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C=C(C)C(=C)C

COC(=O)c1ccc2c(c1)C(=CCN1CCN(C)CC1)c1ccccc1CO2
Reaction #5138
methyl 11-[2-(4-methyl-1-piperazinyl)ethylidene]-6,11-dihydrodibenz[b,e]oxepin-2-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
C=C1CC2CCC(C)(O2)C1=C
Reaction #10997
product
Ausbeute 94.3%DOI: 10.6084/m9.figshare.5104873.v1
CC1=C(C)C(c2ccccc2CO)C(C)=C1C
Reaction #43975
2-(2,3,4,5-tetramethylcyclopentadienyl)benzylalcohol
Ausbeute 97.7%DOI: 10.6084/m9.figshare.5104873.v1
CC1=C(C)C(c2ccccc2C[O][Ti+2])C(C)=C1C.C[N-]C.C[N-]C
Reaction #43977
2-(2,3,4,5-tetramethylcyclopentadienyl)benzyloxytitanium bis(dimethylamide)
Ausbeute 83.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)[Si](C(C)C)(C(C)C)N1C=C2C=C(F)OCC3=C2C(=C1)CC3N(C)C
Reaction #53615
titled compound
DOI: 10.6084/m9.figshare.5104873.v1
CSC1=CC2=CN([Si](C(C)C)(C(C)C)C(C)C)C=C3CC(N(C)C)C(=C23)CO1
Reaction #53616
titled compound
Ausbeute 69.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)[Si](C(C)C)(C(C)C)N1C=C2C=C(C=O)OCC3=C2C(=C1)CC3N(C)C
Reaction #53617
titled compound
Ausbeute 59.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1C(Br)=CC=C2C1=Cc1ccccc12
Reaction #53765
yellow solid
Ausbeute 92.9%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)C1(O)CC=C2C[C@@H]3[C@@H]4C=C[C@H](O)[C@@H]5OC1=C2[C@]45CCN3C
Reaction #82145
3-acetylmorphine
Ausbeute 80.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1CC[C@]23C4=C5O[C@H]2[C@@H](O)C=C[C@H]3[C@H]1CC4=CCC5(O)[Si](C)(C)C(C)(C)C
Reaction #82146
product
Ausbeute 56.1%DOI: 10.6084/m9.figshare.5104873.v1
O=C1C(c2cccc(-c3ccccc3)c2)=C(c2ccc(Br)cc2)C(c2ccc(Br)cc2)=C1c1cccc(-c2ccccc2)c1
Reaction #85586
tetraarylcyclopentadienone
Ausbeute 53.1%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #85587
crystals
Ausbeute 40.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1C(c2ccccc2)=C(c2ccccc2)C(c2cc(C#Cc3ccccc3)cc(C#Cc3ccccc3)c2)=C1c1ccccc1
Reaction #217835
4-(3,5-bis(phenylethynyl)phenyl)-2,3,5-triphenylcyclopentadienone
Ausbeute 76.4%DOI: 10.6084/m9.figshare.5104873.v1
O=C1C(c2ccccc2)=C(c2ccccc2)C(c2cc(C#Cc3ccccc3)cc(C#Cc3ccccc3)c2)=C1c1ccccc1
Reaction #217836
4-(3,5-bis(phenylethynyl)-phenyl)-2,3,5-triphenylcyclopentadienone
Ausbeute 85.3%DOI: 10.6084/m9.figshare.5104873.v1
CC1=CC(C)C(C)=C1c1cc(C)cc(C)c1NC(=O)C(C)(C)C
Reaction #222451
DOI: 10.1039/C8SC04228D
CC1=C(C)C(C)C(c2ccccc2C=NNc2ccccc2)=C1C
Reaction #234620
DOI: 10.1039/C8SC04228D
C=CCOc1c(C(C)(C)C)cc(C)cc1[Si](CC)(CC)C1C2=CC(C)(C)CCC2=C2C1=c1ccccc1=CC2(C)C
Reaction #238539
DOI: 10.1039/C8SC04228D
CC(=O)Oc1ccc2c(c1)CCC1=C2CCC2(C)C(=O)CC=C12
Reaction #238568
DOI: 10.1039/C8SC04228D
O=CC(=O)C1=CC=C2C(=Cc3ccccc32)C1=O
Reaction #248629
DOI: 10.1039/C8SC04228D
CC1=C(C)C(C)C(c2ccccc2CNc2cc(C)cc(C)c2)=C1C
Reaction #252893
DOI: 10.1039/C8SC04228D
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