1-methyl-3,4-dihydroisoquinoline

CC(C)(C)N1CCC(Cl)CC1
Reaction #87988
1-tert-butyl-4-chloropiperidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CC1=NCCc2ccc([N+](=O)[O-])cc21
Reaction #237791
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC1=NCCc2ccc([N+](=O)[O-])cc21
Reaction #403920
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CC1=NCCc2ccc([N+](=O)[O-])cc21
Reaction #457164
1-Methyl-7-nitro-3,4-dihydroisoquinoline
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_10
CC1=NCCc2ccc([N+](=O)[O-])cc21
Reaction #568962
1-methyl-7-nitro-3,4-dihydroisoquinoline
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_08
CC1=NCCc2ccc([N+](=O)[O-])cc21
Reaction #670465
1-Methyl-7-nitro-3,4-dihydroisoquinoline
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_07
CC1=NCCc2ccc([N+](=O)[O-])cc21
Reaction #738132
title compound
Rendement 57.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_08
CC1=NCCc2ccccc21
Reaction #932123
1-methyl-3,4-dihyroisoquinoline
Rendement 79.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_07
CC1NCCc2ccccc21
Reaction #932124
1-methyl-1,2,3,4-tetrahydroisoquinoline
Rendement 96.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_07
C[C@H]1NCCc2ccccc21
Reaction #1102170
(R)-1-Methyl-1,2,3,4-tetrahydroisoquinoline
Rendement 82.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_07
CC1=NCCc2ccccc21
Reaction #1102214
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_07
CC1NCCc2ccccc21
Reaction #1102234
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_07
CC1NCCc2ccccc21
Reaction #1204554
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (7/10)
CC1=[N+](C)CCc2ccccc21
Reaction #1327596
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (5/10)
CC1=NCCc2ccccc21
Reaction #1352072
titled compound
Rendement 97.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_04
CC1NCCc2ccccc21
Reaction #1352073
titled compound
Rendement 93.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_04
CC1=NCCc2ccccc21
Reaction #2380305
title compound
Rendement 86.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_11
CC1NCCc2ccccc21
Reaction #2380306
title compound
Rendement 93.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_11
CC1=[N+](C)CCc2ccccc21.[I-]
Reaction #2384790
crystals
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_12
CC1NCCc2ccccc21
Reaction #2407332
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (10/10)