2-hydroxyacetophenone

COc1ccccc1C(=O)OCC(=O)c1ccccc1
Reaction #485198
compound
Выход 89.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_08
CC(=Nc1ccc(O)cc1C)c1ccccc1O
Reaction #521904
4-[1-(2-hydroxyphenyl)ethylideneamino]-3-methylphenol
Выход 840.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1983_08
COc1ccccc1CNC(=N)Nc1nc(-c2ccccc2)co1
Reaction #535125
pure product
Выход 10.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_07
COCOCC(=O)c1ccccc1
Reaction #555254
product
Выход 45.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_01
CC=CCCC1CCC=CO1
Reaction #582528
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_09
CC=CCCC1CCC=CO1
Reaction #582529
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_09
N#Cc1c(-c2ccccc2)coc1N
Reaction #589847
product
Выход 49.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_08
COCOCC(=O)c1ccccc1
Reaction #600086
product
Выход 45.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_08
CC(C)(O)c1ccccc1O
Reaction #600101
hydroxy phenol
Выход 45.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_08
OCC1(c2ccccc2)OCCO1
Reaction #635374
(2-phenyl-[1,3]dioxolan-2-yl)methanol
Выход 98.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_05
C=CCOc1ccccc1C(C)=O
Reaction #644569
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_11
CCCC(=O)Oc1ccccc1C(C)=O
Reaction #669799
2-Acetylphenyl butyrate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_07
CC(=O)c1ccc(OCc2ccc(CN3CCCCC3)cc2)cc1
Reaction #691569
α-(4-Acetylphenoxy)-α′-piperidino p-xylol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_03
CC(=O)c1ccc(OCc2ccc(CN3CCCC3)cc2)cc1
Reaction #691570
α-(4-Acetylphenoxy)-α′-(1-pyrrolidinyl) p-xylol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_03
—
Reaction #740410
hydroxy aromatic ketones
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1987_06
O=C(C=Cc1ccccc1)c1ccccc1
Reaction #760927
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
O=C(COCc1csc(-c2ccc(F)cc2)n1)c1ccccc1
Reaction #767240
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
CC1(C)CC(=O)c2ccccc2O1
Reaction #771305
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
CCOC(=O)COCC(=O)c1ccccc1
Reaction #787073
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
O=C1CCOc2ccccc21
Reaction #801771
chroman-4-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_11
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