normal dodecane

CCCCCCCCCCCC
Reaction #863
dodecane
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(O)Cc1cccc(-n2cccn2)c1
Reaction #44062
title compound
収率 65.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
—
Reaction #55486
1,10-decane dicarboxylic acids
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09
c1ccc2ncccc2c1
Reaction #81070
quinoline
収率 95.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
COC(=O)c1cccc(Nc2ccc(OC)cc2)c1
Reaction #189150
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1ccc(Nc2cc(C)cc(C)c2)cc1
Reaction #191848
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1cc(C)cc(Nc2ccc(C#N)cc2)c1
Reaction #208740
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=[N+]([O-])c1ccccc1-n1ccc2ccccc21
Reaction #211906
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1cc(C)cc(N(c2ccccc2)c2ccccc2)c1
Reaction #221988
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COc1ccc(Nc2ccccc2[N+](=O)[O-])cc1
Reaction #224443
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COC(=O)c1cn(-c2ncccn2)cc1C
Reaction #229015
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCCCCCCOc1cc(C)cc(C)c1
Reaction #230189
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
c1ccc2c(c1)CCC1OC21
Reaction #237719
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cc1cc(C)cc(NN=C(c2ccccc2)c2ccccc2)c1
Reaction #251421
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cc1cc(C)cc(NC(C)c2ccccc2)c1
Reaction #252815
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCCCCCCOc1cc(C)cc(C)c1
Reaction #254545
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
c1ccc(C2CO2)cc1
Reaction #263336
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Cc1cc(C)cc(N2CCCC2=O)c1
Reaction #264113
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COC(=O)c1cn(-c2cc3ccccc3cn2)c2ccccc12
Reaction #270082
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COc1ccccc1Nc1ccccc1[N+](=O)[O-]
Reaction #272131
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
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