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487786

CC(C)N(CC1OC(n2cnc3c(N)ncnc32)C2OC(C)(C)OC12)C1CC(CCC(=O)O)C1
Reaction #231424
DOI: 10.1039/C8SC04228D
CCOC(=O)CCC1CC(N(CC2OC(n3cnc4c(N)ncnc43)C3OC(C)(C)OC23)C(C)C)C1
Reaction #241128
DOI: 10.1039/C8SC04228D
CCOC(=O)CCC1CC(N(C[C@H]2O[C@@H](n3cnc4c(N)ncnc43)[C@@H]3OC(C)(C)O[C@@H]32)C(C)C)C1
Reaction #598757
title compound
Ausbeute 15.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)N(C[C@H]1O[C@@H](n2cnc3c(N)ncnc32)[C@@H]2OC(C)(C)O[C@@H]21)C1CC(CCC(=O)OCc2ccccc2)C1
Reaction #598855
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)N(C[C@H]1O[C@@H](n2cnc3c(N)ncnc32)[C@@H]2OC(C)(C)O[C@@H]21)C1CC(CCC(=O)O)C1
Reaction #598856
3-[3-({[(3aR,4R,6R,6aR)-6-(6-amino-9H-purin-9-yl)-2,2-dimethyl-tetrahydro-2H-furo[3,4-d][1,3]dioxol-4-yl]methyl}(propan-2-yl)amino)cyclobutyl]propanoic acid
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)N(CC1OC(n2cnc3c(N)ncnc32)C2OC(C)(C)OC12)C1CC(CCC(=O)OCc2ccccc2)C1
Reaction #916539
DOI: 10.1039/C8SC04228D
CCOC(=O)CCC1CC(N(C[C@H]2O[C@@H](n3cnc4c(N)ncnc43)[C@@H]3OC(C)(C)O[C@@H]32)C(C)C)C1
Reaction #2127798
title compound
Ausbeute 15.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)N(C[C@H]1O[C@@H](n2cnc3c(N)ncnc32)[C@@H]2OC(C)(C)O[C@@H]21)C1CC(CCC(=O)OCc2ccccc2)C1
Reaction #2127893
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)N(C[C@H]1O[C@@H](n2cnc3c(N)ncnc32)[C@@H]2OC(C)(C)O[C@@H]21)C1CC(CCC(=O)O)C1
Reaction #2127894
3-[3-({[(3aR,4R,6R,6aR)-6-(6-amino-9H-purin-9-yl)-2,2-dimethyl-tetrahydro-2H-furo[3,4-d][1,3]dioxol-4-yl]methyl}(propan-2-yl)amino)cyclobutyl]propanoic acid
DOI: 10.6084/m9.figshare.5104873.v1