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Cc1cccc(C(=O)O)c1N

O=C(O)c1cc([N+](=O)[O-])cc2c1NCC2
Reaction #5026
compound
Выход 77.1%DOI: 10.6084/m9.figshare.5104873.v1
O=C(OCc1ccccc1)c1cc(Br)cc2c1NCCCC2
Reaction #5028
compound
Выход 99.7%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1cc2c(c(C(=O)O)c1)NCCCC2
Reaction #5029
compound
Выход 85.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc([N+](=O)[O-])cc2c1NCCCC2
Reaction #5030
compound
Выход 100.4%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1cccc2c1NCC2
Reaction #6461
indoline-7-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1cccc(-c2ccn3ccccc23)c1[N+](=O)[O-].c1ccc(-c2ccccc2)cc1
Reaction #50333
biphenyl indolizinyl nitrobenzoate
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cccc(C)c1N
Reaction #62030
methyl 2-amino-3-methylbenzoate
Выход 92.3%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cccc2cn[nH]c12.Cl
Reaction #62031
methyl 1H-indazole-7-carboxylate hydrochloride
Выход 68.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1cc(C(=O)Cl)c([N+](=O)[O-])c(C(C)(C)C)c1
Reaction #81073
3,5-Di-t-butyl-2-nitrobenzoyl chloride
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(F)cc(C(=O)O)c1N
Reaction #89545
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(F)c(C(=O)O)c1N
Reaction #89551
desired product
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(Cl)cc(C(=O)O)c1N
Reaction #90212
desired intermediate
Выход 75.5%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(Cl)cc2c(=O)oc(-c3cc(Cl)nn3-c3ncccc3Cl)nc12
Reaction #90218
title product
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(Cl)cc2c(=O)oc(-c3cc(Br)nn3-c3ncccc3Cl)nc12
Reaction #90223
title product
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(Cl)cc2c(=O)oc(=O)[nH]c12
Reaction #90234
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(Cl)cc2c(=O)oc(-c3cc(Br)nn3-c3ncccc3Cl)nc12
Reaction #90237
title product
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(Cl)cc2c(=O)oc(-c3cc(Cl)nn3-c3ncccc3Cl)nc12
Reaction #90238
title product
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCc1ccc(OC(=O)c2ccc3c(c2N)C(=O)c2ccc(C)c(N)c2C3=O)cc1
Reaction #93455
1,5-diamino-6-methyl-2-anthraquinonecarboxylic acid p-heptylphenyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cc(C)c([N+](=O)[O-])cc1[N+](=O)[O-]
Reaction #161137
5-methyl-2,4-dinitro-benzoic acid ethyl ester
Выход 25.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N1CCN(c2cccc(C3Nc4c(cc(Cl)cc4C(=O)O)CC3(C)C)c2)CC1
Reaction #176142
DOI: 10.1039/C8SC04228D
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