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239581

C[C@@]1(O)[C@H](O)[C@@H](CO)O[C@H]1n1cc(Cl)c2c(NO)ncnc21
Reaction #59241
123
DOI: 10.6084/m9.figshare.5104873.v1
C=Cc1cn(C2OC(CO)C(O)C2(C)O)c2ncnc(NO)c12
Reaction #59243
2-(4-Hydroxyamino-5-vinyl-pyrrolo[2,3-d]pyrimidin-7-yl)-5-hydroxymethyl-3-methyl-tetrahydro-furan-3,4-diol
DOI: 10.6084/m9.figshare.5104873.v1
CC1(O)C(O)C(CO)OC1n1cc(-c2cnco2)c2c(Cl)ncnc21
Reaction #59244
2-(4-Chloro-5-oxazol-5-yl-pyrrolo[2,3-d]pyrimidin-7-yl)-5-hydroxymethyl-3-methyl-tetrahydro-furan-3,4-diol
DOI: 10.6084/m9.figshare.5104873.v1
CC1(O)C(O)C(CO[Si](C)(C)C(C)(C)C)OC1n1ccc2c(N)ncnc21
Reaction #203312
DOI: 10.1039/C8SC04228D
C=Cc1cn(C2OC(CO)C(O)C2(C)O)c2ncnc(NO)c12
Reaction #250032
DOI: 10.1039/C8SC04228D
CC1(O)C(O)C(CO)OC1n1cc(Cl)c2c(N)ncnc21
Reaction #253197
DOI: 10.1039/C8SC04228D
CC1(O)C(O)C(CO)OC1n1cc(C=O)c2c(NN)ncnc21
Reaction #380652
DOI: 10.1039/C8SC04228D
CC1(O)C(O)C(CO)OC1n1c(N)nc2c(N)ncnc21
Reaction #381617
DOI: 10.1039/C8SC04228D
C[C@@]1(O)[C@H](O)[C@@H](CO)O[C@H]1n1ccc2c(Cl)ncnc21
Reaction #535854
desired compound
Ausbeute 65.6%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@]1(O)[C@H](O)[C@@H](CO)O[C@H]1n1cc(Cl)c2c(N)ncnc21
Reaction #535872
desired product
Ausbeute 35.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@]1(O)[C@H](O)[C@@H](CO)O[C@H]1n1cc(Br)c2c(N)ncnc21
Reaction #535873
desired product
Ausbeute 36.2%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cn([C@@H]2O[C@H](CO)[C@@H](O)[C@@]2(C)O)c2ncnc(Cl)c12
Reaction #535880
desired compound
Ausbeute 77.9%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cn([C@@H]2O[C@H](CO)[C@@H](O)[C@@]2(C)O)c2ncnc(N)c12
Reaction #535881
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@]1(O)[C@H](O)[C@@H](CO)O[C@H]1n1c(Br)nc2c(N)ncnc21
Reaction #535893
desired product
Ausbeute 21.1%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@]1(O)[C@H](O)[C@@H](CO)O[C@H]1n1cc(F)c2c(N)ncnc21
Reaction #535899
desired product
DOI: 10.6084/m9.figshare.5104873.v1
C#Cc1cn([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O)c2ncnc(N)c12
Reaction #720960
title compound 2o
Ausbeute 96.2%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ncnc2c1c(-c1c[nH]nn1)cn2[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O
Reaction #720961
title compound 2p
Ausbeute 24.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@]1(O)[C@H](O)[C@@H](CO)O[C@H]1n1cc(I)c2c(N)ncnc21
Reaction #720966
title compound 6
Ausbeute 69.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@]1(O)[C@H](O)[C@@H](CO)O[C@H]1n1cc(-c2ccccc2)c2c(N)ncnc21
Reaction #720967
title compound 7a
Ausbeute 70.2%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@]1(O)[C@H](O)[C@@H](CO)O[C@H]1n1cnc2c(N)nnnc21
Reaction #800901
2′-C-methyl-2-azaadenosine
DOI: 10.6084/m9.figshare.5104873.v1
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