(4S,5R)-4-(3,5-difluorobenzyl)-5-((2R,4R)-4-(allyloxy)pyrrolidin-2-yl)oxazolidin-2-one

C=CCO[C@@H]1C[C@H]([C@@H](O)[C@@H](N)Cc2cc(F)cc(F)c2)N(C(c2ccccc2)c2ccccc2)C1
Reaction #49213
title compound
Ausbeute 87.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=C1N[C@@H](Cc2cc(F)cc(F)c2)[C@@H]([C@H]2C[C@H](O)CN2C(c2ccccc2)c2ccccc2)O1
Reaction #49217
title compound
Ausbeute 95.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=C1N[C@@H](Cc2cc(F)cc(F)c2)[C@@H]([C@H]2C[C@@H](O)CN2C(c2ccccc2)c2ccccc2)O1
Reaction #220122
title compound
Ausbeute 87.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
O=C1N[C@@H](Cc2cc(F)cc(F)c2)[C@@H]([C@H]2C[C@H](O)CN2C(c2ccccc2)c2ccccc2)O1
Reaction #220128
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
C=CCO[C@@H]1C[C@H]([C@@H](O)[C@@H](N)Cc2cc(F)cc(F)c2)N(C(c2ccccc2)c2ccccc2)C1
Reaction #1102040
title compound
Ausbeute 87.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_07
O=C1N[C@@H](Cc2cc(F)cc(F)c2)[C@@H]([C@H]2C[C@H](O)CN2C(c2ccccc2)c2ccccc2)O1
Reaction #1102044
title compound
Ausbeute 95.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_07