5-Bromoindan-1-one

COC(=O)C1Cc2cc(Br)ccc2C1=O
Reaction #9374
5-bromo-1-oxo-indan-2-carboxylic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COC(=O)C1Cc2cc(Br)ccc2C1=O
Reaction #57016
5-bromo-1-oxo-indan-2-carboxylic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
Brc1ccc2c(c1)CC=C2
Reaction #70956
6-bromo-1H-indene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CC1(C)CCC(NC2CCc3cc(Br)ccc32)CC1
Reaction #157488
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=C1CCc2cc(N3CCN(c4cccnc4)C3=O)ccc21
Reaction #167217
1-(1-oxo-indan-5-yl)-3-pyridin-3-yl-imidazolidin-2-one
Ausbeute 61.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
N#Cc1ccc2c(c1)CCC2=O
Reaction #190363
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Brc1ccc2c(c1)CCC21OCCO1
Reaction #195000
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Brc1ccc2c(c1)CCC2=NOCc1ccccc1
Reaction #205290
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C1NCCc2cc(Br)ccc21
Reaction #226298
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
OC1(C2SCCCS2)CCc2cc(Br)ccc21
Reaction #234134
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Brc1ccc2c(c1)CC=C2
Reaction #238244
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
OC1CCc2cc(Br)ccc21
Reaction #260617
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CON=C1CCc2cc(Br)ccc21
Reaction #285047
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CC(C)(C)[C@H]1CC[C@H](NC2CCc3cc(Br)ccc32)CC1
Reaction #317203
(5-Bromo-2,3-dihydro-1H-inden-1-yl)(trans-4-tert-butylcyclohexyl)amine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
O=C1Nc2ccccc2C1=C1CCc2cc(Br)ccc21
Reaction #372700
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
OC1CCc2cc(Br)ccc21
Reaction #387809
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
O=C1CCc2cc(-c3cccs3)ccc21
Reaction #390515
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
O=C1CCc2cc(-c3ccc(OCc4ccccc4)cc3)ccc21
Reaction #391107
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
ON=C1CCc2cc(Br)ccc21
Reaction #392533
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
OC1CCc2cc(Br)ccc21
Reaction #394126
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
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