Selectfluor

Cc1c(F)sc2ccccc12
Reaction #10325
2-fluoro-3-methyl-1-benzothiophene
Ausbeute 72.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COc1nc(C(=O)CF)c(NC(=O)OC(C)(C)C)cc1F
Reaction #43409
1,1-Dimethylethyl [5-fluoro-2-(fluoroacetyl)-6-(methyloxy)-3-pyridinyl]carbamate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COc1ccc2c(N)c(F)c(=O)oc2c1OC1CCCC1
Reaction #48920
4-amino-8-(cyclopentyloxy)-3-fluoro-7-methoxy-2H-chromen-2-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COC(=O)c1cc(Br)cc2c1c(F)cn2C(C)C
Reaction #70809
methyl 6-bromo-3-fluoro-1-isopropyl-1H-indole-4-carboxylate
Ausbeute 20.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
COc1cc(OC)c(F)c(-c2ccc(Br)c3nccnc23)c1
Reaction #71394
5-bromo-8-(2-fluoro-3,5-dimethoxy-phenyl)-quinoxaline
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CCOC(=O)c1ccc(-c2cc(OC)cc(OC)c2F)c2nccnc12
Reaction #71455
title compound
Ausbeute 46.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
Fc1cc2cc(Br)ccc2o1
Reaction #73904
5-Bromo-2-fluoro-1-benzofuran
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CCN(C(=O)OC(C)(C)C)[C@H]1CCN(c2c(F)cnc3c2c2cc(C#N)ncc2n3COCC[Si](C)(C)C)C1
Reaction #88557
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
COC(=O)c1cc(Br)cc2c1c(F)cn2C(C)C
Reaction #90708
methyl 6-bromo-3-fluoro-1-isopropyl-1H-indole-4-carboxylate
Ausbeute 20.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
COc1ccc2c(c1F)CCCC2=O
Reaction #91368
title compound
Ausbeute 42.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CCOC(=O)C1(F)CCCn2c(-c3ccc(-c4cnc(C)o4)c(OC)c3)nnc21
Reaction #158328
title compound
Ausbeute 60.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC1CN(C(=O)C(F)(F)F)CCc2cc(F)c(Cl)cc21
Reaction #171307
white solid
Ausbeute 60.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCOP(=O)(OCC)OC[C@H](CCCCNC(=O)[C@@H](NC(=O)OC)C(c1ccccc1)c1ccccc1)N(CC(C)C)S(=O)(=O)c1ccc(N)c(F)c1
Reaction #219883
white solid
Ausbeute 48.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
CC1CN(C(=O)C(F)(F)F)CCc2cc(F)c(Cl)cc21
Reaction #308473
white solid
Ausbeute 60.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
Fc1c[nH]c2ncnc(Cl)c12
Reaction #309349
title compound
Ausbeute 36.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
Cc1c(C(=O)N[C@H](c2cccc(F)c2)C2CCC2)c(C)n(-c2ccccc2)c(=O)c1F
Reaction #309984
crude title product
Ausbeute 19.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
COC(=O)Cc1cc(O)c2cc(F)ccc2c1F
Reaction #325796
(1,6-difluoro-4-hydroxy-naphthalen-2-yl)acetic acid methyl ester
Ausbeute 86.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
COC(=O)Cc1c(F)c(O)c2cc(F)ccc2c1Br
Reaction #325801
(1-bromo-3,6-difluoro-4-hydroxy-naphthalen-2-yl)-acetic acid methyl ester
Ausbeute 42.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
O=[N+]([O-])c1cc(Br)cc2[nH]nc(F)c12.O=[N+]([O-])c1cc(Br)cc2[nH]ncc12
Reaction #331827
title compound
Ausbeute 49.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
CCOC(=O)c1c(F)cnn1C(C)C
Reaction #331838
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
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