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1269727

CC1(C)OC2C(CNC3CC(CCC(=O)OCc4ccccc4)C3)OC(n3cnc4c(N)ncnc43)C2O1
Reaction #273903
DOI: 10.1039/C8SC04228D
COc1ccc(CNc2ncnc3c2ccn3C2OC(CNC3CC(CCC(=O)OCc4ccccc4)C3)C3OC(C)(C)OC32)c(OC)c1
Reaction #294253
DOI: 10.1039/C8SC04228D
CC1(C)O[C@@H]2[C@H](O1)[C@@H](CNC1CC(CCC(=O)OCc3ccccc3)C1)O[C@H]2n1cnc2c(N)ncnc21
Reaction #598854
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)O[C@@H]2[C@H](O1)[C@@H](CNC1CC(CCC(=O)OCc3ccccc3)C1)O[C@H]2n1cnc2c(N)ncnc21
Reaction #598858
product
Ausbeute 61.6%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CNc2ncnc3c2ccn3[C@@H]2O[C@H](CNC3CC(CCC(=O)OCc4ccccc4)C3)[C@H]3OC(C)(C)O[C@H]32)c(OC)c1
Reaction #598867
desired compound
Ausbeute 71.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C1CC2(C1)CC(C(=O)OCc1ccccc1)C2
Reaction #607559
benzyl 6-oxospiro[3.3]heptane-2-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)OC2C(CNC3CC(CCC(=O)OCc4ccccc4)C3)OC(n3cnc4c(N)ncnc43)C2O1
Reaction #777529
DOI: 10.1039/C8SC04228D
O=C1CC(CCC(=O)OCc2ccccc2)C1
Reaction #794852
9
Ausbeute 93.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CCC1CC(=O)C1
Reaction #794853
10
Ausbeute 99.4%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CNc2ncnc3c2ccn3C2OC(CNC3CC(CCC(=O)OCc4ccccc4)C3)C3OC(C)(C)OC32)c(OC)c1
Reaction #1639103
DOI: 10.1039/C8SC04228D
CC1(C)O[C@@H]2[C@H](O1)[C@@H](CNC1CC(CCC(=O)OCc3ccccc3)C1)O[C@H]2n1cnc2c(N)ncnc21
Reaction #2127892
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)O[C@@H]2[C@H](O1)[C@@H](CNC1CC(CCC(=O)OCc3ccccc3)C1)O[C@H]2n1cnc2c(N)ncnc21
Reaction #2127896
product
Ausbeute 61.6%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CNc2ncnc3c2ccn3[C@@H]2O[C@H](CNC3CC(CCC(=O)OCc4ccccc4)C3)[C@H]3OC(C)(C)O[C@H]32)c(OC)c1
Reaction #2127905
desired compound
Ausbeute 71.2%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CNc2ncnc3c2ccn3[C@@H]2O[C@H](CNC3CC(CCC(=O)OCc4ccccc4)C3)[C@H]3OC(C)(C)O[C@H]32)c(OC)c1
Reaction #2127912
desired compound
Ausbeute 64.0%DOI: 10.6084/m9.figshare.5104873.v1