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CC(C)(C)C=C

C#Cc1ccc2c(c1)C(C)(C)CN(C1CC1)C2
Reaction #52357
title compound
Ausbeute 94.4%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@]1(c2ccccc2Cl)C=CC(CN2CC(=O)C2)=CC1
Reaction #53483
(R*)-(4-[chlorophenyl)[4-(methoxycarbonyl)phenyl]methyl}azetidin-3-one
DOI: 10.6084/m9.figshare.5104873.v1
CC1=C(/C=C/C(C)=C/C=C/C(C)=C/C=C/C=C(C)/C=C/C=C(C)/C=C/C2=C(C)CCCC2(C)C)C(C)(C)CCC1
Reaction #56547
beta-carotene
Ausbeute 85.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1=C(/C=C/C(C)=C/C=C/C(C)=C/C=C/C=C(C)/C=C/C=C(C)/C=C/C2=C(C)CCCC2(C)C)C(C)(C)CCC1
Reaction #56548
beta-carotene
Ausbeute 75.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1=C(/C=C/C(C)=C/C=C/C(C)=C/C=C/C=C(C)/C=C/C=C(C)/C=C/C2=C(C)CCCC2(C)C)C(C)(C)CCC1
Reaction #56549
beta-carotene
Ausbeute 20.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1=C(/C=C/C(C)=C/C=C/C(C)=C/C=C/C=C(C)/C=C/C=C(C)/C=C/C2=C(C)CCCC2(C)C)C(C)(C)CCC1
Reaction #56550
beta-carotene
Ausbeute 65.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1=C(/C=C/C(C)=C/C=C/C(C)=C/C=C/C=C(C)/C=C/C=C(C)/C=C/C2=C(C)CCCC2(C)C)C(C)(C)CCC1
Reaction #56554
beta-carotene
Ausbeute 60.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1=C(/C=C/C(C)=C/C=C/C(C)=C/C=C/C=C(C)/C=C/C=C(C)/C=C/C2=C(C)CCCC2(C)C)C(C)(C)CCC1
Reaction #56555
beta-carotene
Ausbeute 75.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)C=C(c2ccccc2N2CCNCC2)CC1(C)C
Reaction #60448
title compound
Ausbeute 50.9%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CN1CCN(c2ccccc2C2=CC(C)(C)C(C)(C)C2)CC1
Reaction #60449
1-isobutyl-4-[2-(3,3,4,4-tetramethylcyclopent-1-enyl)phenyl]piperazine
Ausbeute 18.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)C1=CC(=Nc2ccc(CC#N)cc2)C=C(C(C)(C)C)C1=O
Reaction #65009
2,6-di-tertiary-butyl-4-(4'-cyanomethylphenylimino)-2,5-cyclohexadiene-1-one
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1cc(Nc2cccc(OCC(=O)O)c2)cc(C(C)(C)C)c1O
Reaction #65013
3-(3,5-di-tertiary-butyl-4-hydroxyanilino)phenoxyacetic acid
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1cc(Nc2ccc(C=CC(=O)O)cc2)cc(C(C)(C)C)c1O
Reaction #65014
4-(3,5-di-tertiary-butyl-4-hydroxyanilino)cinnamic acid
Ausbeute 19.9%DOI: 10.6084/m9.figshare.5104873.v1
CC1=C(/C=C/C(C)=C\C=C\C(C)=C\C(=O)O)C(C)(C)CCC1
Reaction #71591
9-(Z)-retinoic Acid
DOI: 10.6084/m9.figshare.5104873.v1
O=C(N[C@@H](Cc1ccccc1)C(=O)O)C(CS)CS
Reaction #75213
N-[2-(Mercaptomethyl)-3-mercaptopropanoyl]-L-phenylalanine
DOI: 10.6084/m9.figshare.5104873.v1
O=C(N[C@@H](Cc1ccccc1)C(=O)O)C(CS)CS
Reaction #75419
N-[2-(Mercaptomethyl)-3-mercaptopropanoyl]-L-phenylalanine
DOI: 10.6084/m9.figshare.5104873.v1
C=CC(C)(C)c1[nH]cnc1/C=C1\NC(=O)[C@@H](Cc2ccccc2)NC1=O
Reaction #78915
(+)-phenylahistin
DOI: 10.6084/m9.figshare.5104873.v1
C#Cc1ccc2c(c1)C(C)(C)CN(C1CC1)C2
Reaction #79927
title compound
Ausbeute 94.4%DOI: 10.6084/m9.figshare.5104873.v1
CCC(C)(C)C1=CC(=Cc2ccccc2)C=C(C(C)(C)CC)C1=O
Reaction #81034
title compound
Ausbeute 41.7%DOI: 10.6084/m9.figshare.5104873.v1
CCCCC(=O)O[C@]1(C(=O)C(O)OC(=O)[C@@H](NC(=O)[C@@H]2CCCN2C(=O)[C@H](C)NC(=O)[C@H](C)NC(=O)OC(C)(C)C)C(C)C)[C@@H](C)C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(F)[C@@H](O)C[C@@]21C
Reaction #81348
N-(N-(N-(N-((1,1-dimethyl)ethoxycarbonyl)-L-alanyl) -L-alanyl)-L-prolyl)-L-valine [9α-fluoro-11β,21-dihydroxy-16β-methyl-3,20-dioxo-17-valeroyloxy-pregna-1,4-dien-21-yl ] ester
Ausbeute 63.0%DOI: 10.6084/m9.figshare.5104873.v1
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