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52147

CC1=Cc2cccc(-c3ccccc3)c2C1
Reaction #245149
DOI: 10.1039/C8SC04228D
CC1=Cc2cccc(-c3ccccc3)c2C1
Reaction #444010
3
Ausbeute 90090.4%DOI: 10.6084/m9.figshare.5104873.v1
CC1=Cc2c(-c3ccccc3)cccc2C1CCC1C(C)=Cc2c(-c3ccccc3)cccc21
Reaction #444021
32
Ausbeute 5.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1=Cc2cccc(-c3ccccc3)c2C1
Reaction #569008
compound 13a
DOI: 10.6084/m9.figshare.5104873.v1
CC1=Cc2cccc(-c3ccccc3)c2C1
Reaction #779269
DOI: 10.1039/C8SC04228D
COc1c(C(C)(C)C)cc2c(c1-c1ccccc1)C=C(C)C2[Si](C)(C)C1C(C)=Cc2c(-c3ccccc3)cc(C(C)(C)C)cc21
Reaction #803627
yellowish glassy solid
Ausbeute 72.4%DOI: 10.6084/m9.figshare.5104873.v1
COc1c(C(C)(C)C)cc2c(c1-c1ccccc1)C=C(C)C2[Si](C)(C)C1C(C)=Cc2c(-c3ccc(C(C)(C)C)cc3)cccc21
Reaction #803628
title compound
Ausbeute 91.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1=Cc2c(-c3ccc(C(C)(C)C)cc3)cccc2C1[Si](C)(C)C1C(C)=Cc2c1cc(C(C)C)c(Oc1c(F)c(F)c(F)c(F)c1F)c2-c1ccccc1
Reaction #803633
title product
Ausbeute 53.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1c(C(C)(C)C)cc2c(c1-c1ccc(C(C)(C)C)cc1)C=C(C)C2[Si](C)(C)C1C(C)=Cc2c(-c3ccc(C(C)(C)C)cc3)cccc21
Reaction #803649
title product
Ausbeute 100.4%DOI: 10.6084/m9.figshare.5104873.v1
COc1c(C(C)(C)C)cc2c(c1-c1cc(C(C)(C)C)cc(C(C)(C)C)c1)C=C(C)C2[Si](C)(C)C1C(C)=Cc2c(-c3ccc(C(C)(C)C)cc3)cccc21
Reaction #803653
title product
Ausbeute 80.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1=Cc2c(cccc2-c2cc(C(C)(C)C)cc(C(C)(C)C)c2)C1
Reaction #929637
4-[3′,5′-di-t-butylphenyl]-2-methylindene
DOI: 10.6084/m9.figshare.5104873.v1
CC1=Cc2c(cccc2-c2cc(C(C)(C)C)cc(C(C)(C)C)c2)C1
Reaction #929642
4-[3′,5′-di-t-butylphenyl]-2-methylindene
DOI: 10.6084/m9.figshare.5104873.v1
CC1=Cc2c(cccc2-c2cc(C(C)(C)C)cc(C(C)(C)C)c2)C1
Reaction #929652
4-[3′,5′-di-t-butylphenyl]-2-methylindene
DOI: 10.6084/m9.figshare.5104873.v1
CC1=Cc2c(cccc2-c2cc(C(C)(C)C)cc(C(C)(C)C)c2)C1
Reaction #929662
4-[3′,5′-di-t-butylphenyl]-2-methylindene
DOI: 10.6084/m9.figshare.5104873.v1
CC1=Cc2c(cccc2-c2cc(C(C)(C)C)cc(C(C)(C)C)c2)C1
Reaction #929663
4-(3′,5′-di-t-butylphenyl)-2-methylindene
DOI: 10.6084/m9.figshare.5104873.v1
CC1=Cc2c(cccc2-c2cc(C(C)(C)C)cc(C(C)(C)C)c2)C1
Reaction #929679
4-(3′,5′-di-t-butylphenyl)-2-methylindene
DOI: 10.6084/m9.figshare.5104873.v1
CC1=Cc2c(cccc2-c2cc(C(C)(C)C)cc(C(C)(C)C)c2)C1
Reaction #929691
4-[3′,5′-di-t-butylphenyl]-2-methylindene
DOI: 10.6084/m9.figshare.5104873.v1
CC1=Cc2c(cccc2-c2cc(C(C)(C)C)cc(C(C)(C)C)c2)C1
Reaction #929692
4-(3′,5′-di-t-butylphenyl)-2-methylindene
DOI: 10.6084/m9.figshare.5104873.v1
CC1=Cc2c(cccc2-c2cc(C(C)(C)C)cc(C(C)(C)C)c2)C1
Reaction #929706
4-[3′,5′-di-t-butylphenyl]-2-methylindene
DOI: 10.6084/m9.figshare.5104873.v1
CC1=Cc2c(cccc2-c2cc(C(C)(C)C)cc(C(C)(C)C)c2)C1
Reaction #929707
4-(3′,5′-di-t-butylphenyl)-2-methylindene
DOI: 10.6084/m9.figshare.5104873.v1
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