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89465

CC1=CCC(C(C)(C)C)=C1
Reaction #358164
light yellow liquid
Ausbeute 23815.2%DOI: 10.6084/m9.figshare.5104873.v1
CC1=CC(C(C)(C)C)=CC1=C(C)C
Reaction #358165
yellow liquid
DOI: 10.6084/m9.figshare.5104873.v1
C=C1C(C)=C(C)C(C)=C1C(C)(C)C
Reaction #498290
t-butyl-trimethyl-fulvene
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=CCC(C(C)(C)C)=C1
Reaction #582905
light yellow liquid
Ausbeute 23815.2%DOI: 10.6084/m9.figshare.5104873.v1
CC1=CC(C(C)(C)C)=CC1=C(C)C
Reaction #582906
yellow liquid
DOI: 10.6084/m9.figshare.5104873.v1
CC1=CC(C(C)(C)C2=CC3=C(CCCCC3)C2)c2ccccc21
Reaction #704604
2-[1-(3-methyl-1H-Inden-1-yl) -1-methyl-ethyl]-1,4,5,6,7,8-hexahydroazulene
Ausbeute 67.3%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)C2=C(C=C3N=c4ccccc4=C31)C(c1ccc(N(c3ccccc3)c3ccccc3)cc1)=C1C=CC(c3ccccc3)C=C12
Reaction #806230
12,12-dimethyl-10-phenyl-7-(4-diphenylamino-phenyl)-10,12-dihydroindeno[2,1-b]carbazole
Ausbeute 58.4%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)C2=C(C=C3N=c4ccccc4=C31)C(c1ccc(N(c3ccccc3)c3ccc(-c4ccccc4)cc3)cc1)=C1C=CC(c3ccccc3)C=C12
Reaction #806231
7-[4-{(biphenyl-4-yl)-phenylamino}-phenyl]-12,12-dimethyl-10-phenyl-10,12-dihydroindeno[2,1-b]carbazole
Ausbeute 116.2%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)C2=C(C=C3N=c4ccccc4=C31)C(c1ccc(N(c3ccc(-c4ccccc4)cc3)c3ccc(-c4ccccc4)cc3)cc1)=C1C=CC(c3ccccc3)C=C12
Reaction #806232
7-[4-{bis(biphenyl-4-yl)amino}-phenyl]-12,12-dimethyl-10-phenyl-10,12-dihydroindeno[2,1-b]carbazole
Ausbeute 143.2%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)C2=C(C=C3N=c4ccccc4=C31)C(c1ccc3c(c1)c1ccccc1n3-c1ccccc1)=C1C=CC(c3ccc(-c4ccccc4)cc3)C=C12
Reaction #806235
10-(biphenyl-4-yl)-12,12-dimethyl-7-(9-phenyl-9H-carbazol-3-yl)-10,12-dihydroindeno[2,1-b]carbazole
Ausbeute 45.2%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)C2=C(C=C3N=c4ccccc4=C31)C(c1ccc(N(c3ccc(-c4ccccc4)cc3)c3ccc(-c4ccccc4)cc3)cc1)=C1C=CC(c3ccc(-c4ccccc4)cc3)C=C12
Reaction #806236
10-(biphenyl-4-yl)-7-[4-bis(biphenyl-4-yl)amino-phenyl]-12,12-dimethyl-10,12-dihydroindeno[2,1-b]carbazole
Ausbeute 63.8%DOI: 10.6084/m9.figshare.5104873.v1
CC1=CC(C(C)(C)C)=CC1=C(C)c1ccccc1
Reaction #1448744
red orange liquid
Ausbeute 241.5%DOI: 10.6084/m9.figshare.5104873.v1
CC1=CCC(C(C)(C)C)=C1
Reaction #1523533
light-yellow liquid
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 #1729190
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 #1729191
desired product
Ausbeute 153.4%DOI: 10.6084/m9.figshare.5104873.v1
CC1=CCC(C(C)(C)C)=C1
Reaction #2000773
light yellow liquid
DOI: 10.6084/m9.figshare.5104873.v1
CC1=CC(C(C)(C)C)=CC1=C(C)C
Reaction #2000774
yellow liquid
DOI: 10.6084/m9.figshare.5104873.v1
CC1=C2C=C(C(C)(C)C)C=C2C(C)(C)C1
Reaction #2044991
5-tert-butyl-1,1,3-trimethyl-1,2-dihydropentalene
DOI: 10.6084/m9.figshare.5104873.v1
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