2-iodoadenosine

[NH4+].[OH-]
Reaction #558544
NH4OH
Rendimiento 0.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_01
Nc1nc(C#CCOc2ccccc2-c2ccccc2)nc2c1ncn2[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O
Reaction #654851
compound 10
Rendimiento 38.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_01
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
Rendimiento 55.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_08
N#CCCCCCC#Cc1nc(N)c2ncn([C@@H]3O[C@H](CO)[C@@H](O)[C@H]3O)c2n1
Reaction #673306
above-titled compound
Rendimiento 199.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_08
N#CCCCCC#Cc1nc(N)c2ncn([C@@H]3O[C@H](CO)[C@@H](O)[C@H]3O)c2n1
Reaction #806267
2-(6-cyano-1-hexyn-1-yl)adenosine
Rendimiento 55.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_11
CO[C@@H]1[C@H](O)[C@@H](CO)O[C@H]1n1cnc2c(N)nc(I)nc21
Reaction #811982
Compound 47
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_01
Nc1nc(C#CCC2CCN(C(=O)Oc3ccccc3)CC2)nc2c1ncn2[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O
Reaction #820084
2-{3-[1-(Phenoxycarbonyl)piperidin-4-yl]propyn-1-yl}adenosine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_09
Nc1nc(C#CCC2CCN(C(=O)Oc3ccc(F)cc3)CC2)nc2c1ncn2[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O
Reaction #820085
2-{3-[1-((4-Fluorophenoxy)carbonyl)piperidin-4-yl]propyn-1-yl}adenosine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_09
Nc1nc(C#CCC2CCN(C(=O)Oc3ccc([N+](=O)[O-])cc3)CC2)nc2c1ncn2[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O
Reaction #820086
2-{3-[1-((4-Nitrophenoxy)carbonyl)piperidin-4-yl]propyn-1-yl}adenosine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_09
COC(=O)c1ccc(OC(=O)N2CCC(CC#Cc3nc(N)c4ncn([C@@H]5O[C@H](CO)[C@@H](O)[C@H]5O)c4n3)CC2)cc1
Reaction #820087
2-{3-[1-((4-Methoxycarbonylphenoxy)carbonyl)piperidin-4-yl]propyn-1-yl}adenosine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_09
Nc1nc(C#CCC2CCN(C(=O)Oc3ccc(Cl)cc3)CC2)nc2c1ncn2[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O
Reaction #820088
2-{3-[1-((4-Chloro)phenoxycarbanoyl)piperidin-4-yl]propyn-1-yl}adenosine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_09
COc1ccc(OC(=O)N2CCC(CC#Cc3nc(N)c4ncn([C@@H]5O[C@H](CO)[C@@H](O)[C@H]5O)c4n3)CC2)cc1
Reaction #820089
2-{3-[1-((4-Methoxy)phenoxycarbanoyl)piperidin-4-yl]propyn-1-yl}adenosine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_09
Cc1ccc(OC(=O)N2CCC(CC#Cc3nc(N)c4ncn([C@@H]5O[C@H](CO)[C@@H](O)[C@H]5O)c4n3)CC2)cc1
Reaction #820090
2-{3-[1-((4-Methyl)phenoxycarbanoyl)piperidin-4-yl]propyn-1-yl}adenosine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_09
Nc1nc(C#CCC2CCN(C(=O)OCc3ccc([N+](=O)[O-])cc3)CC2)nc2c1ncn2[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O
Reaction #820091
2-{3-[1-((4-Nitro)benzyloxycarbanoyl)piperidin-4-yl]propyn-1-yl}adenosine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_09
Nc1nc(C#CCC2CCN(C(=O)Oc3ccccc3Cl)CC2)nc2c1ncn2[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O
Reaction #820092
2-{3-[1-((2-Chloro)phenoxycarbanoyl)piperidin-4-yl]propyn-1-yl}adenosine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_09
Cc1ccc(OC(=O)N2CCC(CC#Cc3nc(N)c4ncn([C@@H]5O[C@H](CO)[C@@H](O)[C@H]5O)c4n3)CC2)cc1C
Reaction #820093
2-{3-[1-((3,4-Dimethyl)phenoxycarbanoyl)piperidin-4-yl]propyn-1-yl}adenosine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_09
Nc1nc(C#CCC2CCN(C(=O)Oc3ccc(F)c(F)c3)CC2)nc2c1ncn2[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O
Reaction #820094
2-{3-[1-((3,4-Difluoro)phenoxycarbanoyl)piperidin-4-yl]propyn-1-yl}adenosine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_09
CNC1(N)N=C(I)N=C2C1=NCN2[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O
Reaction #942680
2-iodo-6-methylamino adenosine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_08
CO[C@H]1[C@@H](O)[C@H](n2cnc3c(N)nc(I)nc32)O[C@@H]1CO
Reaction #1052512
Compound 48
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_06
Nc1ncnc2c1ncn2[C@]1(C#CCC2CCN(C(=O)Oc3ccccc3Cl)CC2)O[C@H](CO)[C@@H](O)[C@H]1O
Reaction #1102146
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_07
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