adenosine

Clc1nc(N[C@H]2CC[C@H](Nc3nc(Cl)nc4c3ncn4C3CCCCO3)CC2)c2ncn(C3CCCCO3)c2n1
Reaction #44901
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
C=CCO[C@H]1[C@@H](O)[C@H](n2cnc3c(N)ncnc32)O[C@@H]1CO
Reaction #51519
title compound
المردود 66.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CC(C)(C)[Si](C)(C)C(O)CO[C@H]1[C@@H](O)[C@H](n2cnc3c(N)ncnc32)O[C@@H]1CO
Reaction #51525
3′-O (2-tert-butyldimethylsilylhydroxyethyl)adenosine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CC1(C)OC2C(CO)OC(n3cnc4c(N)ncnc43)C2O1
Reaction #58780
2′,3′-Isopropylidene-adenosine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
Nc1nc2c(ncn2[C@@H]2O[C@H](CO)[C@@H](O)[C@H]2F)c(=O)[nH]1
Reaction #65346
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
O=c1[nH]cnc2c1ncn2[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1F
Reaction #65357
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
Nc1nc2c(ncn2[C@@H]2OC[C@@H](O)[C@@H](O)[C@@]2(O)F)c(=O)[nH]1
Reaction #217754
title compound
المردود 100.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
Nc1nc2c(ncn2[C@@H]2C[C@H](O)[C@@H](CO)S2)c(=O)[nH]1
Reaction #319713
9-(2-deoxy-4-thio-α-D-ribofuranosyl)-2-amino-1,6-dihydro-6-oxopurine
المردود 93.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_01
NC(=O)c1ncn([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O)n1
Reaction #343693
ribavirin
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_11
CCCO[C@@H]1[C@H](O)[C@@H](CO)O[C@H]1n1cnc2c(=O)[nH]c(N)nc21
Reaction #351898
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_07
CCCCCO[C@@H]1[C@H](O)[C@@H](CO)O[C@H]1n1cnc2c(=O)[nH]c(N)nc21
Reaction #351900
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_07
CCCCCCCCCO[C@@H]1[C@H](O)[C@@H](CO)O[C@H]1n1cnc2c(=O)[nH]c(N)nc21
Reaction #351903
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_07
CO[C@@H]1[C@H](O)[C@@H](CO)O[C@H]1n1cnc2c(=O)[nH]c(N)nc21
Reaction #351905
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_07
CCCCCCCCCCCCCCCCCCO[C@@H]1[C@H](O)[C@@H](CO)O[C@H]1n1cnc2c(=O)[nH]c(N)nc21
Reaction #351908
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_07
Nc1nc2c(ncn2[C@@H]2O[C@H](CO)[C@@H](O)[C@H]2OCCCCn2ccnc2)c(=O)[nH]1
Reaction #351911
2'-O-(Imidazol-1-yl)butylguanosine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_07
Nc1ncnc2c1ncn2/C=C1/C[C@H]1CO
Reaction #362910
(R)-(−)-synadenol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_03
CCCO[C@@H]1[C@H](O)[C@@H](CO)O[C@H]1n1cnc2c(=O)[nH]c(N)nc21
Reaction #429095
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_01
CCCCCO[C@@H]1[C@H](O)[C@@H](CO)O[C@H]1n1cnc2c(=O)[nH]c(N)nc21
Reaction #429097
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_01
CCCCCCCCCO[C@@H]1[C@H](O)[C@@H](CO)O[C@H]1n1cnc2c(=O)[nH]c(N)nc21
Reaction #429100
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_01
CO[C@@H]1[C@H](O)[C@@H](CO)O[C@H]1n1cnc2c(=O)[nH]c(N)nc21
Reaction #429102
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_01
الصفحة 1التالي