Busqueda de Subestructura

Clc1cc(-c2ccccc2)c2ccccc2n1

O=C1c2cc3c(cc2-c2c1c(Cl)nc1ccccc21)OCO3
Reaction #3245
title compound
Rendimiento 59.9%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2c3c(c(Cl)nc2c1)C(=O)c1ccccc1-3
Reaction #3248
title compound
Rendimiento 73.4%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)CCNc1nc2cc(F)ccc2c2c1C(=O)c1ccccc1-2.Cl.Cl
Reaction #3251
title compound
Rendimiento 68.6%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)CCOc1nc2ccccc2c2c1C(=O)c1cc3c(cc1-2)OCO3
Reaction #3255
title compound
Rendimiento 68.1%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc(Sc2cc(-c3ccccc3)c3ccccc3n2)cc1
Reaction #83344
2-(4-aminophenylthio)-4-phenylquinoline
Rendimiento 451.6%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(C)(C)CCCCSc1cc(-c2ccccc2)c2ccccc2n1
Reaction #176685
DOI: 10.1039/C8SC04228D
O=C(NCC(F)(F)F)C1(CCCCN2CCN(c3cc(-c4ccccc4)c4ccccc4n3)CC2)c2ccccc2-c2ccccc21
Reaction #178115
DOI: 10.1039/C8SC04228D
[N-]=[N+]=NCc1ccc2c(-c3ccc(F)cc3)cc(Cl)nc2c1
Reaction #194418
DOI: 10.1039/C8SC04228D
Fc1ccc(-c2cc(Cl)nc3cc(CBr)ccc23)cc1
Reaction #200192
DOI: 10.1039/C8SC04228D
CCC(O)(c1cn(Cc2ccc3c(-c4ccc(F)cc4)cc(-c4ccccc4)nc3c2)nn1)C(F)(F)F
Reaction #200973
DOI: 10.1039/C8SC04228D
NNc1cc(-c2ccccc2)c2ccccc2n1
Reaction #202770
DOI: 10.1039/C8SC04228D
Cc1ccc2c3c(c(Cl)nc2c1)C(=O)c1ccccc1-3
Reaction #241593
DOI: 10.1039/C8SC04228D
C=C(OCC)c1cc(-c2cccc(Cl)c2)c2cc(C(O)(c3ccc(Cl)cc3)c3cncn3C)ccc2n1
Reaction #291942
DOI: 10.1039/C8SC04228D
CCC(O)(c1cn(Cc2ccc3c(-c4ccc(F)cc4)cc(SC)nc3c2)nn1)C(F)(F)F
Reaction #384554
DOI: 10.1039/C8SC04228D
Cc1ccc2c3c(c(Cl)nc2c1)C(=O)c1ccccc1-3
Reaction #387955
DOI: 10.1039/C8SC04228D
Clc1cccc(-c2cc(Cl)nc3ccc(Br)cc23)c1
Reaction #405605
DOI: 10.1039/C8SC04228D
Cl.O=C(c1ccc(Cl)cc1)c1ccc2nc(Cl)cc(-c3cccc(Cl)c3)c2c1
Reaction #434159
[2-chloro-4(3-chlorophenyl)-6-quinolinyl](4-chlorophenyl)-methanone hydrochloride
Rendimiento 100.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-c2cccc(Cl)c2)c2cc(C(=O)c3ccc(Cl)cc3)ccc2n1
Reaction #434160
(4-chlorophenyl)[4-(3-chlorophenyl)-2-methoxy-6-quinolinyl]-methanone
Rendimiento 62.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1nc2ccccc2c(-c2ccccc2)c1C(=O)N(C)Cc1cc(C(F)(F)F)cc(C(F)(F)F)c1
Reaction #462175
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CNc1nc2ccccc2c(-c2ccccc2)c1C(=O)N(C)Cc1cc(C(F)(F)F)cc(C(F)(F)F)c1
Reaction #462176
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Página 1Siguiente