子结构搜索

Nc1ccccc1C=O

O=C(O)c1cc([N+](=O)[O-])cc2c1NCC2
Reaction #5026
compound
收率 77.1%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccccc1C(=O)Nc1ccccn1
Reaction #40405
(2-aminophenyl)-N-(2-pyridyl)carboxamide
DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccccc1C(=O)Nc1ccccn1
Reaction #40432
(2-aminophenyl)-N-(2-pyridyl)carboxamide
DOI: 10.6084/m9.figshare.5104873.v1
Nc1c(C(=O)C2CCCCC2)cc(-c2cccnc2)cc1[N+](=O)[O-]
Reaction #40530
title compound
收率 89.0%DOI: 10.6084/m9.figshare.5104873.v1
CCC(=O)N1CC(=CN(C)C)C(=O)c2cc([N+](=O)[O-])ccc21
Reaction #63949
3-dimethylaminomethylene-6-nitro-4-oxo-1-propionyl-1,2,3,4-tetrahydroquinoline
收率 92.0%DOI: 10.6084/m9.figshare.5104873.v1
CCC(=O)N1CCC(=O)c2cc(N)ccc21
Reaction #63954
6amino-4-oxo-1-propionyl-1,2,3,4-tetrahydroquinoline
收率 90.1%DOI: 10.6084/m9.figshare.5104873.v1
CCC(=O)N1Cc2cn[nH]c2-c2cc([N+](=O)[O-])ccc21
Reaction #63959
4,5-dihydro-8-nitro-5-propionyl-1H-pyrazolo[4,3-c]quinoline
收率 93.0%DOI: 10.6084/m9.figshare.5104873.v1
O=Cc1ccc(-c2ccc(C(=O)N3CCCC3)cc2)cc1[N+](=O)[O-]
Reaction #66261
3-nitro-4′-(pyrrolidine-1-carbonyl)biphenyl-4-carbaldehyde
收率 178.9%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1ccc(C(=O)O)c([N+](=O)[O-])c1
Reaction #155634
4-tert-Butyl-2-nitro-benzoic acid
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1ccc(C(=O)O)c(N)c1
Reaction #155635
2-Amino-4-tert-butyl-benzoic acid
收率 10.3%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
收率 25.4%DOI: 10.6084/m9.figshare.5104873.v1
CONC(=O)c1ccc2[nH]ncc2c1Nc1ccc(I)cc1F
Reaction #166251
title compound
收率 44.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cccc2c1C(=O)CCCN2C(=O)OC(C)C
Reaction #173456
DOI: 10.1039/C8SC04228D
CC1CC(=O)C(C(=O)c2ccc(C(F)(F)F)cc2[N+](=O)[O-])C(=O)O1
Reaction #174844
DOI: 10.1039/C8SC04228D
CCc1ccc(Nc2c(C(=O)NOCCO)ccc(F)c2F)c(F)c1
Reaction #175802
DOI: 10.1039/C8SC04228D
NC(=O)c1cc(C(=O)c2ccccc2)ccc1N
Reaction #177147
DOI: 10.1039/C8SC04228D
O=C(NCCO)c1c([N+](=O)[O-])cc([N+](=O)[O-])cc1[N+](=O)[O-]
Reaction #194903
DOI: 10.1039/C8SC04228D
CCN(CC)C(=CC(=O)c1ccc(C(F)(F)F)cc1[N+](=O)[O-])C1CC1
Reaction #197621
DOI: 10.1039/C8SC04228D
NC(=NO)c1ncn2c1C1CCN1C(=O)c1c(Br)cccc1-2
Reaction #200146
DOI: 10.1039/C8SC04228D
COc1ccc(CN2Cc3c(C(=N)NO)ncn3-c3ccc(Cl)cc3C2=O)c(OC)c1
Reaction #202003
DOI: 10.1039/C8SC04228D
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