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O=CCc1cccc(Br)c1
Reaction #1301
(3-bromophenyl)acetaldehyde
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CCC(=O)c2cc(Br)ccc21
Reaction #1309
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CCC(Br)c2cc(Br)ccc21
Reaction #1310
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CCC(OC2CCCCC2)c2cc(Br)ccc21
Reaction #1311
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C#Cc1ccc2c(c1)C(=O)CCC2(C)C
Reaction #1313
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CCC(Br)c2cc(Br)ccc21
Reaction #1316
Compound I
DOI: 10.6084/m9.figshare.5104873.v1
CC(=S)C1CCC(C)(C)c2ccc(Br)cc21
Reaction #1317
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=CCc1cccc(Br)c1
Reaction #1451
(3-bromophenyl)acetaldehyde
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CC=C(Sc2ccccc2)c2cc(Br)ccc21
Reaction #1453
4,4-dimethyl-7-bromo-1-phenylthio-3,4-dihydronaphthalene
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)C1=CCC(C)(C)c2ccc(Br)cc21
Reaction #1457
7-bromo-1-(1,1-dimethylethyl)-3,4-dihydro-4,4-dimethylnaphthalene
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CCC(=O)c2cc(Br)ccc21
Reaction #1463
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc(/C=C/c2cccc3c2C(Sc2ccccc2)=CCC3(C)C)cc1
Reaction #1466
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CC=C(Sc2ccccc2)c2cc(Br)ccc21
Reaction #1470
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCSC1=CCC(C)(C)c2ccc(Br)cc21
Reaction #1471
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)C1=CCC(C)(C)c2ccc(Br)cc21
Reaction #1477
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CC1(O)CCC(C)(C)c2ccc(Br)cc21
Reaction #1494
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCc1cc2c(cc1Br)CCCCC2(C)C
Reaction #1733
2-bromo-3-hexyl-5,5-dimethyl-6,7,8,9-tetrahydro-5H-benzocycloheptene
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCc1cc2c(cc1C(=O)O)CCCCC2(C)C
Reaction #1734
3-hexyl-5,5-dimethyl-6,7,8,9-tetrahydro-5H-benzocycloheptene-2-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(C2=CCC(C)(C)c3ccc(Br)cc32)cc1
Reaction #2700
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(C2=CCC(C)(C)c3ccc(Br)cc32)s1
Reaction #2704
title compound
Ausbeute 62.3%DOI: 10.6084/m9.figshare.5104873.v1
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