COPPER(I) BROMIDE

O=C(C(=O)c1cccc(F)c1)c1cccc(F)c1
Reaction #46988
product 20
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Fc1cccc(F)c1-c1cc2c3c(c1)[C@@H]1CNCC[C@@H]1N3CCNC2
Reaction #51546
title compound
Ausbeute 5.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
Fc1cc(Br)ccc1C(F)(F)C(F)(F)F
Reaction #70131
product
Ausbeute 75.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
Fc1cccc(F)c1-c1cc2c3c(c1)[C@@H]1CNCC[C@@H]1N3CCNC2
Reaction #75828
title compound
Ausbeute 5.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
—
Reaction #76388
oil
Ausbeute 96.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
O=C(Nc1ccc(Cl)cc1)c1cccnc1NCC1CCN(c2ccncc2)CC1
Reaction #78127
title compound
Ausbeute 13.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
CC1(C)CCC(=O)c2cc(Br)ccc21
Reaction #81552
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
CC(C)(CC=O)c1ccc(F)cc1
Reaction #82534
3-(4-fluorophenyl)-3-methylbutyraldehyde
Ausbeute 43.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
CC(C)(CC=O)c1ccc(Cl)cc1
Reaction #82543
3-(4-chlorophenyl)-3-methylbutyraldehyde
Ausbeute 38.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
CCc1cc(-c2ccc(Cl)cc2)cc(CC)c1Br
Reaction #159466
4-bromo-4′-chloro-3,5-diethylbiphenyl
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCc1cc(-c2ccc(Cl)cc2)ccc1Br
Reaction #159472
4-bromo-4′-chloro-3-ethylbiphenyl
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cc1cc(-c2ccc(Cl)cc2)ccc1Br
Reaction #159477
4-bromo-4′-chloro-3-methylbiphenyl
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
C[Si](C)(C)C#CCc1ccc(OCc2ccccc2)cc1
Reaction #165039
title compound
Ausbeute 72.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
C#CCc1ccc(COc2ccccn2)cc1
Reaction #165043
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC(=O)OC1CCC2C3CCC4CC(=O)CC(C)C4(C)C3CCC12C
Reaction #177877
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1cc(Br)c(Br)c(C(=O)O)c1
Reaction #179103
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
N#Cc1c(F)cccc1Br
Reaction #183902
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(CCC1OCCO1)c1ccc(Cl)cc1
Reaction #189029
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=[N+]([O-])c1ccc2c(ccn2-c2cccnc2)c1
Reaction #191142
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCc1cn(-c2ncccn2)c2c1C(=O)CC(C)(C)C2
Reaction #194319
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
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