Impliqué dans 188 réactions

4587

CC(=O)c1cc[n+]([O-])cc1
Reaction #2249
4-acetyl-pyridine N-oxide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Br.O=C(CBr)c1ccncc1
Reaction #4440
α-Bromo-4-acetylpyridine hydrobromide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
CC(=CC(=O)OCc1ccccc1)c1ccncc1
Reaction #11543
benzyl 3-(4-pyridyl)-2-butenoate
Rendement 42.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC(=CC(=O)OCc1ccccc1)c1ccncc1
Reaction #46668
benzyl 3-(4-pyridyl)-2-butenate
Rendement 42.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(C)(C)OC(=O)N1CCC(CC(=O)CC(=O)c2ccncc2)CC1
Reaction #179909
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(O)c1ccncc1
Reaction #187036
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(=NNc1ccc(I)cc1)c1ccncc1
Reaction #195269
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(c1ccccc1Cl)c1cccnc1C=C(O)c1ccncc1
Reaction #217864
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
O=C(c1ccccc1Cl)c1cccnc1C=C(O)c1ccncc1.O=P(O)(O)O
Reaction #217865
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
CC(O)c1ccncc1
Reaction #259262
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=C(CBr)c1ccncc1
Reaction #265119
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CC(c1ccncc1)N1CCC(CNc2ccccc2C(=O)Nc2ccc(Cl)cn2)CC1
Reaction #269482
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CC(=O)NN=C(C)c1ccncc1
Reaction #280763
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CC(C)(C)OC(=O)N1CCC(CCC(=O)CC(=O)c2ccncc2)CC1
Reaction #308534
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
CC(C)(C)OC(=O)N1CCC(OCC(=O)CC(=O)c2ccncc2)CC1
Reaction #308535
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
CC(C)(C)OC(=O)N1CCC(CC(=O)CC(=O)c2ccncc2)CC1
Reaction #308536
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
—
Reaction #319211
crude product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1989_07
CC(C)(O)c1ccncc1
Reaction #321827
title compound
Rendement 45.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_01
O=c1nc(-c2ccncc2)cc[nH]1
Reaction #485217
4-(4-Pyridyl)-2(1H)-pyrimidinone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_08
C[C@@H](O)c1ccncc1
Reaction #510815
(1R)-1-(4-pyridinyl)ethanol
Rendement 55.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_01
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