1-bromo-3-methylbut-2-ene

CC(C)=CCSc1ccccc1Br
Reaction #51269
2-bromo-1-(3-methylbut-2-enylthio)benzene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
COc1cccc(SCC=C(C)C)c1
Reaction #51272
expected compound
Ausbeute 90.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CC(C)=CCCc1cc(Cl)nc(Cl)n1
Reaction #51471
2,4-dichloro-6-(4-methyl-3-pentenyl)pyrimidine
Ausbeute 74.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
C/C=C/COC(C)C1=CC(C)(C)Nc2ccc(-c3ccccc3OC)cc21
Reaction #54068
title compound
Ausbeute 32.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
COc1cccc([C@@]23CCCC[C@@H]2C(=O)N(CC=C(C)C)C(=O)C3)c1
Reaction #54756
N-(3,3-dimethylallyl)-4a-(m-methoxyphenyl)-1,3-diketo-cis-decahydroisoquinoline
Ausbeute 94.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_04
COc1ccc(OCC=C(C)C)c(C=O)c1
Reaction #58371
5-methoxy-2-(3 -methylbut-2-enyloxy)benzaldehyde
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CC(C)=CCSc1ccc(Br)cc1
Reaction #64641
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
CC(C)=CCSc1cccc(Br)c1
Reaction #65682
m-bromophenyl 3-methyl-2-butenyl sulfide
Ausbeute 98.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
CC(C)=CCn1ccnc1[N+](=O)[O-]
Reaction #75434
N-(Dimethylallyl)-2-nitroimidazole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
CC(C)=CCn1cc(C)nc1[N+](=O)[O-]
Reaction #75442
1-(4-methyl-2-nitro-1H-imidazol-1-yl)-3-methyl-2-butene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
CC(C)=CCN1CC[C@H]2[C@@H](C1)c1cc(Nc3cccc(C(F)(F)F)c3F)cc3c1N2CCOC3
Reaction #75849
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
CC(C)=CCOc1cc([N+](=O)[O-])ccc1Cl
Reaction #78290
1-chloro-2-(3-methyl-2-butenyloxy)-4-nitrobenzene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
CC(C)=CCn1c(Cl)nc2c1c(=O)[nH]c(=O)n2C
Reaction #181957
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1cccc2c1nc(-c1c(F)cccc1F)n2CC=C(C)C
Reaction #182788
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)=CCSc1ccc(Br)cc1
Reaction #185650
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOS(=O)(=O)C(CC=C(C)C)c1ccccc1
Reaction #195432
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC(=O)C(C)(C)CC=C(C)C
Reaction #204866
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)=CCC(C#N)(C#N)CC(F)(F)C(F)(F)C(F)(F)C(F)F
Reaction #207088
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC(=O)c1nc(Br)n(CC=C(C)C)c1C(=O)OC
Reaction #211696
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)=CCCC(=O)OC(C)(C)C
Reaction #216969
title compound
Ausbeute 82.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_11
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