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CCOC(=O)Cc1ccc(N)cc1F

CC(C)(C)OC(=O)C1(c2ccc([N+](=O)[O-])cc2F)CC1
Reaction #175519
DOI: 10.1039/C8SC04228D
CCOC(=O)Cc1cc(Cl)c(NC(=O)c2cn(C)c3cc(F)ccc23)cc1F
Reaction #182833
DOI: 10.1039/C8SC04228D
CCOC(=O)Cc1ccc(N2C(=O)c3c(c(OCC)c4ccccc4c3OCC)C2O)cc1F
Reaction #203424
DOI: 10.1039/C8SC04228D
CCOC(=O)C(C(=O)OCC)c1cc(F)c([N+](=O)[O-])cc1F
Reaction #206182
DOI: 10.1039/C8SC04228D
Cn1cc(C(=O)Nc2cc(F)c(CC(=O)O)cc2Cl)c2cc(F)ccc21
Reaction #210061
DOI: 10.1039/C8SC04228D
CCOC(=O)C(c1ccc(N)cc1F)c1cc(C)c(C(=O)c2ccccc2)n1C
Reaction #212193
DOI: 10.1039/C8SC04228D
O=C(O)Cc1cc(Cl)c(NC(=O)c2nccc3ccccc23)cc1F
Reaction #226482
DOI: 10.1039/C8SC04228D
COc1cc(C#N)cc(Oc2c([N+](=O)[O-])ccc(C(C(=O)OC(C)(C)C)C(=O)OC(C)(C)C)c2F)c1
Reaction #228152
DOI: 10.1039/C8SC04228D
CCOC(=O)Cc1ccc(Cl)c(Oc2cc(Cl)cc(Br)c2)c1F
Reaction #231901
DOI: 10.1039/C8SC04228D
CCOC(=O)Cc1ccc(NC(=O)c2cc(OCc3cccc(Cl)c3)ccc2Cl)cc1F
Reaction #266012
DOI: 10.1039/C8SC04228D
CCOC(=O)Cc1cc(Cl)c(NC(=O)c2cn(C)c3ccc(F)cc23)cc1F
Reaction #271723
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)C(C(=O)OC(C)(C)C)c1ccc([N+](=O)[O-])c(Oc2cccc3ccccc23)c1F
Reaction #271738
DOI: 10.1039/C8SC04228D
CCCCCCCCCCCCCCCCNc1ccc(CC(=O)O)c(F)c1
Reaction #272366
DOI: 10.1039/C8SC04228D
CCOC(=O)C(CC(C)C)(C(=O)OCC)c1cc(F)c([N+](=O)[O-])cc1F
Reaction #292679
DOI: 10.1039/C8SC04228D
CCOC(=O)Cc1ccc(N)cc1F
Reaction #309606
title compound
Ausbeute 60.3%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(=O)c1cc(CO[Si](c2ccccc2)(c2ccccc2)C(C)(C)C)c(N2C[C@@H](C)O[C@@H](C)C2)c(F)c1F
Reaction #332593
title compound
Ausbeute 81.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(=O)c1cc(CO[Si](c2ccccc2)(c2ccccc2)C(C)(C)C)c(N2C[C@@H](C)O[C@H](C)C2)c(F)c1F
Reaction #332594
Ethyl 2-(5-((tert-butyldiphenylsilyloxy)methyl)-4-((2R,6R)-2,6-dimethylmorpholino)-2,3-difluorophenyl)-2-oxoacetate
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CN(c2c(CO[Si](c3ccccc3)(c3ccccc3)C(C)(C)C)cc(C(=O)C(=O)O)c(F)c2F)C[C@H](C)O1
Reaction #332596
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(=NO)c1cc(CO[Si](c2ccccc2)(c2ccccc2)C(C)(C)C)c(N2C[C@@H](C)O[C@@H](C)C2)c(F)c1F
Reaction #332630
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1noc2c(F)c(N3C[C@@H](C)O[C@@H](C)C3)c(CO[Si](c3ccccc3)(c3ccccc3)C(C)(C)C)cc12
Reaction #332633
title compound
Ausbeute 66.6%DOI: 10.6084/m9.figshare.5104873.v1
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