Busqueda de Subestructura

32549

CCCCCC[C@@H](F)COc1c(F)cc(-c2ccc([C@H]3CC[Si@H](CCC)CC3)cc2)cc1F
Reaction #2740
(R)-4-(4-(trans-4-n-propyl-4-silacyclohexyl)phenyl)-1-(2-fluorooctyloxy)2,6-difluorobenzene
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCC[Si@H]1CC[C@H](c2ccc(-c3cc(F)c(OC[C@@H](F)CCCCCC)c(F)c3)cc2)CC1
Reaction #2742
(S)-4-(4-(trans-4-n-nonyl-4-silacyclohexyl)phenyl)-1-(2-fluorooctyloxy)-2,6-difluorobenzene
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cc(F)cc(-c2cc(Br)c3c(c2)C2(CCCCC2)C(=O)N3)c1
Reaction #7100
title compound
Rendimiento 43.0%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(-c2ccc3c(c2)C2(CCCCC2)C(=O)N3)cc1F
Reaction #7103
title compound
Rendimiento 37.0%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cc(-c2ccc3c(c2)C2(CCCC2)C(=O)N3)ccc1F
Reaction #7110
title compound
Rendimiento 10.5%DOI: 10.6084/m9.figshare.5104873.v1
O=C1Nc2ccc(-c3ccc(F)c(Cl)c3)cc2C12CCCC2
Reaction #7111
title compound
Rendimiento 66.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(c1ccccn1)c1cccc(-c2ccccc2)c1O
Reaction #73697
3-(1-(Pyridin-2yl)ethyl)biphenyl-2-ol
DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1ccc(-c2ccccc2Cc2cccc(F)c2)cc1
Reaction #77459
title compound
Rendimiento 83.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1CC[C@H]2[C@@H](C1)c1cc(-c3c(F)cccc3F)cc3c1N2CCC3
Reaction #79306
title compound
Rendimiento 62.7%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CNCCCNCCCNCc1cc(CNCCCNCCCNCC(C)C)cc(-c2ccccc2)c1
Reaction #87264
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CNCCCNCCCNCc1cc(CNCCCNCCCNCC(C)C)cc(-c2ccccc2)c1.Cl
Reaction #87265
desired product
Rendimiento 50.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CNCCCNCCCNCc1cc(CNCCCNCCCNCC(C)C)cc(-c2ccccc2)c1
Reaction #87267
N1,N1′-([1,1′-Biphenyl]-3,5-diylbis(methylene))bis(N3-(3-(isobutylamino)propyl)propane-1,3-diamine)
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CNCCCNCCCNCc1cc(CNCCCNCCCNCC(C)C)cc(-c2ccccc2)c1.Cl
Reaction #87268
desired product
Rendimiento 89.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CNCCCNCCCNCc1cccc(-c2cc(CNCCCNCCCNCC(C)C)cc(CNCCCNCCCNCC(C)C)c2)c1.Cl
Reaction #87276
desired product
Rendimiento 52.0%DOI: 10.6084/m9.figshare.5104873.v1
[Br-].c1ccc(-c2ccc(CCCCC[n+]3cccc4ccccc43)cc2)cc1
Reaction #171536
title compound
Rendimiento 64.0%DOI: 10.6084/m9.figshare.5104873.v1
[Br-].c1ccc(-c2ccc(CCCCC[n+]3ccc4ccccc4c3)cc2)cc1
Reaction #171537
title compound
Rendimiento 61.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CC(C(=O)O)c1cc(C#N)c(OCC2CC2)c(-c2ccc(C(F)(F)F)cc2)c1
Reaction #173492
DOI: 10.1039/C8SC04228D
CCCCCCCCc1ccc(-c2ccc(COc3ccc(OCC(C)OC(=O)OCCCC)cc3)cc2)cc1
Reaction #175740
DOI: 10.1039/C8SC04228D
C=CC(=O)OCCCCCCOc1ccc(-c2ccc(C3CCC(CCCO)CC3)cc2)cc1
Reaction #183535
DOI: 10.1039/C8SC04228D
O=c1c(Nc2ccccc2O)c(Nc2ccccc2-c2ccccc2)c1=O
Reaction #186854
DOI: 10.1039/C8SC04228D
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