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OCCF

N#Cc1ccc(OC(F)F)cc1
Reaction #3113
title compound
Ausbeute 41.0%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccc(OC(F)F)cc1
Reaction #3114
title compound
Ausbeute 73.4%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(OC(F)F)cc1
Reaction #3115
title compound
Ausbeute 53.2%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccc(OC(F)F)cc1
Reaction #3116
title compound
Ausbeute 65.0%DOI: 10.6084/m9.figshare.5104873.v1
O=Cc1ccc(OC(F)F)c(O)c1
Reaction #3117
title compound
Ausbeute 38.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N1CCc2cc(OC(F)F)c(Br)cc21
Reaction #3118
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCO[Si](OCC)(OCC)OC(=O)C(F)(F)Cl
Reaction #12079
chlorodifluoroacetic acid, triethoxysilyl ester
DOI: 10.6084/m9.figshare.5104873.v1
FC(F)Oc1ccc(Br)nc1
Reaction #43322
title compound
Ausbeute 43.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CC[C@@H](OCCF)C1
Reaction #43355
title compound
Ausbeute 41.0%DOI: 10.6084/m9.figshare.5104873.v1
OCCN1CC[C@@H](OCCF)C1
Reaction #43356
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCCc1nn(-c2cc([N+](=O)[O-])ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(C)(C)C)cc1
Reaction #64556
title compound
Ausbeute 37.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCc1nn(-c2cc([N+](=O)[O-])ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(C)(C)C)cc1F
Reaction #64578
title compound
Ausbeute 62.0%DOI: 10.6084/m9.figshare.5104873.v1
FC(F)Oc1cccnc1Cl
Reaction #67630
2-chloro-3-(difluoromethoxy)pyridine
Ausbeute 72.0%DOI: 10.6084/m9.figshare.5104873.v1
FC(F)Oc1cnc2c(NCc3nnc4ccc(-c5ccccc5)nn34)ccnc2c1
Reaction #68538
title compound
Ausbeute 17.7%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(-c2ccc3nnc(COc4ccnc5cc(OC(F)F)ccc45)n3c2)on1
Reaction #68611
7-(difluoromethoxy)-4-((6-(3-methylisoxazol-5-yl)-[1,2,4]triazolo[4,3-a]pyridin-3-yl)methoxy)quinoline
Ausbeute 13.4%DOI: 10.6084/m9.figshare.5104873.v1
FC(F)Oc1cnc2c(Cl)ccnc2c1
Reaction #68647
8-chloro-3-(difluoromethoxy)-1,5-naphthyridine
Ausbeute 56.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(=O)C(OCCF)C1
Reaction #71975
title compound
Ausbeute 97.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CC[C@H](NCc2ccccc2)[C@H](OCCF)C1
Reaction #71976
title compound
Ausbeute 77.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)c1ccc2ccccc2n1
Reaction #80823
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(C)C1CCc2cc(Br)cc3[nH]c(=O)c(=O)n1c23
Reaction #80824
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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