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1187289

Nc1nc(I)nc2c1ncn2[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O
Reaction #44332
6.5
Ausbeute 80.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1nc(I)nc2c1ncn2[C@@H]1O[C@H](C(=O)O)[C@@H](O)[C@H]1O
Reaction #44333
6.8
Ausbeute 85.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OCC1OC(n2cnc3c(NC4CCCC4)nc(I)nc32)C(OC(C)=O)C1OC(C)=O
Reaction #177758
DOI: 10.1039/C8SC04228D
Nc1nc(C#CC2CCCCC2)nc2c1ncn2C1OC(CO)C(O)C1O
Reaction #189708
DOI: 10.1039/C8SC04228D
CC1(C)OC2C(C(=O)O)OC(n3cnc4c(N)nc(I)nc43)C2O1
Reaction #199795
DOI: 10.1039/C8SC04228D
CC(=O)OC[C@H]1O[C@@H](n2cnc3c(NC4CCCC4)nc(I)nc32)[C@H](OC(C)=O)[C@@H]1OC(C)=O
Reaction #217493
(2R,3R,4R,5R)-4-acetyloxy-2-(acetyloxymethyl)-5-[6-(cyclopentylamino)-2-iodopurin-9-yl]oxolan-3-yl acetate
DOI: 10.6084/m9.figshare.5104873.v1
Nc1nc(C#CCC2CCN(C(=O)Oc3ccc([N+](=O)[O-])cc3)CC2)nc2c1ncn2C1OC(CO)C(O)C1O
Reaction #224249
DOI: 10.1039/C8SC04228D
Cc1ccc(OC(=O)N2CCC(CC#Cc3nc(N)c4ncn(C5OC(CO)C(O)C5O)c4n3)CC2)cc1
Reaction #241507
DOI: 10.1039/C8SC04228D
CCCCNc1nc2c(N)nc(I)nc2n1C1OC(CO)C(O)C1O
Reaction #242002
DOI: 10.1039/C8SC04228D
COc1ccccc1OC(=O)N1CCC(CC#Cc2nc(N)c3ncn(C4OC(CO)C(O)C4O)c3n2)CC1
Reaction #245290
DOI: 10.1039/C8SC04228D
C=Cc1nc(N)c2ncn(C3OC(CO)C(O)C3O)c2n1
Reaction #261868
DOI: 10.1039/C8SC04228D
Nc1nc(C#CCC2CCN(C(=O)Oc3ccc(F)c(F)c3)CC2)nc2c1ncn2C1OC(CO)C(O)C1O
Reaction #272565
DOI: 10.1039/C8SC04228D
Nc1nc(C#CCC2CCN(C(=O)Oc3ccc(F)cc3)CC2)nc2c1ncn2C1OC(CO)C(O)C1O
Reaction #295819
DOI: 10.1039/C8SC04228D
Nc1nc(C(F)(F)F)nc2c1ncn2C1OC(CO)C(O)C1O
Reaction #376436
DOI: 10.1039/C8SC04228D
Nc1nc(I)nc2c1ncn2[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O
Reaction #413714
2-iodoadenosine
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1nc(I)nc2c1ncn2[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O
Reaction #517576
6.5
Ausbeute 80.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1nc(I)nc2c1ncn2[C@@H]1O[C@H](C(=O)O)[C@@H](O)[C@H]1O
Reaction #517577
6.8
Ausbeute 85.0%DOI: 10.6084/m9.figshare.5104873.v1
[NH4+].[OH-]
Reaction #558544
NH4OH
Ausbeute 0.1%DOI: 10.6084/m9.figshare.5104873.v1
Nc1nc(C#CCOc2ccccc2-c2ccccc2)nc2c1ncn2[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O
Reaction #654851
compound 10
Ausbeute 38.1%DOI: 10.6084/m9.figshare.5104873.v1
N#CCCCCC#Cc1nc(N)c2ncn([C@@H]3O[C@H](CO)[C@@H](O)[C@H]3O)c2n1
Reaction #673303
2-(6-cyano-1-hexyn-1-yl)adenosine
Ausbeute 55.0%DOI: 10.6084/m9.figshare.5104873.v1
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