
Rendement 94.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
BrCc1cccc(Oc2ccccc2)c1
Reaction #177012
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
OCc1cccc(Oc2ccccc2)c1
Reaction #190855
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)C(C=Cc1cccc(F)c1)C(=O)OCc1cccc(Oc2ccccc2)c1
Reaction #194233
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
OCc1cc(Oc2ccccc2)ccc1Br
Reaction #198453
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)C(Nc1ccc(Cl)cc1)C(=N)OCc1cccc(Oc2ccccc2)c1
Reaction #214162
3-phenoxybenzyl 2-(4-chlorophenylamino)-3-methylbutanimidate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1981_03
CC(C)C(C(=N)OCc1cccc(Oc2ccccc2)c1)c1ccc(Cl)cc1
Reaction #214165
3-phenoxybenzyl 2-(4-chlorophenyl)-3-methylbutanimidate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1981_03
OCc1cccc(Oc2ccccc2)c1
Reaction #244219
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC1(C)C(Oc2ccc(Cl)cc2)C1C(=O)OCc1cccc(Oc2ccccc2)c1
Reaction #244242
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
ClCc1cccc(Oc2ccccc2)c1
Reaction #284823
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
O=Cc1cccc(Oc2ccccc2)c1
Reaction #287128
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CC1(C)C(C=C(Cl)C(F)(F)F)C1C(=O)OCc1cccc(Oc2ccccc2)c1
Reaction #294811
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
O=C(OCc1cccc(Oc2ccccc2)c1)C12CC3CC(CC(C3)C1)C2
Reaction #301899
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
OCc1cccc(Oc2ccccc2)c1
Reaction #334906
3-phenoxybenzyl alcohol
Rendement 95.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1987_11
OCc1cccc(Oc2ccccc2)c1
Reaction #334907
3-phenoxybenzyl alcohol
Rendement 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1987_11
OCc1cccc(Oc2ccccc2)c1
Reaction #334908
3-phenoxybenzyl alcohol
Rendement 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1987_11
OCc1cccc(Oc2ccccc2)c1
Reaction #368879
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CCOC(=O)C(F)=CC1C(C(=O)OCc2cccc(Oc3ccccc3)c2)C1(C)C
Reaction #380548
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
Page 1Suivant