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Nc1ncnc2c1ncn2[C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]1O
Reaction #2055
5'-AMP
DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2ccccc2C(=O)N1c1ncnc2c1ncn2O
Reaction #6348
title compound
収率 83.5%DOI: 10.6084/m9.figshare.5104873.v1
CCOC[C@H]1O[C@@H](n2cnc3c(NCc4cccc(I)c4)nc(Cl)nc32)[C@H](O)[C@@H]1O
Reaction #6768
N6-(3-iodobenzyl)-2-Chloro-5′-O-ethyladenosine
DOI: 10.6084/m9.figshare.5104873.v1
Nc1nc(NC2CC2)c2ncn([C@@H]3O[C@H](CO)[C@@H](O)[C@H]3F)c2n1
Reaction #65349
title compound
DOI: 10.6084/m9.figshare.5104873.v1
c1nc(NC2CC2)c2nc[nH]c2n1
Reaction #65352
cream solid
収率 153.1%DOI: 10.6084/m9.figshare.5104873.v1
OC[C@H]1O[C@@H](n2cnc3c(NC4CC4)ncnc32)[C@H](F)[C@@H]1O
Reaction #65353
title compound
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #65356
hydrate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](n2cnc3c(NC(=O)c4ccccc4)ncnc32)C[C@@H]1O
Reaction #83830
N6 -benzoyl-5'-O-tert-butyldimethylsilyl-2'-deoxyadenosine
収率 76.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ncc(-c2nc(N3CCOCC3)c3nc(N4CCOCC4)n(CC4CCOC4)c3n2)cn1
Reaction #174489
DOI: 10.1039/C8SC04228D
COC(=O)Cc1cccc(Cn2cnc3c(N)nc(Cl)nc32)c1
Reaction #174834
DOI: 10.1039/C8SC04228D
CCCCNc1nc(N)c2nc[nH]c2n1
Reaction #178192
DOI: 10.1039/C8SC04228D
CC(C)OP(=O)(C=CCCOn1cnc2c(N3C(=O)c4ccccc4C3=O)ncnc21)OC(C)C
Reaction #184687
DOI: 10.1039/C8SC04228D
Cc1nc2ccccc2n1-c1nc(N2CCOCC2)c2nc(CN3CC4CC3CO4)n(C)c2n1
Reaction #186628
DOI: 10.1039/C8SC04228D
Fc1nc(NCc2ccncc2)c2nc[nH]c2n1
Reaction #190490
DOI: 10.1039/C8SC04228D
Nc1nc(OCc2ccc(CNC(=O)C(F)(F)F)cc2)c2nc[nH]c2n1
Reaction #193745
DOI: 10.1039/C8SC04228D
COC(=O)c1cccc(Cn2cnc3c(N)nc(Cl)nc32)c1
Reaction #195920
DOI: 10.1039/C8SC04228D
C[Si](C)(C)CCOCn1cnc2nc(N3CCOCC3)nc(N3CCOCC3)c21
Reaction #196643
DOI: 10.1039/C8SC04228D
OCC1CCCN1c1nc(-n2cnc3ccccc32)c2nc[nH]c2n1
Reaction #199955
DOI: 10.1039/C8SC04228D
CCCC(C)Oc1nc(N)c2nc(OC)n(CCCCNC3CCOC3)c2n1
Reaction #207985
DOI: 10.1039/C8SC04228D
NCCCn1cnc2c(N)ncnc21
Reaction #211055
DOI: 10.1039/C8SC04228D
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