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14112

Brc1cccc2c1-c1ccccc1C2
Reaction #11037
4-bromo-fluorene
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #42259
solid
Ausbeute 31.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #45531
solid
Ausbeute 31.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CCOc1c(C(C)(C)C)cc(C)cc1[Si](C)(C)C1c2cc(C(C)(C)C)ccc2-c2ccc(C(C)(C)C)cc21
Reaction #266547
DOI: 10.1039/C8SC04228D
CC1=CC(C(C)(C)C)=CC1C(C)(C)c1c(C(C)(C)C)ccc2c1Cc1cc(C(C)(C)C)ccc1-2
Reaction #358194
powdery white solid
Ausbeute 71.5%DOI: 10.6084/m9.figshare.5104873.v1
CC1=Cc2ccccc2C1C=CC1c2cc(C(C)(C)C)ccc2-c2ccc(C(C)(C)C)cc21
Reaction #466519
aimed product
Ausbeute 93.1%DOI: 10.6084/m9.figshare.5104873.v1
CCCCC1=CCC(C(c2ccccc2)(c2ccccc2)C2c3cc(C(C)(C)C)ccc3-c3ccc(C(C)(C)C)cc32)=C1
Reaction #563471
desired product
Ausbeute 171.2%DOI: 10.6084/m9.figshare.5104873.v1
CCCCC1=CCC(C(C)(C)C2c3cc(C(C)(C)C)ccc3-c3ccc(C(C)(C)C)cc32)=C1
Reaction #563472
desired product
Ausbeute 153.4%DOI: 10.6084/m9.figshare.5104873.v1
CC1=CC(C(C)(C)C)=CC1C(C)(C)c1c(C(C)(C)C)ccc2c1Cc1cc(C(C)(C)C)ccc1-2
Reaction #582934
powdery white solid
Ausbeute 71.5%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #587132
solid
Ausbeute 31.0%DOI: 10.6084/m9.figshare.5104873.v1
[Li][c]1c(C(C)(C)C)ccc2c1Cc1cc(C(C)(C)C)ccc1-2
Reaction #692141
2,7-di-tert-butylfluorenyl lithium
DOI: 10.6084/m9.figshare.5104873.v1
CC1=Cc2ccccc2C1C=CC1c2cc(C(C)(C)C)ccc2-c2ccc(C(C)(C)C)cc21
Reaction #699610
aimed product
Ausbeute 93.1%DOI: 10.6084/m9.figshare.5104873.v1
C=CCOc1c(C(C)(C)C)cc(C)cc1[Si](C)(C)C1c2cc(C(C)(C)C)ccc2-c2ccc(C(C)(C)C)cc21
Reaction #748945
(2-allyloxy-3-tert-butyl-5-methylphenyl)(2,7-di-tert-butylfluoren-9-yl)dimethylsilane
DOI: 10.6084/m9.figshare.5104873.v1
C=CCOc1c(C(C)(C)C)cc(C)cc1[Si](CC)(CC)C1c2cc(C(C)(C)C)ccc2-c2ccc(C(C)(C)C)cc21
Reaction #748946
(2-allyloxy-3-tert-butyl-5-methylphenyl)(2,7-di-tert-butyl fluoren-9-yl)diethylsilane
DOI: 10.6084/m9.figshare.5104873.v1
C=CCOc1c([SiH](C)CCC2c3cc(C(C)(C)C)ccc3-c3ccc(C(C)(C)C)cc32)cc(C)cc1C(C)(C)C
Reaction #748947
(2-allyloxy-3-tert-butyl-5-methylphenyl)(2,7-di-tert-butyl fluoren-9-yl)ethylmethylsilane
DOI: 10.6084/m9.figshare.5104873.v1
C=CCOc1c([SiH](CC2c3cc(C(C)(C)C)ccc3-c3ccc(C(C)(C)C)cc32)c2ccccc2)cc(C)cc1C(C)(C)C
Reaction #748948
(2-allyloxy-3-tert-butyl-5-methylphenyl)(2,7-di-tert-butyl fluoren-9-yl)methylphenylsilane
DOI: 10.6084/m9.figshare.5104873.v1
C=CCOc1c(C(C)(C)C)cc(C)cc1[Si](CCC)(CCC)C1c2cc(C(C)(C)C)ccc2-c2ccc(C(C)(C)C)cc21
Reaction #748949
(2-allyloxy-3-tert-butyl-5-methylphenyl)(2,7-di-tert-butylfluoren-9-yl)di-n-propylsilane
Ausbeute 20.8%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1ccc2c(c1)Cc1c-2ccc(C(C)(C)C)c1[Si](Cl)(C1CCCCC1)C1CCCCC1
Reaction #834156
chlorodicyclohexyl(2,7-di-tert-butylfluorenyl)silane
Ausbeute 101.8%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(C(c2ccc(C)cc2)(c2c(C(C)(C)C)ccc3c2Cc2cc(C(C)(C)C)ccc2-3)C2C=CC=C2)cc1
Reaction #834160
(2,7-di-tert-butylfluorenyl)cyclopentadienyl di-p-tolyl methane
Ausbeute 67.5%DOI: 10.6084/m9.figshare.5104873.v1
c1ccc2c(c1)Cc1ccccc1-2
Reaction #1172953
fluorene
DOI: 10.6084/m9.figshare.5104873.v1
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