#1193

COc1ccc(N2CCN(C(C)=O)CC2)cc1[N+](=O)[O-]
Reaction #142
収率 29.9%750 AstraZeneca ELN dataset
COc1ccc(N2CCN(C(C)=O)CC2)cc1[N+](=O)[O-]
Reaction #143
収率 82.9%750 AstraZeneca ELN dataset
COc1ccc(N2CCN(C(C)=O)CC2)cc1[N+](=O)[O-]
Reaction #144
収率 1.2%750 AstraZeneca ELN dataset
COc1ccc(N2CCN(C(C)=O)CC2)cc1[N+](=O)[O-]
Reaction #145
収率 1.4%750 AstraZeneca ELN dataset
COc1ccc(N2CC3CN(C(C)=O)CC(C2)O3)cc1[N+](=O)[O-]
Reaction #182
収率 0.0%750 AstraZeneca ELN dataset
COc1ccc(N2CC3CN(C(C)=O)CC(C2)O3)cc1[N+](=O)[O-]
Reaction #188
収率 0.0%750 AstraZeneca ELN dataset
COc1ccc(N2CCN(C(C)=O)CC2)cc1[N+](=O)[O-]
Reaction #287
収率 77.5%750 AstraZeneca ELN dataset
COc1ccc(N2CCN(C(C)=O)CC2)cc1[N+](=O)[O-]
Reaction #288
収率 85.8%750 AstraZeneca ELN dataset
COc1ccc(N2C[C@@H](C)N[C@@H](C)C2)cc1[N+](=O)[O-]
Reaction #321
収率 56.0%750 AstraZeneca ELN dataset
COc1ccc(N2C[C@@H](C)N[C@@H](C)C2)cc1[N+](=O)[O-]
Reaction #322
収率 89.8%750 AstraZeneca ELN dataset
COc1ccc(N2C[C@@H]3C[C@H]2CO3)cc1[N+](=O)[O-]
Reaction #80127
(1S,4S)-5-(4-methoxy-3-nitro-phenyl)-2-oxa-5-aza-bicyclo[2.2.1]heptane
収率 66.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
COc1ccc(N(C)CC2CCOCC2)cc1[N+](=O)[O-]
Reaction #80166
(4-methoxy-3-nitro-phenyl)-methyl-(tetrahydro-pyran-4-ylmethyl)-amine
収率 62.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
COc1ccc(N(C)C2CCOCC2)cc1[N+](=O)[O-]
Reaction #80174
(4-methoxy-3-nitro-phenyl)-methyl-(tetrahydro-pyran-4-yl)-amine
収率 18.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
COc1ccc(N2CC(C)NC(C)C2)cc1[N+](=O)[O-]
Reaction #191527
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1ccc(N2C[C@@H](C)N[C@@H](C)C2)cc1[N+](=O)[O-]
Reaction #217581
title product ( D3 )
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
COc1ccc(Br)cc1N
Reaction #225089
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COc1ccc(N(C)CC2CCOCC2)cc1[N+](=O)[O-]
Reaction #254476
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COc1ccc(N2CCC(OC)CC2)c2sc(NC(=O)N3CCOCC3)nc12
Reaction #280257
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COc1ccc(C2=CCCCC2)cc1[N+](=O)[O-]
Reaction #280724
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COc1ccc(Br)cc1N
Reaction #338683
5-bromo-2-methoxyaniline
収率 76.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_01
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