An 10 Reaktionen beteiligt

721543

CC(=O)Nc1nc(OS(=O)(=O)c2c(C(C)C)cc(C(C)C)cc2C(C)C)c2sc(=O)n([C@@H]3O[C@H](COC(C)=O)[C@@H](OC(C)=O)[C@H]3OC(C)=O)c2n1
Reaction #47752
5-acetylamino-7-(2,4,6-triisopropyl-benzenesulfonyloxy)-3-(2′,3′,5′-tri-O-acetyl-β-D-ribofuranosyl)thiazolo[4,5-d]pyrimidin-2-one
Ausbeute 92.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(=O)Nc1nc(OC(C)C)c2sc(=O)n([C@@H]3O[C@H](COC(C)=O)[C@@H](OC(C)=O)[C@H]3OC(C)=O)c2n1
Reaction #47754
27
Ausbeute 65.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(=O)Nc1nc(Cl)c2sc(=O)n([C@@H]3O[C@H](COC(C)=O)[C@@H](OC(C)=O)[C@H]3OC(C)=O)c2n1
Reaction #47764
81
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(=O)Nc1nc(OS(=O)(=O)c2c(C(C)C)cc(C(C)C)cc2C(C)C)c2sc(=O)n([C@@H]3O[C@H](COC(C)=O)[C@@H](OC(C)=O)[C@H]3OC(C)=O)c2n1
Reaction #636967
5-acetylamino-7-(2,4,6-triisopropyl-benzenesulfonyloxy)-3-(2′,3′,5′-tri-O-acetyl-β-D-ribofuranosyl)thiazolo[4,5-d]pyrimidin-2-one
Ausbeute 92.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_05
CC(=O)Nc1nc(OC(C)C)c2sc(=O)n([C@@H]3O[C@H](COC(C)=O)[C@@H](OC(C)=O)[C@H]3OC(C)=O)c2n1
Reaction #636969
27
Ausbeute 65.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_05
CC(=O)Nc1nc(Cl)c2sc(=O)n([C@@H]3O[C@H](COC(C)=O)[C@@H](OC(C)=O)[C@H]3OC(C)=O)c2n1
Reaction #636979
81
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_05
CC(=O)Nc1nc(OS(=O)(=O)c2c(C(C)C)cc(C(C)C)cc2C(C)C)c2sc(=O)n([C@@H]3O[C@H](COC(C)=O)[C@@H](OC(C)=O)[C@H]3OC(C)=O)c2n1
Reaction #670926
5-acetylamino-7-(2,4,6-triisopropyl-benzenesulfonyloxy)-3-(2′,3′,5′-tri-O-acetyl-β-D-ribofuranosyl)thiazolo[4,5-d ]pyrimidin-2-one
Ausbeute 92.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_08
CC(=O)Nc1nc(OS(=O)(=O)c2c(C(C)C)cc(C(C)C)cc2C(C)C)c2sc(=O)n([C@@H]3O[C@H](COC(C)=O)[C@@H](OC(C)=O)[C@H]3OC(C)=O)c2n1
Reaction #2339579
5-acetylamino-7-(2,4,6-triisopropyl-benzenesulfonyloxy)-3-(2′,3′,5′-tri-O-acetyl-β-D-ribofuranosyl)thiazolo [4,5-d]pyrimidin-2-one
Ausbeute 92.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_01
CC(=O)Nc1nc(OC(C)C)c2sc(=O)n([C@@H]3O[C@H](COC(C)=O)[C@@H](OC(C)=O)[C@H]3OC(C)=O)c2n1
Reaction #2339581
27
Ausbeute 65.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_01
CC(=O)Nc1nc(Cl)c2sc(=O)n([C@@H]3O[C@H](COC(C)=O)[C@@H](OC(C)=O)[C@H]3OC(C)=O)c2n1
Reaction #2339590
81
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_01