2-hydroxyacetophenone

O=C1CCOc2ccccc21
Reaction #801772
chroman-4-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_11
CC(=O)c1ccc(OCc2ccc(CN3CCCCC3)cc2)cc1
Reaction #809862
α-(4-Acetylphenoxy)-α′-piperidino p-xylol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_11
CC(=O)c1ccc(OCc2ccc(CN3CCCC3)cc2)cc1
Reaction #809863
α-(4-Acetylphenoxy)-α′-(1-pyrrolidinyl)p-xylol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_11
COc1cc(C(=O)Oc2ccccc2C(C)=O)cc([N+](=O)[O-])c1OC
Reaction #812569
o-acetylphenyl 3,4-dimethoxy-5-nitrobenzoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_01
C=Cc1ccc(-c2oc3ccccc3c(=O)c2O)cc1
Reaction #829261
4'-vinyl-3-hydroxyflavone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_09
O=c1c(O)c(-c2ccccc2)oc2ccccc12
Reaction #829262
3-hydroxyflavone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_09
O=c1cc(-c2sccc2O)oc2ccccc12
Reaction #829263
chalcone
Выход 46.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_09
O=c1cc(C2(O)C=CSC2)oc2ccccc12
Reaction #829264
chalcone
Выход 36.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_09
CC=Cc1ccc(-c2oc3ccccc3c(=O)c2O)cc1
Reaction #829265
4'-(β-Methylethenyl)-3-hydroxyflavone
Выход 35.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_09
O=C(C=Cc1ccccc1)c1ccccc1
Reaction #829266
chalcone
Выход 33.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_09
OCC(O)c1ccccc1
Reaction #906549
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
O=C(CC(O)c1ccncc1)c1ccccc1O
Reaction #935343
1-(2-hydroxyphenyl) 3-(4-pyridyl) 3-hydroxy 1-propanone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1981_10
Nc1ccc(C(=O)C=Cc2ccncc2)cc1
Reaction #935344
1-(4-aminophenyl) 3-(4-pyridyl) 2-propene-1-one
Выход 98.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1981_10
O=C1CCOc2ccccc21
Reaction #949656
compound 3
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_02
COCOCC(=O)c1ccccc1
Reaction #970300
product
Выход 45.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_08
O=C1CC(c2ccccc2)(c2ccncc2)Oc2ccccc21
Reaction #1046148
DOI: 10.1039/C8SC04228DValidation data from https://doi.org/10.1039/C8SC04228D
CC1(C)CC(=O)c2cc3c(cc2O1)C(C)(C)CCC3(C)C
Reaction #1051677
2,3,6,7,8,9-hexahydro-2,2,6,6,9,9-hexamethylbenzo [g]chromen-4-one
Выход 26.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_06
CC1(C)CC(=O)c2cc3c(cc2O1)C(C)(C)CCC3(C)C
Reaction #1051685
2,3,6,7,8,9-hexahydro-2,2,6,6,9,9-hexamethylbenzo [g]chromen-4-one
Выход 26.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_06
CC1(C)CC(=O)c2cc3c(cc2O1)C(C)(C)CCC3(C)C
Reaction #1051693
2,3,6,7,8,9-hexahydro-2,2,6,6,9,9-hexamethylbenzo [g]chromen-4-one
Выход 26.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_06
CC(=O)Oc1cccc(C)c1
Reaction #1065976
m-cresyl acetate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1987_05
НазадСтраница 3Далее