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256743

COc1cc(N2CCN(C(=O)OC(C)(C)C)CC2=O)ccc1[N+](=O)[O-]
Reaction #279
Выход 68.4%
COc1cc(N2CCN(C(=O)OC(C)(C)C)CC2=O)ccc1[N+](=O)[O-]
Reaction #280
Выход 100.3%
Cc1cccc(N2CCN(C(=O)OC(C)(C)C)CC2)c1[N+](=O)[O-]
Reaction #314
Выход 16.8%
—
Reaction #4533
liquid
DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCC(N2C(=O)c3cccc(CNC(=O)NC4CC4)c3C2=O)C(=O)N1
Reaction #10123
N-{[2-(2,6-dioxo(3-piperidyl))-1,3-dioxoisoindolin-4-yl]methyl}(cyclopropylamino)carboxamide
Выход 77.4%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(OC2CCN(C(=O)OC(C)(C)C)CC2)ccc1[N+](=O)[O-]
Reaction #48168
4-(3-Methyl-4-nitro-phenoxy)-piperidine-1-carboxylic acid tert-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(=O)Cc1cc(OC2CCN(C(=O)OC(C)(C)C)CC2)ccc1[N+](=O)[O-]
Reaction #48169
4-[3-(2-Ethoxycarbonyl-2-oxo-ethyl)-4-nitro-phenoxy]-piperidine-1-carboxylic acid tert-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCN(c2c(Cl)cccc2[N+](=O)[O-])CC1
Reaction #61869
4-(2-chloro-6-nitro-phenyl)-piperazine-1-carboxylic acid tert-butyl ester
Выход 70.2%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)OC1CCN(C(=O)OCc2ccc([N+](=O)[O-])cc2)C1
Reaction #65554
4-methanesulfonyloxy-1-(4-nitrobenzyloxycarbonyl)pyrrolidine
Выход 124.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CC=C(c2ccc(N)c([N+](=O)[O-])c2)CC1
Reaction #86418
title compound
Выход 75.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(C2=CCN(C(=O)OC(C)(C)C)CC2)ccc1[N+](=O)[O-]
Reaction #88645
4-(3-methoxy-4-nitro-phenyl)-3,6-dihydro-2H-pyridine-1-carboxylic acid tert-butyl ester
Выход 90.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(N2CCN(C(=O)OC(C)(C)C)CC2)c([N+](=O)[O-])c1
Reaction #157029
tert-butyl 4-(4-methoxy-2-nitro phenyl)piperazine-1-carboxylate
Выход 50.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCN(c2c(F)cc(N)cc2F)CC1
Reaction #164610
title compound
Выход 95.0%DOI: 10.6084/m9.figshare.5104873.v1
NC(=NOC(=O)c1ccccc1)c1nc(Br)cnc1N
Reaction #165751
product
Выход 70.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ncc(Br)nc1-c1noc(-c2ccccc2)n1
Reaction #165752
resultant product
Выход 87.0%DOI: 10.6084/m9.figshare.5104873.v1
N=C(NOC(=O)c1ccccc1)c1nc(Br)cnc1N
Reaction #165778
desired product
Выход 69.1%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ncc(Br)nc1-c1noc(-c2ccccc2)n1
Reaction #165779
5-bromo-3-(5-phenyl-1,2,4-oxadiazol-3-yl)pyrazin-2-amine
Выход 76.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)c1cccc(Oc2ccc([N+](=O)[O-])c(N(C)C(=O)OC(C)(C)C)c2)c1
Reaction #174061
DOI: 10.1039/C8SC04228D
Cc1cc(OC2CCN(C(=O)OC(C)(C)C)CC2)ccc1N
Reaction #176740
DOI: 10.1039/C8SC04228D
CN(CC1(C)Cn2cc([N+](=O)[O-])nc2O1)C(=O)OCc1ccc(F)cc1
Reaction #178175
DOI: 10.1039/C8SC04228D
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