3-methylbutan-2-one

CC(C)C(C)(O)c1ccc2c(n1)N1[C@H](C2)CN(C(=O)OC(C)(C)C)C[C@H]1C
Reaction #12049
(4R,9aR)-6-(1-(RS)-Hydroxy-1,2-dimethyl-propyl)-4-methyl-3,4,9,9a-tetrahydro-1H-2,4a,5-triaza-fluorene-2-carboxylic acid tert-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC(C)C(=O)C=Cc1ccco1
Reaction #51721
titled compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
O=C1C2CN(CCc3ccc(Br)cc3)CCN2C(=O)N1c1cc(Cl)cc(Cl)c1
Reaction #78262
7-[2-(4-bromophenyl)ethyl]-2-(3,5-dichlorophenyl)-tetrahydro-imidazo[1,5-a]pyrazine-1,3-dione
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
CC1=Nc2ccc(C(=O)O)cc2C1(C)C
Reaction #89789
desired product
Ausbeute 80.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CC1=Nc2cccc(C(=O)O)c2C1(C)C
Reaction #89790
product
Ausbeute 81.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CC1=Nc2cc(C(=O)O)cc(C(=O)O)c2C1(C)C
Reaction #89791
product
Ausbeute 95.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CC1=Nc2ccc(C(=O)O)cc2C1(C)C
Reaction #89792
desired product
Ausbeute 80.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CC1=Nc2cccc(C(=O)O)c2C1(C)C
Reaction #89793
product
Ausbeute 81.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CC(C)c1ccc([N+](=O)[O-])cn1
Reaction #161261
2-isopropyl-5-nitro-pyridine
Ausbeute 28.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC(C)C(C)(O)c1ccc(I)cc1
Reaction #177287
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=O)C=C(C)C(C)C
Reaction #180299
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)C(C)(O)c1cccc(CN(C)Cc2ccc(C(C)(C)C)cc2)c1
Reaction #189050
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(=NN(C)c1ccc(C(F)(F)F)cn1)C(C)C
Reaction #209540
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
C=C(O[Si](C)(C)C)C(C)C
Reaction #229139
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCOC(=O)CC(=O)C(C)C
Reaction #232213
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CN(C(=O)C(C)(C)c1cc(C(F)(F)F)cc(C(F)(F)F)c1)c1cnc(I)cc1-c1ccccc1Cl
Reaction #254445
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(=O)C(C)(C)SC(F)(F)F
Reaction #290630
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CC(=NN(C)c1cc(C(F)(F)F)cc(C(F)(F)F)n1)C(C)C
Reaction #298628
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COCOc1ccc2c(c1)OC(C)(C)C(C=O)=C2
Reaction #304609
7-(methoxymethoxy)-2,2-dimethyl-2H-chromene-3-carbaldehyde
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
Cc1ccc(C(C(=O)C(C)C)c2ccc(C)cc2)cc1
Reaction #315026
white solid
Ausbeute 79.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
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