Teilstruktursuche

C1CC(OC1)CO

Nc1nc(O)c2ncn(COC(CO)CO)c2n1
Reaction #3723
ganciclovir
DOI: 10.6084/m9.figshare.5104873.v1
Nc1ncnc2c1ncn2[C@H]1C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O)OP(=O)(O)O)O1
Reaction #4349
dATP
DOI: 10.6084/m9.figshare.5104873.v1
COC[C@H]1O[C@@H](n2cnc3c(NC4CCCC4)ncnc32)[C@H](O)[C@@H]1O
Reaction #6761
N6-cyclopentyl-5′-O-methyladenosine
DOI: 10.6084/m9.figshare.5104873.v1
COC[C@H]1O[C@@H](n2cnc3c(NCc4cccc(I)c4)ncnc32)[C@H](O)[C@@H]1O
Reaction #6762
N6-(3-iodobenzyl)-5′-O-methyladenosine
DOI: 10.6084/m9.figshare.5104873.v1
CCOC[C@H]1O[C@@H](n2cnc3c(NC4CCCC4)ncnc32)[C@H](O)[C@@H]1O
Reaction #6765
N6-cyclopentyl-5′-O-ethyladenosine
DOI: 10.6084/m9.figshare.5104873.v1
CCOC[C@H]1O[C@@H](n2cnc3c(NCc4cccc(I)c4)ncnc32)[C@H](O)[C@@H]1O
Reaction #6766
N6-(3-Iodobenzyl)-5′-O-Ethyladenosine
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #6880
material
Ausbeute 88.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #6881
material
Ausbeute 71.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1nc(OCC2CC2)c2sc(=O)n([C@@H]3O[C@H](CO)[C@@H](O)[C@H]3O)c2n1
Reaction #47757
63
Ausbeute 29.3%DOI: 10.6084/m9.figshare.5104873.v1
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.v1
CC(=O)Nc1ncc2sc(=O)n([C@@H]3O[C@H](COC(C)=O)[C@@H](OC(C)=O)[C@H]3OC(C)=O)c2n1
Reaction #47765
82
Ausbeute 90.2%DOI: 10.6084/m9.figshare.5104873.v1
O=c1[nH]cnc2c([C@@H]3O[C@H](CO)[C@@H](O)[C@H]3O)n[nH]c12
Reaction #55227
formycin B
DOI: 10.6084/m9.figshare.5104873.v1
O=c1[nH]c(=O)n([C@H]2C[C@H](O)[C@@H](CO)O2)cc1C#CCOc1ccc([N+](=O)[O-])cc1
Reaction #56622
5-[3-(4-Nitrophenoxy)-1-propynyl]-2′-deoxyuridine
DOI: 10.6084/m9.figshare.5104873.v1
CCC(=O)c1c(Cl)n([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O)c2cc(Cl)c(Cl)cc12
Reaction #56623
2,5,6-trichloro-3-propionyl-1-(β-D-ribofuranosyl)indole
DOI: 10.6084/m9.figshare.5104873.v1
CNc1c(C=O)c2cc(Cl)c(Cl)cc2n1[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O
Reaction #56624
4.18
Ausbeute 43.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)Nc1c(C=O)c2cc(Cl)c(Cl)cc2n1[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O
Reaction #56625
4.19
Ausbeute 83.8%DOI: 10.6084/m9.figshare.5104873.v1
COc1c(C=O)c2cc(Cl)c(Cl)cc2n1[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O
Reaction #56626
4.25
Ausbeute 42.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1c(C#N)c2cc(Cl)c(Cl)cc2n1[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O
Reaction #56627
4.26
Ausbeute 67.5%DOI: 10.6084/m9.figshare.5104873.v1
OC[C@H]1O[C@@H](N2c3cc(Cl)c(Cl)cc3C(=C=NO)C2Cl)[C@H](O)[C@@H]1O
Reaction #56628
4.29
Ausbeute 70.0%DOI: 10.6084/m9.figshare.5104873.v1
CON=C=C1c2cc(Cl)c(Cl)cc2N([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O)C1Cl
Reaction #56629
4.30
Ausbeute 41.0%DOI: 10.6084/m9.figshare.5104873.v1
Seite 1Weiter