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283200

CC1(C)C(=O)Nc2cc(N)ccc21
Reaction #47919
solid
Ausbeute 68.5%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CNc2cc([N+](=O)[O-])ccc21
Reaction #47921
3,3-dimethyl-6-nitroindoline
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N1CC(C)(C)c2ccc([N+](=O)[O-])cc21
Reaction #47922
1-(3,3-dimethyl-6-nitroindolin-1-yl)ethanone
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N1CC(C)(C)c2ccc(N)cc21
Reaction #47923
solid
Ausbeute 99.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1ccc([N+](=O)[O-])cc1N
Reaction #161148
2-tert-butyl-5-nitroaniline
Ausbeute 64.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1ccc([N+](=O)[O-])cc1O
Reaction #161149
2-tert-butyl-5-nitrophenol
Ausbeute 62.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CCNc2cc([N+](=O)[O-])ccc21
Reaction #161225
4,4-dimethyl-7-nitro-1,2,3,4-tetrahydro-quinoline
Ausbeute 50.9%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(C)(C)c2ccc(N)cc21
Reaction #161226
tert-butyl 7-amino-3,4-dihydro-4,4-dimethylquinoline-1(2H)-carboxylate
Ausbeute 95.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CCCNc2cc([N+](=O)[O-])ccc21
Reaction #161230
5,5-dimethyl-8-nitro-2,3,4,5-tetrahydro-1H-benzo[b]azepine
Ausbeute 86.8%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N1CCCC(C)(C)c2ccc([N+](=O)[O-])cc21
Reaction #161231
1-(5,5-dimethyl-8-nitro-2,3,4,5-tetrahydrobenzo[b]azepin-1-yl)ethanone
Ausbeute 73.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N1CCCC(C)(C)c2ccc(N)cc21
Reaction #161232
1-(8-amino-2,3,4,5-tetrahydro-5,5-dimethylbenzo[b]azepin-1-yl)ethanone
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #161233
2′,3′-dihydro-carboxylic acid tert-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N1CC(C)(C)c2ccc([N+](=O)[O-])cc21
Reaction #161238
1-(3,3-dimethyl-6-nitroindolin-1-yl)ethanone
Ausbeute 88.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N1CC(C)(C)c2ccc(N)cc21
Reaction #161239
1-(6-amino-3,3-dimethyl-2,3-dihydro-indol-1-yl)-ethanone
Ausbeute 70.7%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1ccc([N+](=O)[O-])cc1S(=O)(=O)Cl
Reaction #161257
2-tert-butyl-5-nitrobenzene-1-sulfonyl chloride
Ausbeute 17.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Nc1ccc2c(c1)NC(=O)CC2(C)C
Reaction #175239
DOI: 10.1039/C8SC04228D
CC1(C)CCCNc2cc(N)ccc21
Reaction #178084
DOI: 10.1039/C8SC04228D
CCOC(=O)CCCCN1C(=O)C(C)(C)c2cc(NC(=O)CCc3ccccc3)c([N+](=O)[O-])cc21
Reaction #181302
DOI: 10.1039/C8SC04228D
CC(C)(C)c1ccc([N+](=O)[O-])cc1N
Reaction #183845
DOI: 10.1039/C8SC04228D
CC1(C)CNc2cc([N+](=O)[O-])ccc21
Reaction #184617
DOI: 10.1039/C8SC04228D
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