Busqueda de Subestructura

c1ccc2c(c1)CCCN2

CC1(C)CCNc2ccc(Br)cc21
Reaction #6651
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CCNc2ccc(C#C[Si](C)(C)C)cc21
Reaction #6652
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CC(=O)Nc2ccccc21
Reaction #40658
1a
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CCNc2ccccc21
Reaction #40659
1b
Rendimiento 93.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CCN(C=O)c2ccc(Br)cc21
Reaction #52405
title compound
Rendimiento 90.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CCN(C2CC2)c2ccc(Br)cc21
Reaction #52406
title compound
Rendimiento 64.0%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
Rendimiento 92.0%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
Rendimiento 93.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CC(=O)Nc2cc(-c3nc4ccccc4[nH]3)ccc21
Reaction #64676
title compound
Rendimiento 37.2%DOI: 10.6084/m9.figshare.5104873.v1
CCN1C(=O)CC(C)(C)c2ccc(C#N)cc21
Reaction #64677
4,4-dimethyl-1-ethyl-1,2,3,4-tetrahydro-2-oxo-7-quinolinecarbonitrile
Rendimiento 48.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)N[C@@H]1Cc2ccccc2N(OC)C1=O
Reaction #75425
title compound
Rendimiento 99.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C1CC(c2ccccc2)c2c(Cl)cc(Cl)cc2N1
Reaction #75648
Compound 15
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cccc(C2CC(C(=O)O)Nc3cc(Cl)cc(Cl)c32)c1
Reaction #75650
Compound 18
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(C2CC(C(=O)O)Nc3cc(Cl)cc(Cl)c32)cc1
Reaction #75652
Compound 20
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C1CC(c2ccc(F)cc2)c2c(Cl)cc(Cl)cc2N1
Reaction #75663
Compound 31
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C1CC(c2cccc(Br)c2)c2c(Cl)cc(Cl)cc2N1
Reaction #75670
Compound 38
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CC(c2ccc(Br)cc2)c2c(Cl)cc(Cl)cc2N1
Reaction #75671
Compound 39
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C1CC(c2ccc(Br)cc2)c2c(Cl)cc(Cl)cc2N1
Reaction #75672
Compound 40
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CC(c2ccccc2Cl)c2cc(Cl)ccc2N1
Reaction #75684
Compound 52
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(=O)N(C)c1c([N+](=O)[O-])ccc2c1CCCN2
Reaction #76517
[Methyl(1,2,3,4-tetrahydro-6-nitro-5-quinolinyl)-amino]oxo-acetic acid ethyl ester
Rendimiento 93.0%DOI: 10.6084/m9.figshare.5104873.v1
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