2-naphthaleneboronic acid

COc1cc(C=C2C(=O)Nc3ccccc32)c(-c2ccc3ccccc3c2)cc1OC
Reaction #52692
3-(4,5-dimethoxy-2-naphthalen-2-ylbenzylidene)-1,3-dihydroindol-2-one
Выход 30.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CS(=O)(=O)c1ccccc1S(=O)(=O)Nc1ccc2[nH]nc(-c3cccc4ccccc34)c2c1
Reaction #53704
2-methylsulfonyl-N-(3-naphthalen-1-yl-1H-indazol-5-yl)benzenesulfonamide
Выход 58.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CS(=O)(=O)c1ccccc1S(=O)(=O)Nc1ccc2[nH]nc(-c3ccc4ccccc4c3)c2c1
Reaction #53705
2-methylsulfonyl-N-(3-naphthalen-2-yl-1H-indazol-5-yl)benzenesulfonamide
Выход 29.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
c1ccc(C(c2ccccc2)(c2ccccc2)n2nc(-c3ccc4ccccc4c3)c3ncccc32)cc1
Reaction #62339
title compound
Выход 28.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
N#Cc1c(Cl)cncc1-c1ccc2ccccc2c1
Reaction #168208
3-chloro-5-(naphthalen-2-yl)isonicotinonitrile
Выход 52.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cc1ccc(S(=O)(=O)OCC2Cc3cccc(-c4ccc5ccccc5c4)c3O2)cc1
Reaction #234626
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCOC(=O)c1ccnc(-c2ccc3ccccc3c2)c1
Reaction #252981
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cn1cc(-c2ccc3ccccc3c2)c2c(Cl)ncnc21
Reaction #325211
ZK102
Выход 26.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
Nc1cccc(-c2ccc3ccccc3c2)c1
Reaction #327281
3-Naphthalen-2-yl-phenylamine
Выход 63.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
c1ccc([Si](c2ccccc2)(c2ccccc2)c2c3ccccc3c(-c3ccc4ccccc4c3)c3ccccc23)cc1
Reaction #357918
Compound 2
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_11
CN1CCC(c2c[nH]c3ccc(-c4ccc5ccccc5c4)nc23)CC1
Reaction #365187
title compound
Выход 91.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_03
CCOC(=O)c1cc(C)nn1-c1ccc2ccccc2c1
Reaction #376970
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
COc1ccc(-c2ccc3ccccc3c2)c(OC)c1-c1ccccn1
Reaction #412124
39
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_04
COC(=O)c1ccc(I)c(Oc2ccc3ccccc3c2)c1
Reaction #466220
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_10
CC1CC(c2ccc3ccccc3c2)=CCN1C(=O)Oc1ccccc1
Reaction #467732
title compound
Выход 50.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_10
CCC1CC(c2ccc3ccccc3c2)=CCN1C(=O)Oc1ccccc1
Reaction #467733
desired compound
Выход 75.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_10
COC(=O)c1cn(-c2ccc3ccccc3c2)cn1
Reaction #485101
title compound
Выход 24.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_08
CN1Cc2ccccc2C(c2ccc3ccccc3c2)C1
Reaction #489283
desired product
Выход 447.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_06
Oc1ccc(-c2ccc3ccccc3c2)nc1
Reaction #506051
6-naphthalen-2-yl-pyridin-3-ol
Выход 17.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_01
CCOC(=O)Cc1c(C(=O)OCC)c2cc(Oc3ccc4ccccc4c3)ccc2n1-c1ccc(N(CC)CC)cc1
Reaction #508164
sub-title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_01
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