-
3
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-
1342307286
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M. Roovers, J. Wouters, J. M. Bujnicki, C. Tricot, V. Stalon, H. Grosjean and L. Droogmans, Nucleic Acids Res., 2004, 32, 465.
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Roovers, M.1
Wouters, J.2
Bujnicki, J.M.3
Tricot, C.4
Stalon, V.5
Grosjean, H.6
Droogmans, L.7
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4
-
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0028932657
-
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X. Ariza, V. Bou and J. Vilarrasa, J. Am. Chem. Soc., 1995, 117, 3665.
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(1995)
J. Am. Chem. Soc.
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, pp. 3665
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Ariza, X.1
Bou, V.2
Vilarrasa, J.3
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5
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33748981866
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L. DeNapoli, A. Messere, D. Montesarchio, G. Piccialli and M. Varra, J. Chem. Soc., Perkin Trans. 1, 1997, 2079.
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(1997)
J. Chem. Soc., Perkin Trans. 1
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-
DeNapoli, L.1
Messere, A.2
Montesarchio, D.3
Piccialli, G.4
Varra, M.5
-
6
-
-
33645442965
-
-
note
-
Under these conditions the isomeric 6-0-sulfonylated product was not observed.
-
-
-
-
7
-
-
33645446414
-
-
note
-
1 and the dinitrophenyl hydrogens.
-
-
-
-
9
-
-
0032877854
-
-
B. Catalanotti, L. De Napoli, A. Galeone, L. Mayol, G. Oliviero, G. Piccialli and M. Varra, Eur. J. Org. Chem., 1999, 2235;
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(1999)
Eur. J. Org. Chem.
, pp. 2235
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Catalanotti, B.1
De Napoli, L.2
Galeone, A.3
Mayol, L.4
Oliviero, G.5
Piccialli, G.6
Varra, M.7
-
10
-
-
0028936034
-
-
L. De Napoli, A. Messere, D. Montesarchio and G. Piccialli, J. Org. Chem., 1995, 60, 2251;
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(1995)
J. Org. Chem.
, vol.60
, pp. 2251
-
-
De Napoli, L.1
Messere, A.2
Montesarchio, D.3
Piccialli, G.4
-
11
-
-
37049077192
-
-
L. De Napoli, A. Messere, D. Montesarchio, G. Piccialli, C. Santacroce and M. Varra, J. Chem. Soc., Perkin Trans, 1, 1994, 923.
-
(1994)
J. Chem. Soc., Perkin Trans, 1
, pp. 923
-
-
De Napoli, L.1
Messere, A.2
Montesarchio, D.3
Piccialli, G.4
Santacroce, C.5
Varra, M.6
-
12
-
-
84943870548
-
-
Compound 3a was compared to a sample prepared by acetylation of adenosine: H. Bredereck, Chem. Ber., 1947, 80, 401.
-
(1947)
Chem. Ber.
, vol.80
, pp. 401
-
-
Bredereck, H.1
-
13
-
-
33645435624
-
-
note
-
The main byproduct is the desulfonylated inosine 1a (50% yield).
-
-
-
-
16
-
-
33645447911
-
-
note
-
Direct formation of 1a might arise from direct desulfonylation.
-
-
-
-
17
-
-
33645448955
-
-
note
-
In the absence of H2O the cyclisation occurred in lower yields.
-
-
-
-
18
-
-
37049138901
-
-
Compound 4a was chromatographically and spectroscopically identical to a sample prepared by reaction of adenosine 3a with benzyl bromide according to: P. Brookes, A. Dipple and P. D. Lawley, J. Chem. Soc., 1968, 2026.
-
(1968)
J. Chem. Soc.
, pp. 2026
-
-
Brookes, P.1
Dipple, A.2
Lawley, P.D.3
-
20
-
-
33645432596
-
-
note
-
Only when the reaction mixture was heated for a long time, small amounts of 5a were formed.
-
-
-
-
21
-
-
33748738396
-
-
Compound 5a was compared with a sample prepared by addition of benzylamine to 6-chloro-9-(2′,3′,5′-tri-O-acetyl-D- ribofuranosyl)-9H-purine: A. P. Henderson, J. Riseborough, C. Bleasdale, W. Clegg, M. R. J. Elsegood and B. T. Golding, J. Chem. Soc., Perkin Trans, 1, 1997, 3407.
-
(1997)
J. Chem. Soc., Perkin Trans, 1
, pp. 3407
-
-
Henderson, A.P.1
Riseborough, J.2
Bleasdale, C.3
Clegg, W.4
Elsegood, M.R.J.5
Golding, B.T.6
-
22
-
-
33645446546
-
-
note
-
18O).
-
-
-
-
23
-
-
0030749164
-
-
See for example: C. R. Allerson, S. L. Chen and G. L. Verdine, J. Am. Chem. Soc., 1997, 119, 7423.
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(1997)
J. Am. Chem. Soc.
, vol.119
, pp. 7423
-
-
Allerson, C.R.1
Chen, S.L.2
Verdine, G.L.3
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