naphthalene

O=C(O)CCC(=O)c1cccc2ccccc12
Reaction #1597
3(1-naphthoyl)propionic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(O)CCC(=O)c1cccc2ccccc12
Reaction #1664
3-(1-naphthoyl)propionic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(O)CCC(=O)c1cccc2ccccc12
Reaction #2169
3-(1-naphthoyl)propionic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(O)CCC(=O)c1cccc2ccccc12
Reaction #2210
3-(1-naphthoyl)propionic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1cc(I)cc2ccccc12
Reaction #5390
3-iodo-1-methoxynaphthalene
Ausbeute 18.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CC(C)Cc1ccc(C(C)C(=O)O)cc1
Reaction #6618
(+) ibuprofen
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
[Na].c1ccc2ccccc2c1
Reaction #8649
Sodium naphthalene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Cc1cc(C)c(C(=O)P(=O)(c2ccccc2)c2ccccc2)c(C)c1
Reaction #11028
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
[Na].c1ccc2ccccc2c1
Reaction #11286
Sodium naphthalene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
c1ccc2ccccc2c1
Reaction #50909
naphthalene
Ausbeute 142.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
—
Reaction #52640
ethyl acetate hexanes
Ausbeute 40.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
O=C1c2ccccc2C(=O)c2ccccc21
Reaction #55330
anthraquinone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09
CC1(C)OB(c2cnn(Cc3ccc4ccccc4c3)c2)OC1(C)C
Reaction #69210
1-(2-naphthylmethyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CC1(C)OB(c2cnn(Cc3ccc4ccccc4c3)c2)OC1(C)C
Reaction #73244
1-(2-naphthylmethyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
C1CCOC1.[Na].c1ccc2ccccc2c1
Reaction #158230
Sodium Naphthalene Tetrahydrofuran
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCCCCCCC(=O)Oc1cccc2ccccc12
Reaction #190215
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)C(=O)c1cccc2ccccc12
Reaction #192450
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1cc(C)c(C(=O)P(=O)(c2ccccc2)c2ccccc2)c(C)c1
Reaction #200005
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(CCCCl)c1ccc2ccccc2c1
Reaction #223083
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=[N+]([O-])c1cccc2ccccc12
Reaction #228802
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
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