-
1
-
-
0020972939
-
-
For reviews on the chemistry, biochemistry, and synthesis of nucleoside analogs see:
-
For reviews on the chemistry, biochemistry, and synthesis of nucleoside analogs see:. Buchanan J.G. Prog. Chem. Org. Nat. Prod. 44 (1983) 243
-
(1983)
Prog. Chem. Org. Nat. Prod.
, vol.44
, pp. 243
-
-
Buchanan, J.G.1
-
4
-
-
33744907530
-
-
Reviews:. Padwa A. (Ed), Wiley, New York
-
Reviews:. In: Padwa A. (Ed). Dipolar Cycloaddition Chemistry (1984), Wiley, New York 1-176
-
(1984)
Dipolar Cycloaddition Chemistry
, pp. 1-176
-
-
-
5
-
-
0000629986
-
-
Trost B.M. (Ed), Pergamon Press, New York
-
Padwa A. In: Trost B.M. (Ed). Comprehensive Organic Synthesis Vol. 4 (1991), Pergamon Press, New York 1069-1109
-
(1991)
Comprehensive Organic Synthesis
, vol.4
, pp. 1069-1109
-
-
Padwa, A.1
-
6
-
-
0000250143
-
-
Katritzky A.R., Rees C.W., and Scriven E.F.V. (Eds), Pergamon Press, New York
-
Fan W.-Q., and Katritzky A.R. In: Katritzky A.R., Rees C.W., and Scriven E.F.V. (Eds). Comprehensive Heterocyclic Chemistry Vol. 4 (1996), Pergamon Press, New York 101
-
(1996)
Comprehensive Heterocyclic Chemistry
, vol.4
, pp. 101
-
-
Fan, W.-Q.1
Katritzky, A.R.2
-
7
-
-
2242439174
-
-
Padwa A., and Pearson W.H. (Eds), John Wiley, New York
-
Sha C.-K., and Mohanakrishnan A.K. In: Padwa A., and Pearson W.H. (Eds). Comprehensive Heterocyclic Compounds Vol. 59 (2002), John Wiley, New York 623
-
(2002)
Comprehensive Heterocyclic Compounds
, vol.59
, pp. 623
-
-
Sha, C.-K.1
Mohanakrishnan, A.K.2
-
8
-
-
0029030796
-
-
For classical application of the click-chemistry to the synthesis of nucleoside analogs see:
-
For classical application of the click-chemistry to the synthesis of nucleoside analogs see:. San-Felix A., Alvarez R., Velazquez S., De Clercq E., Balzarini J., and Camarasa M.J. Nucleosides and Nucleotides 14 3-5 (1995) 595
-
(1995)
Nucleosides and Nucleotides
, vol.14
, Issue.3-5
, pp. 595
-
-
San-Felix, A.1
Alvarez, R.2
Velazquez, S.3
De Clercq, E.4
Balzarini, J.5
Camarasa, M.J.6
-
10
-
-
0037099395
-
-
For Cu(I)-catalyzed azide-alkyne cycloadditions, see:
-
For Cu(I)-catalyzed azide-alkyne cycloadditions, see:. Rostotsev V.V., Green L.G., Fokin V.V., and Sharpless K.B. Angew. Chem. Int. Ed. 41 (2002) 2596
-
(2002)
Angew. Chem. Int. Ed.
, vol.41
, pp. 2596
-
-
Rostotsev, V.V.1
Green, L.G.2
Fokin, V.V.3
Sharpless, K.B.4
-
14
-
-
11844255741
-
-
Himo F., Lovell T., Hilgraf R., Rostovtsev V.V., Noodleman L., Sharpless K.B., and Fokin V.V. J. Am. Chem. Soc. 127 (2005) 210
-
(2005)
J. Am. Chem. Soc.
, vol.127
, pp. 210
-
-
Himo, F.1
Lovell, T.2
Hilgraf, R.3
Rostovtsev, V.V.4
Noodleman, L.5
Sharpless, K.B.6
Fokin, V.V.7
-
16
-
-
1642427382
-
-
For reviews on microwave-assisted reactions see:. Loupy A. (Ed), Wiley-VCH, Weinheim
-
For reviews on microwave-assisted reactions see:. De La Hoz A., Diaz-Ortis A., and Langa F. In: Loupy A. (Ed). Microwaves in Organic Synthesis (2002), Wiley-VCH, Weinheim 295-343
-
(2002)
Microwaves in Organic Synthesis
, pp. 295-343
-
-
De La Hoz, A.1
Diaz-Ortis, A.2
Langa, F.3
-
19
-
-
0141825080
-
-
Louerat F., Bougrin K., Loupy A., Retana A.M.O., Pagalday J., and Palacios F. Heterocycles 48 (1998) 161
-
(1998)
Heterocycles
, vol.48
, pp. 161
-
-
Louerat, F.1
Bougrin, K.2
Loupy, A.3
Retana, A.M.O.4
Pagalday, J.5
Palacios, F.6
-
21
-
-
0347717653
-
-
Savin K.A., Robertson M., Gerneret D., Green S., Hembre E.J., and Bishop J. Mol. Div. 7 (2003) 171
-
(2003)
Mol. Div.
, vol.7
, pp. 171
-
-
Savin, K.A.1
Robertson, M.2
Gerneret, D.3
Green, S.4
Hembre, E.J.5
Bishop, J.6
-
24
-
-
84981759555
-
-
α-Chlorosugar 1 was synthesized as described:
-
α-Chlorosugar 1 was synthesized as described:. Hoffer M. Chem. Ber. 93 (1960) 2777
-
(1960)
Chem. Ber.
, vol.93
, pp. 2777
-
-
Hoffer, M.1
-
25
-
-
0034602186
-
-
The spectral data of compound 2 are in accordance with the reported ones, see:
-
The spectral data of compound 2 are in accordance with the reported ones, see:. Stimac A., and Kobe J. Carbohydr. Res. 329 (2000) 317
-
(2000)
Carbohydr. Res.
, vol.329
, pp. 317
-
-
Stimac, A.1
Kobe, J.2
-
26
-
-
33744920118
-
-
note
-
The best combination was found to be azide/CuI/DIEA = 1/2/5.
-
-
-
-
27
-
-
33744910640
-
-
note
-
+.
-
-
-
-
29
-
-
33744933494
-
-
Note. General procedure for triazolyl-nucleosides synthesis under microwave irradiation (for general safety and cautions relating to the use of microwave apparatus see, for example, Refs. 5a,c)
-
-
-
-
30
-
-
33744925467
-
-
note
-
+.
-
-
-
|