4-bromostyrene

CCOC(=O)C1CC(c2ccc(Br)cc2)c2c(Cl)cc(Cl)cc2N1
Reaction #75671
Compound 39
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
O=C(O)C1CC(c2ccc(Br)cc2)c2c(Cl)cc(Cl)cc2N1
Reaction #75672
Compound 40
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
CCOC(=O)C1CC(c2ccc(Br)cc2)c2cc(Cl)ccc2N1
Reaction #75688
Compound 56
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
O=C(O)C1CC1c1ccc(Br)cc1
Reaction #246232
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
C=Cc1ccc(-c2c3ccccc3nc3ccccc23)cc1
Reaction #346534
9-(p-vinylphenyl)acridine
Ausbeute 42.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1977_07
C=Cc1ccc(C(O)(C(F)(F)F)C(F)(F)F)cc1
Reaction #484436
4-(Hexafluorohydroxyisopropyl)styrene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_08
BrC=Cc1ccccc1.C=C(C)C(=O)[O-].C=CC=O
Reaction #578433
bromostyrene acrolein methacrylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_05
Brc1ccc(C=Cc2ccc(Br)cc2)cc1
Reaction #591322
4,4′-Dibromostilbene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_08
C=Cc1ccc([C@H]2C[C@]3(C)C(=O)CC[C@H]3[C@@H]3CC[C@@]4(O)CC5(CCC4=C32)OCC(C)(C)CO5)cc1
Reaction #639237
title compound
Ausbeute 62.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_05
C=Cc1ccc([C@H]2C[C@]3(C)C(=O)CC[C@H]3[C@@H]3CC[C@@]4(O)CC5(CCC4=C32)OCC(C)(C)CO5)cc1
Reaction #642407
title compound
Ausbeute 62.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_11
O=S(=O)(c1ccccc1)N1CC1c1ccc(Br)cc1
Reaction #647264
1-benzenesulfonyl-2-(4-bromo-phenyl)-aziridine
Ausbeute 48.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_11
C=Cc1ccc(B(O)O)cc1
Reaction #670829
solid
Ausbeute 93.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_07
CCC[P+](CC)(CC)CC.[I-]
Reaction #683740
triethyl n-propyl phosphonium iodide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1977_03
C=Cc1ccc([C@H]2C[C@]3(C)C(=O)CC[C@H]3[C@@H]3CC[C@@]4(O)CC5(CCC4=C32)OCC(C)(C)CO5)cc1
Reaction #687363
title compound
Ausbeute 62.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_03
C=Cc1ccc(C(=O)C(=O)OCCc2ccccc2)cc1
Reaction #717752
desired compound
Ausbeute 68.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_04
C=Cc1ccc(C(=O)C(=O)OC/C=C(\C)CCC=C(C)C)cc1
Reaction #717753
oil
Ausbeute 21.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_04
C=Cc1ccc(C(=O)C(=O)OCC/C=C\CC)cc1
Reaction #717755
oil
Ausbeute 50.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_04
C=Cc1ccc(C(=O)C(=O)O[C@@H]2C[C@H](C)CC[C@H]2C(C)C)cc1
Reaction #717757
oil
Ausbeute 47.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_04
N#CC=Cc1ccc(C=Cc2ccc(Br)cc2)cc1
Reaction #763838
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
C=Cc1ccc(P(c2ccccc2)c2ccccc2)cc1
Reaction #816396
(4-vinylphenyl)diphenylphosphine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_09
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