An 14 Reaktionen beteiligt

1219247

O=C(NC(CC(F)(F)F)C(=O)O)OCc1ccccc1
Reaction #172067
2-(benzyloxycarbonylamino)-4,4,4-trifluorobutanoic acid
Ausbeute 20.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
COC(=O)c1cn(C(=O)OC(C)(C)C)c2nccc(CNC(CC(F)(F)F)C(=O)O)c12
Reaction #179554
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
NC(CO)CC(F)(F)F
Reaction #914194
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
NC(CO)CC(F)(F)F
Reaction #1452732
2-amino-4,4,4-trifluorobutan-1-ol
Ausbeute 53.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_02
O=C(OCc1ccccc1)C(O)CC(F)(F)F
Reaction #1473969
desired product
Ausbeute 25.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_07
O=C(O)C(O)CC(F)(F)F
Reaction #1573944
12-2
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_08
NC(CO)CC(F)(F)F
Reaction #1681508
2-amino-4,4,4-trifluoro-butan-1-ol
Ausbeute 38.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_11
COC(=O)c1cn(C(=O)OC(C)(C)C)c2nccc(CN[C@H](CC(F)(F)F)C(=O)O)c12
Reaction #1714310
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_07
CCOC(=O)C([NH3+])CC(F)(F)F.[Cl-]
Reaction #1752014
1-Ethoxy-4,4,4-trifluoro-1-oxobutan-2-aminium chloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_10
COC(=O)c1cn(C(=O)OC(C)(C)C)c2nccc(CN[C@H](CC(F)(F)F)C(=O)O)c12
Reaction #2055406
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_04
NC(CO)CC(F)(F)F
Reaction #2073160
2-amino-4,4,4-trifluoro-butan-1-ol
Ausbeute 38.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_06
NC(CO)CC(F)(F)F
Reaction #2242284
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (4/10)
O=C(NC(CC(F)(F)F)C(=O)O)OCc1ccccc1
Reaction #2288299
2-(benzyloxycarbonylamino)-4,4,4-trifluorobutanoic acid
Ausbeute 20.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_06
NC(CO)CC(F)(F)F
Reaction #2354104
2-amino-4,4,4-trifluoro-butan-1-ol
Ausbeute 38.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_12