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8628

C[C@H](O)[C@H](NC(=O)OC(C)(C)C)c1cc(F)c(F)c(F)c1
Reaction #44601
title compound
Ausbeute 86.3%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](OC(=O)c1ccc([N+](=O)[O-])cc1)[C@H](NC(=O)OC(C)(C)C)c1cc(F)c(F)c(F)c1
Reaction #44602
title compound
Ausbeute 76.4%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](O)[C@H](NC(=O)OC(C)(C)C)c1cc(F)c(F)c(F)c1
Reaction #44603
title compound
Ausbeute 95.1%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](O)[C@H](N)c1cc(F)c(F)c(F)c1.Cl
Reaction #44604
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](O[Si](c1ccccc1)(c1ccccc1)C(C)(C)C)[C@H](NC(=O)OC(C)(C)C)c1cc(F)c(F)c(F)c1
Reaction #44607
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](OC(=O)c1ccc([N+](=O)[O-])cc1)[C@H](NC(=O)OC(C)(C)C)c1cc(F)c(F)c(F)c1
Reaction #44633
title compound
Ausbeute 76.4%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](O)[C@H](NC(=O)OC(C)(C)C)c1cc(F)c(F)c(F)c1
Reaction #44634
title compound
Ausbeute 95.1%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](O[Si](c1ccccc1)(c1ccccc1)C(C)(C)C)[C@H](NC(=O)OC(C)(C)C)c1cc(F)c(F)c(F)c1
Reaction #44635
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](O)[C@H]1COC[C@@H](c2cc(F)c(F)c(F)c2)N1C(=O)OCc1ccccc1
Reaction #44666
titled compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)[C@H]1COC[C@@H](c2cc(F)c(F)c(F)c2)N1C(=O)OCc1ccccc1
Reaction #44667
titled compound
Ausbeute 91.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)[C@H]1COC[C@@H](c2cc(F)c(F)c(F)c2)N1
Reaction #44668
titled compound
Ausbeute 100.3%DOI: 10.6084/m9.figshare.5104873.v1
CCN(Cc1ccccc1)C(=O)OCc1cc(C(F)(F)F)ccc1-c1cc(CC(=O)OC)ccc1F
Reaction #66978
{2′-[(Benzyl-ethyl-carbamoyloxy)-methyl]-6-fluoro-4′-trifluoromethyl-biphenyl-3-yl}-acetic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1noc(Cc2ccc(F)c(F)c2F)n1
Reaction #86927
ethyl 5-(2,3,4-trifluorobenzyl)-1,2,4-oxadiazole-3-carboxylate
Ausbeute 12.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCc2cc(F)c(F)cc21
Reaction #157454
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)NCc1cc(F)c(Nc2cc(OC(C)C)[nH]n2)nc1N[C@@H](CO)c1ccc(F)cc1
Reaction #163053
title compound
Ausbeute 39.0%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cc(CC(=O)O)ccc1F
Reaction #169371
title compound
Ausbeute 65.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)Cc1ccc(F)c(C#N)c1
Reaction #169372
title compound
Ausbeute 87.0%DOI: 10.6084/m9.figshare.5104873.v1
CSc1ccc(OC(F)(F)C(OS(=O)(=O)C(F)(F)F)c2ccc(F)cc2)cc1
Reaction #174561
DOI: 10.1039/C8SC04228D
COc1cc2c(cc1F)OCC21C(=O)N(Cc2ccc(C(F)(F)F)o2)c2ccccc21
Reaction #176883
DOI: 10.1039/C8SC04228D
O=CC(c1ccc(F)cc1)c1ccc(F)cc1
Reaction #182307
DOI: 10.1039/C8SC04228D
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