Recherche de Sous-structure

CCC1=Cc2ccccc2C1

CCC1=Cc2c(cccc2-c2ccccc2)C1
Reaction #1354
desired product
Rendement 73.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CC1=Cc2c(cccc2-c2cccc3ccccc23)C1
Reaction #1361
desired product
Rendement 93.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1C=CC=C2C1=Cc1ccccc12
Reaction #7429
Fluorenone
DOI: 10.6084/m9.figshare.5104873.v1
c1ccc(-c2ccccc2-c2ccc3c(c2)C2(c4cc(-c5ccccc5-c5ccccc5)ccc4-c4c(-c5ccccc5-c5ccccc5)cc(-c5ccccc5-c5ccccc5)cc42)c2cc(-c4ccccc4-c4ccccc4)cc(-c4ccccc4-c4ccccc4)c2-3)cc1
Reaction #8644
2,2′,4,4′,7,7′-hexabiphenylyl-9,9′-spirobifluorene
DOI: 10.6084/m9.figshare.5104873.v1
O=C1C=CC=C2C1=Cc1ccccc12
Reaction #9838
fluorenon
DOI: 10.6084/m9.figshare.5104873.v1
O=C1C=CC=C2C1=Cc1ccccc12
Reaction #9840
fluorenon
DOI: 10.6084/m9.figshare.5104873.v1
C1=C(Cc2ccccc2)Cc2ccccc21
Reaction #12060
2-benzylindene
DOI: 10.6084/m9.figshare.5104873.v1
C1=C(CC2CCCCC2)Cc2ccccc21
Reaction #12061
2-(cyclohexylmethyl)indene
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)N[Si](C)(C)C1C(CC2CCCCC2)=Cc2ccccc21
Reaction #12062
yellow oil
Rendement 90.0%DOI: 10.6084/m9.figshare.5104873.v1
Fc1ccc(CC2=Cc3ccccc3C2)cc1
Reaction #12063
2-(4-fluorophenylmethyl)indene
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)N[Si](C)(C)C1C(Cc2ccc(F)cc2)=Cc2ccccc21
Reaction #12064
yellow oil
Rendement 97.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)N[Si](C)(C)C1C(CC(C)(C)c2ccccc2)=Cc2ccccc21
Reaction #12066
yellow oil
Rendement 96.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)CC1=Cc2ccccc2C1
Reaction #12067
2-neopentylindene
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)CC1=Cc2ccccc2C1[Si](C)(C)NC(C)(C)C
Reaction #12068
yellow oil
Rendement 103.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C1C(Br)=CC=C2C1=Cc1ccccc12
Reaction #53765
yellow solid
Rendement 92.9%DOI: 10.6084/m9.figshare.5104873.v1
CCCCC1=C(OC)c2cc3c(cc2C1)OCO3
Reaction #62986
2-n-butyl-3-methoxy-5,6-methylenedioxyindene
Rendement 90.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCC1=C(Br)c2cc3c(cc2C1)OCO3
Reaction #62987
2-n-butyl-3-bromo-5,6-methylenedioxyindene
Rendement 68.2%DOI: 10.6084/m9.figshare.5104873.v1
CCCCC1=C(N(CC)CC)c2cc3c(cc2C1)OCO3
Reaction #62991
2-n-butyl-3-diethylamino-5,6-methylenedioxyindene
Rendement 65.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)C2=C(C=CC(N(c3ccccc3)c3ccccc3)C2=O)c2ccccc21
Reaction #64834
2-(N,N-diphenyl)amino-9,9-dimethylfluorenone
Rendement 79.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #75085
fluorenone ketyl
DOI: 10.6084/m9.figshare.5104873.v1
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