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Nc1ncnc2c1ncn2[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O
Reaction #3749
Adenosine
DOI: 10.6084/m9.figshare.5104873.v1
CCNC(=O)C1OC(n2cnc3c(N)nc(C#CC4(O)CCCCC4C)nc32)C(O)C1O
Reaction #44344
5-[6-Amino-2-(1-hydroxy-2-methyl-cyclohexylethynyl)-purin-9-yl]-3,4-dihydroxytetrahydrofuran-2-carboxylic acid ethylamide
المردود 65.0%DOI: 10.6084/m9.figshare.5104873.v1
CCNC(=O)C1OC(n2cnc3c(N)nc(C#CC4(O)CCCC(C)C4)nc32)C(O)C1O
Reaction #44345
5-[6-Amino-2-(1-hydroxy-3-methyl-cyclohexylethynyl)-purin-9-yl]-3,4-dihydroxytetrahydrofuran-2-carboxylic acid ethylamide
DOI: 10.6084/m9.figshare.5104873.v1
Clc1nc(N[C@H]2CC[C@H](Nc3nc(Cl)nc4c3ncn4C3CCCCO3)CC2)c2ncn(C3CCCCO3)c2n1
Reaction #44901
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Nc1ncnc2c1ncn2[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O
Reaction #50344
Adenosine
DOI: 10.6084/m9.figshare.5104873.v1
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.v1
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.v1
CCOC(=O)C(O)[C@H]1O[C@@H](n2cnc3c(N)ncnc32)[C@H](O)[C@@H]1O
Reaction #56253
adenosine-5'-carboxylic acid ethyl ester
المردود 78.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCOC(=O)C(O)[C@H]1O[C@@H](n2cnc3c(N)ncnc32)[C@H](O)[C@@H]1O
Reaction #56255
crude product
المردود 87.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ncnc2c1ncn2[C@@H]1O[C@H](C(O)C(=O)OCc2ccccc2)[C@@H](O)[C@H]1O
Reaction #56257
Adenosine-5'-carboxylic acid benzyl ester
DOI: 10.6084/m9.figshare.5104873.v1
NNC(=O)C(O)[C@H]1O[C@@H](n2cnc3c(N)ncnc32)[C@H](O)[C@@H]1O
Reaction #56259
adenosine-5'-carboxylic acid hydrazide
المردود 93.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)NC(=O)C(O)[C@H]1O[C@@H](n2cnc3c(N)ncnc32)[C@H](O)[C@@H]1O
Reaction #56260
adenosine-5'-carboxylic acid N-tert.-butylamide
المردود 38.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)OC2C(CO)OC(n3cnc4c(N)ncnc43)C2O1
Reaction #58780
2′,3′-Isopropylidene-adenosine
DOI: 10.6084/m9.figshare.5104873.v1
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.v1
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.v1
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.v1
Nc1ncnc2c1ncn2C1OC(CF)C(O)C1O
Reaction #252134
DOI: 10.1039/C8SC04228D
CCCSCC1OC(n2cnc3c(N)ncnc32)C(O)C1O
Reaction #262805
DOI: 10.1039/C8SC04228D
Nc1ncnc2c1nc(C(F)(F)F)n2C1OC(CO)C(O)C1O
Reaction #271637
DOI: 10.1039/C8SC04228D
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.v1
الصفحة 1التالي