Busqueda de Subestructura

15723

CC(=O)c1cc2ccccc2cn1
Reaction #1027
3-acetyl-isoquinoline
Rendimiento 14.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=NO)c1cc2ccccc2cn1
Reaction #1028
3-acetyl-isoquinoline oxime
Rendimiento 89.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)CC(O)(c1ccccc1)c1ccccn1
Reaction #7314
tert-butyl 3-hydroxy-3-phenyl-3-(pyridin-2-yl)propionate
Rendimiento 98.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1cccc(-c2cccc(C(=O)c3ccccn3)c2)c1OCc1ccccc1
Reaction #73725
(2′-(Benzyloxy)-3′-tert-butylbiphenyl-3-yl)(pyridin-2-yl)methanone
DOI: 10.6084/m9.figshare.5104873.v1
C=C(c1cccc(-c2cccc(C(C)(C)C)c2OCc2ccccc2)c1)c1ccccn1
Reaction #73726
12
Rendimiento 16.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cccnc1C(=O)c1ccc(F)c(N)c1
Reaction #77252
title compound
Rendimiento 73.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)c1ccc2ccccc2n1
Reaction #80821
2-acetylquinoline
Rendimiento 96.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(O)C1CCc2ccccc2N1
Reaction #80822
2-(1-hydroxyethyl)tetrahydroquinoline
Rendimiento 78.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)c1ccc2ccccc2n1
Reaction #80823
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)c1cccc(CC#CO)n1
Reaction #81487
2-acetyl-6-(3-hydroxy-2-propynyl)pyridine
Rendimiento 50.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)c1cccc(CCCO)n1
Reaction #81488
2-acetyl-6-(3-hydroxypropyl)-pyridine
Rendimiento 84.6%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cn1ccnc1)c1ccc(Cl)cn1
Reaction #82790
2-[2'-(1H-Imidazol-1-yl)acetyl]-5-chloropyridine
DOI: 10.6084/m9.figshare.5104873.v1
OC(Cn1ccnc1)c1ccc(Cl)cn1
Reaction #82791
1-(5-Chloro-2-pyridyl)-2-(1H-imidazol-1-yl)ethane-1-ol
DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C=CC(=O)c1ccc(Cl)c(C#N)n1
Reaction #84174
compound 67
Rendimiento 35.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cccnc1C(C)=O
Reaction #88891
title compound
Rendimiento 63.6%DOI: 10.6084/m9.figshare.5104873.v1
COc1nc(C(=O)c2ccc(OC(C)C)c(Cl)c2)ccc1Cl
Reaction #157681
title compound
Rendimiento 93.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2c(Oc3cc4ccccc4nc3C(C)=O)ccnc2cc1OCCCO
Reaction #183040
DOI: 10.1039/C8SC04228D
O=C(CC(=O)C1CC1)c1ccccn1
Reaction #183176
DOI: 10.1039/C8SC04228D
Cc1ccnc(C(=O)c2cn(-c3cccc(-c4cccnc4F)c3)cn2)c1
Reaction #191985
DOI: 10.1039/C8SC04228D
O=C(c1ccccn1)c1cnc2c(C(F)(F)F)cccc2c1-c1ccc(Cl)cc1
Reaction #196756
DOI: 10.1039/C8SC04228D
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