Busqueda de Subestructura

CC(C)n1cc(-c2ccc(F)cc2)c2ccccc21

CC(C)n1c(C=CC=O)c(-c2ccc(F)cc2)c2ccccc21
Reaction #10032
3-[3-(4-Fluorophenyl)-1-(1-Methylethyl)-1H-Indol-2-yl]-2-Propenal
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)n1c(C=CC=O)c(-c2ccc(F)cc2)c2ccccc21
Reaction #10034
3-[3-(4-Fluorophenyl)-1-(1-Methylethyl)-1H-Indol-2-yl]-2-Propenal
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)n1c(C=CC=O)c(-c2ccc(F)cc2)c2ccccc21
Reaction #10035
product
Rendimiento 69.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)n1c(/C=C/C(O)CC(O)CC(=O)[O-])c(-c2ccc(F)cc2)c2ccccc21.[Na+]
Reaction #75872
Fluvastatin sodium
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)NCCN1CCC(n2cc(-c3ccc(F)cc3)c3cc(C)ccc32)CC1
Reaction #194819
DOI: 10.1039/C8SC04228D
CC(C)n1c(C=O)c(-c2ccc(F)cc2)c2ccccc21
Reaction #226759
DOI: 10.1039/C8SC04228D
Cc1ccc2c(c1)c(-c1ccc(F)cc1)c(Cl)n2C1CCN(CCN2CCN(C(C)C)C2=O)CC1
Reaction #262395
DOI: 10.1039/C8SC04228D
COC(=O)C(=O)c1ccc(OCC=Cc2c(-c3ccc(F)cc3)c3ccccc3n2C(C)C)cc1
Reaction #264498
DOI: 10.1039/C8SC04228D
CNCCN1CCC(n2cc(-c3ccc(F)cc3)c3cc(C)ccc32)CC1
Reaction #279343
DOI: 10.1039/C8SC04228D
CON(C)C(=O)CC1CC(C=Cc2c(-c3ccc(F)cc3)c3ccccc3n2C(C)C)OC(C)(C)O1
Reaction #280627
DOI: 10.1039/C8SC04228D
COc1ccc(CN2CCN(C(c3ccc(F)cc3)c3ccc(F)cc3)CC2)c(OC)c1OC
Reaction #307191
iomerizine
DOI: 10.6084/m9.figshare.5104873.v1
Fc1ccc(-c2cn(C3CCNCC3)c3cc(Cl)ccc23)cc1
Reaction #362536
title compound
Rendimiento 81.8%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2c(c1)c(-c1ccc(F)cc1)c(C)n2C1CCN(CCN2CCNC2=O)CC1
Reaction #362538
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2c(c1)c(-c1ccc(F)cc1)c(C)n2C1CCN(CCN2CCNC2=O)CC1
Reaction #362539
indole
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2c(c1)c(-c1ccc(F)cc1)c(C)n2C1CCN(C)CC1
Reaction #362540
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)N1CCC(n2cc(-c3ccc(F)cc3)c3cc(C)ccc32)CC1
Reaction #362541
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)NCCN1CCC(n2cc(-c3ccc(F)cc3)c3cc(C)ccc32)CC1
Reaction #362542
1-[1-(N-methoxycarbonyl-2-aminoethyl)-4piperidyl]-3-(4-fluorophenyl)-5-methyl-1H-indole
DOI: 10.6084/m9.figshare.5104873.v1
CNCCN1CCC(n2cc(-c3ccc(F)cc3)c3cc(C)ccc32)CC1
Reaction #362543
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CN1CCC(n2cc(-c3ccc(F)cc3)c3cc(C)ccc32)CC1
Reaction #362544
methyl 4-[3-(4-fluorophenyl)-5-methyl-1H-indol-1-yl]1-piperidinacetate
DOI: 10.6084/m9.figshare.5104873.v1
O=C(OCC(Cl)(Cl)Cl)N1CCC(n2cc(-c3ccc(F)cc3)c3ccccc32)CC1Br
Reaction #362551
2,2,2-trichloroethyl 2-bromo-4-[3-(4-fluorophenyl)-1H-indol-1-yl]piperidine-1-carboxylate
Rendimiento 95.2%DOI: 10.6084/m9.figshare.5104873.v1
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