1,1,1-Trifluoroacetone

CC(O)(COc1ccc(C(=O)c2ccccc2)cc1)C(F)(F)F
Reaction #64157
title compound
Ausbeute 13.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
CC(O)(COc1ccc(S(=O)(=O)c2ccccc2)cc1)C(F)(F)F
Reaction #64158
title compound
Ausbeute 9.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
CC(O)(CSc1ccc(S(=O)(=O)c2ccccc2)cc1)C(F)(F)F
Reaction #64159
title compound
Ausbeute 31.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
CC(O)(C#Cc1ccc(S(=O)(=O)c2ccccc2)cc1)C(F)(F)F
Reaction #64163
butyne
Ausbeute 75.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
CC(O)(C#Cc1ccc(C(=O)c2ccccc2)cc1)C(F)(F)F
Reaction #64164
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
CC(O)(C#Cc1ccc(S(=O)(=O)c2ccncc2)cc1)C(F)(F)F
Reaction #64166
title compound
Ausbeute 50.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
CC(O)(C#Cc1ccc(C(=O)c2ccccn2)cc1)C(F)(F)F
Reaction #64172
title compound
Ausbeute 1.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
CC(=NN=c1[nH]cccc1Cl)C(F)(F)F
Reaction #90226
product
Ausbeute 66.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CC(O)(C#Cc1ccc(C(=O)c2ccccn2)cc1)C(F)(F)F
Reaction #197171
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1ccc(CN=C(C)C(F)(F)F)cc1
Reaction #207405
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(O)(c1ccc(Br)cc1)C(F)(F)F
Reaction #221342
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COc1cc(F)c(C(C)(O)C(F)(F)F)c(F)c1
Reaction #222733
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(=CC(=O)OCc1ccccc1)C(F)(F)F
Reaction #244142
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(C)(C)OC(=O)NCC#CC(C)(O)C(F)(F)F
Reaction #251015
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(O)(c1nc2cc([N+](=O)[O-])ccc2s1)C(F)(F)F
Reaction #262133
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
O=C(C=CC=CC=Cc1ccccc1)C(F)(F)F
Reaction #265151
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COC(=O)C1(C(O[Si](C)(C)C(C)(C)C)C2CCCCC2)NC(=O)C(CCCl)C12CO2
Reaction #294275
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COc1ccc(C(C)(O)C(F)(F)F)cc1
Reaction #300354
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CC(=CC(=O)OCc1ccccc1)C(F)(F)F
Reaction #303534
benzyl 4,4,4-trifluoro-3-methylbut-2-enoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
COc1cc(F)c(C(C)(O)C(F)(F)F)c(F)c1
Reaction #317777
title compound
Ausbeute 78.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
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