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C=CCCC1(C2=CCCC(C)(C)C2)OCCO1

Reaction #54161

1-(3,3-dimethyl-cyclohex-6-en-1-yl)-1,1-ethylenedioxy-pent-4-ene

DOI: 10.6084/m9.figshare.5104873.v1

C=C1C=CCC(C)(C)C1

Reaction #54165

1-Methylene-3,3-dimethyl-cyclohex-5-ene

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

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

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

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

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

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

Ausbeute 75.0%DOI: 10.6084/m9.figshare.5104873.v1

Cc1cc(C2=C(c3cc(C)sc3C)CCC=C2)c(C)s1

Reaction #70957

Ausbeute 25.0%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

CC1=C(C(=O)CC(C)O)C(C)(C)CC=C1

Reaction #74867

DOI: 10.6084/m9.figshare.5104873.v1

C=C(CCC[Si](OCC)(OCC)OCC)C(N)=O

Reaction #83163

Ausbeute 77.0%DOI: 10.6084/m9.figshare.5104873.v1

C=CCC1(O)CCC[C@H](Nc2nc(Cl)ncc2F)C1

Reaction #162189

desired product

DOI: 10.6084/m9.figshare.5104873.v1

CCOC(=O)C=C1CCC[C@H](Nc2nc(Cl)ncc2F)C1

Reaction #162191

Ausbeute 99.8%DOI: 10.6084/m9.figshare.5104873.v1

CCOC(=O)CC1(C[N+](=O)[O-])CCC[C@H](Nc2nc(Cl)ncc2F)C1

Reaction #162192

DOI: 10.6084/m9.figshare.5104873.v1

Clc1cccc(/C=C/[C@H]2CCCN2c2ncnc3[nH]cnc23)c1

Reaction #168581

6-[(R)-2-((E)-2-(3-chlorophenyl)vinyl)pyrrolidin-1-yl]-9H-purine

Ausbeute 16.5%DOI: 10.6084/m9.figshare.5104873.v1

NC(=O)c1cc(F)c(C2=CC(=O)CCC2)nc1Nc1ccc(N2CCOCC2)cc1

Reaction #174479

DOI: 10.1039/C8SC04228D

C=CCON=C(CCC)C1=C(O)CC(c2cc(C)cs2)CC1=O

Reaction #175365

DOI: 10.1039/C8SC04228D

Reaction #175811

DOI: 10.1039/C8SC04228D

CC(C)(C)C(O)C(=Cc1ccc(Cl)cc1)n1cncn1

Reaction #181908

DOI: 10.1039/C8SC04228D

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