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COC(=O)c1ccncc1

CCc1cccc(CNC[C@@H](O)[C@H](Cc2cc(F)cc(F)c2)NC(=O)c2ccc3c(c2)C(O)CC3)c1
Reaction #42410
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccncc1O
Reaction #44981
ethyl 3-hydroxyisonicotinate
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cncc(O)c1C(=O)OC
Reaction #65741
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cc(C)[nH]c(=O)c1C(=O)OCC
Reaction #65752
3,4-Diethoxycarbonyl-6-methyl-2-pyridone
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1c(F)nc(-c2ccccc2)c(N)c1C(=O)OCC
Reaction #65771
3-Amino-6-fluoro-4,5-diethoxycarbonyl-2-phenylpyridine
DOI: 10.6084/m9.figshare.5104873.v1
Nc1c(-c2ccccc2)nc(F)c2c(=O)[nH][nH]c(=O)c12
Reaction #65772
8-Amino-5-fluoro-7-phenylpyrido[3,4-d]pyridazine-1,4(2H,3H)dione
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(Br)ncc1F
Reaction #67789
methyl 2-bromo-5-fluoroisonicotinate
Выход 81.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(C)ncc1F
Reaction #67790
Methyl 5-fluoro-2-methylisonicotinate
DOI: 10.6084/m9.figshare.5104873.v1
CCc1[nH]c(C(=O)N[C@H]2CCN(c3cc(C(=O)OC)cc(Cl)n3)C[C@H]2OC)nc1Cl
Reaction #72069
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C1OC(=O)c2cnccc21
Reaction #80681
3,4-pyridine dicarboxylic acid anhydride
Выход 76.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1ccncc1C(=O)c1cc(F)ccc1F
Reaction #80682
3-(2',5'-difluorobenzoyl)isonicotinic acid
Выход 84.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(OC1CCC(Oc2ccc3c(c2)CCC(c2ccccc2)O3)CC1)c1ccncc1F
Reaction #88058
title compound
Выход 68.4%DOI: 10.6084/m9.figshare.5104873.v1
C[n+]1c2ccccc2c(C(=O)Oc2ccc(O[Si](C)(C)C(C)(C)C)cc2)c2ccccc21.O=S(=O)([O-])C(F)(F)F
Reaction #155392
4-(tert-butyldimethylsilyloxy)phenyl 10-methylacridinium-9-carboxylate trifluoromethanesulfonate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc(-n2ccc(C(=O)O)cc2=O)cc1
Reaction #158904
1-(4-Ethoxycarbonyl-phenyl)-2-oxo-1,2-dihydro-pyridine-4-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(Cl)ncc1[N+](=O)[O-]
Reaction #164573
methyl 2-chloro-5-nitroisonicotinate
Выход 90.2%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(N2CCN3CCC2CC3)ncc1[N+](=O)[O-]
Reaction #164574
methyl 2-(1,4-diazabicyclo[3.2.2]nonan-4-yl)-5-nitroisonicotinate
DOI: 10.6084/m9.figshare.5104873.v1
CNC(=O)c1cc(N2CCN3CCC2CC3)ncc1[N+](=O)[O-]
Reaction #164575
2-(1,4-diazabicyclo[3.2.2]nonan-4-yl)-N-methyl-5-nitroisonicotinamide
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1cc(N2CCN3CCC2CC3)ncc1[N+](=O)[O-]
Reaction #164576
2-(1,4-diazabicyclo[3.2.2]nonan-4-yl)-5-nitroisonicotinic acid
Выход 55.6%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(Br)ncc1F
Reaction #165954
methyl 2-bromo-5-fluoroisonicotinate
Выход 81.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(C)ncc1F
Reaction #165955
Methyl 5-fluoro-2-methylisonicotinate
DOI: 10.6084/m9.figshare.5104873.v1
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