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17110

CC(C)(C)c1cc2c(cc1-c1ccccc1)Cc1cc(-c3ccccc3)c(C(C)(C)C)cc1-2
Reaction #11038
2,7-diphenyl-3,6-di-t-butyl-fluorene
収率 179.4%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc2c(cc1C(C)(C)C)-c1cc(C(C)(C)C)ccc1C2
Reaction #11039
solid
収率 102.9%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc2c(cc1C(C)(C)C)-c1cc(C(C)(C)C)c(C)cc1C2
Reaction #11040
2,7-di-methyl-3,6-di-tert-butyl-fluorene
収率 85.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc2c(cc1C(C)(C)C)-c1cc(C(C)(C)C)ccc1C2
Reaction #288287
DOI: 10.1039/C8SC04228D
CC1(C)CCC(C)(C)c2cc3c(cc21)Cc1cc2c(cc1-3)C(C)(C)CCC2(C)C
Reaction #358172
powder
収率 53.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)C1=CC(C(C)(C)C2CC(C)(C)c3cc4c(cc3C2(C)C)Cc2cc3c(cc2-4)C(C)(C)CCC3(C)C)C=C1
Reaction #358173
light yellow solid
収率 43.3%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CCC(C)(C)c2cc3c(cc21)Cc1cc2c(cc1-3)C(C)(C)CC(C(C)(C)C1C=CC=C1)C2(C)C
Reaction #358174
powder
収率 68.1%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CCC(C)(C)c2cc3c(cc21)Cc1cc2c(cc1-3)C(C)(C)CC(C(C)(C)C1C=CC([Si](C)(C)C)=C1)C2(C)C
Reaction #358175
white solid
収率 93.8%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CCC(C)(C)c2cc3c(cc21)Cc1cc2c(cc1-3)C(C)(C)CC(C(c1ccccc1)(c1ccccc1)C1C=CC(c3ccccc3)=C1)C2(C)C
Reaction #358199
opaque white solid
収率 69.1%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CCC(C)(C)c2cc3c(cc21)Cc1cc2c(cc1-3)C(C)(C)CC(C(c1ccccc1)(c1ccccc1)C1C=CC=C1)C2(C)C
Reaction #358200
powder
収率 79.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CCC(C)(C)c2cc3c(cc21)Cc1cc2c(cc1-3)C(C)(C)CC(C(c1ccccc1)(c1ccccc1)C1C=CC([Si](C)(C)C)=C1)C2(C)C
Reaction #358201
light yellow amorphous product
収率 61.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1cc2c(cc1-c1ccccc1)Cc1cc(-c3ccccc3)c(C(C)(C)C)cc1-2
Reaction #507205
2,7-diphenyl-3,6-di-t-butyl-fluorene
収率 179.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1ccc2c(c1)-c1cc(C(C)(C)C)c(CCl)cc1C2
Reaction #507206
2-chloromethyl-3,6-di-t-butylfluorene
DOI: 10.6084/m9.figshare.5104873.v1
CCC(c1c2c(cc(C(C)(C)C)c1-c1ccccc1)-c1cc(C(C)(C)C)c(-c3ccccc3)cc1C2)C1C=CC=C1
Reaction #507207
(Cyclopentadienyl)-[(2,7-di-phenyl-3,6-di-tert-butylfluorenyl)]-propane
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CCC(C)(C)c2cc3c(cc21)Cc1cc2c(cc1-3)C(C)(C)CCC2(C)C
Reaction #582913
powder
収率 53.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)C1=CC(C(C)(C)C2CC(C)(C)c3cc4c(cc3C2(C)C)Cc2cc3c(cc2-4)C(C)(C)CCC3(C)C)C=C1
Reaction #582914
light yellow solid
収率 43.3%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CCC(C)(C)c2cc3c(cc21)Cc1cc2c(cc1-3)C(C)(C)CC(C(C)(C)C1C=CC=C1)C2(C)C
Reaction #582915
powder
収率 68.1%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CCC(C)(C)c2cc3c(cc21)Cc1cc2c(cc1-3)C(C)(C)CC(C(C)(C)C1C=CC([Si](C)(C)C)=C1)C2(C)C
Reaction #582916
white solid
収率 93.8%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CCC(C)(C)c2cc3c(cc21)Cc1cc2c(cc1-3)C(C)(C)CC(C(c1ccccc1)(c1ccccc1)C1C=CC(c3ccccc3)=C1)C2(C)C
Reaction #582939
opaque white solid
収率 69.1%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CCC(C)(C)c2cc3c(cc21)Cc1cc2c(cc1-3)C(C)(C)CC(C(c1ccccc1)(c1ccccc1)C1C=CC=C1)C2(C)C
Reaction #582940
powder
収率 79.0%DOI: 10.6084/m9.figshare.5104873.v1
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