An efficient approach to homochiral indane nucleosides

Tetrahedron Asymmetry

Volumn 20, Issue 16, 2009, Pages 1848-1853

  Ugliarolo, Esteban A ^a   Lantaño, Beatriz ^a   Moltrasio, Graciela Y ^a   Moglioni, Albertina G ^a  

^a UNIVERSIDAD DE BUENOS AIRES   (Argentina)

Author keywords

[No Author keywords available]

Indexed keywords

1 ( 5 AMINO 6 CHLOROPYRIMIDIN 4 YLAMINO)INDAN 2 OL; 1 (2 AMINO 6 CHLORO 9H PURIN 9 YL) 2,3 DIHYDRO 1H INDEN 2 OL; 1 (2 AMINO 6 CHLOROPYRIMIDIN 4 YLAMINO)INDAN 2 OL; 1 (2,5 DIAMINO 6 CHLORO PYRIMIDIN 4 YLAMINO)INDAN 2 OL; 1 (5 AMINO 7 CHLORO 3H [1,2,3]TRIAZOLO[4,5 D]PYRIMIDIN 3 YL) 2,3 DIHYDRO 1H INDEN 2 OL; 1 (6 CHLOROPURIN 9 YL)INDAN 2 OL; 1 [2 AMINO 6 CHLORO 5 (4 CHLOROPHENYLAZO)PYRIMIDIN 4 YLAMINO]INDAN 2 OL; 2 AMINO 9 [2 HYDROXY 2,3 DIHYDRO 1H INDEN 1 YL] 1H PURIN 6(9H)ONE; 3 [2 HYDROXYINDAN 1 YL] 3,6 DIHYDRO [1 2 3]TRIAZOLO[4,5 D]PYRIMIDIN 7 ONE; 3 [2 HYDROXYINDAN 1 YL] 3,6 DIHYDRO [1.2.3]TRIAZOLO[4,5 D]PYRIMIDIN 7 ONE; 5 AMINO 3 [2 HYDROXY 2,3 DIHYDRO 1H INDEN 1 YL] 3H [1,2,3]TRIAZOLO[4,5 D]PYRIMIDIN 7(6H)ONE; 5 AMINO 3 [2 HYDROXY 2,3 DIHYDRO 1H INDEN 1 YL](1,2,) 3H [1,2,3]TRIAZOLO[4,5 D]PYRIMIDIN 7(6H)ONE; 9 [2 HYDROXYINDAN 1 YL] 1,9 DIHYDROPURIN 6 ONE; BUTANOL; HYDROCHLORIC ACID; INDANONE DERIVATIVE; NUCLEOSIDE DERIVATIVE; SODIUM HYDROXIDE; SODIUM NITRATE; UNCLASSIFIED DRUG;

ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CHIRALITY; DIAZOTIZATION; ENANTIOMER; METHODOLOGY; POLYMERIZATION; PRIORITY JOURNAL; PROTON NUCLEAR MAGNETIC RESONANCE;

EID: 69749096131     PISSN: 09574166     EISSN: 1362511X     Source Type: Journal    
DOI: 10.1016/j.tetasy.2009.07.035     Document Type: Article

References (15)

1. De Clercq E. Rev. Med. Virol. 5 (1995) 149-165
2. Marquez V.E. Adv. Antiviral Drug Des. 2 (1996) 89-146
3. De Clercq E. J. Med. Chem. 38 (1995) 2491-2517
4. Cookson R., Dudfield P., Newton R., Ravenscroft P., Scopes D., and Cameron J. Eur. J. Med. Chem. Chim. Ther. 20 (1985) 375
5. Shearly Y.F., and Clayton J.D. J. Am. Chem. Soc. 88 (1966) 3885-3887
6. Kusaka T., Yamamoto H., Shibata M., Muroi M., Kishi T., and Mizuno K.T. J. Antibiot. 21 (1968) 255-261
7. Yaginuma S., Muto N., Tsujino M., Sudate Y., Hayashi M., and Otani M. J. Antibiot. 34 (1981) 359-366
8. Agrofolio L., Suhas E., Farese A., Condom R., Challand S.R., Earl R.A., and Gueldj R. Tetrahedron 50 (1994) 10611-10670
9. Klopman G., and Tu M. J. Med. Chem. 42 (1999) 992-998
10. Zong-Sheng L., Ren-Ping Q., Zhen-Jun Y., Liang-Ren Z., and Li-He Z. Tetrahedron: Asymmetry 17 (2006) 1056-1061
11. Finkielsztein L.M., Castro E.C., Fabian L.E., Moltrasio G.Y., Campos R.H., Cavallaro L.V., and Moglioni A.G. Eur. J. Med. Chem. 43 (2008) 1767-1773
12. Fernandez F., García-Mera X., Morales M., Vilariño L., Caamaño O., and De Clercq E. Tetrahedron 60 (2004) 9245-9253
13. Hergueta A.R., Fernandez F., Lopez C., Balzarini J., and De Clercq E. Chem. Pharm. Bull. 49 (2001) 1174-1177
14. Santana L., Teijeira M., Uriarte E., Balzarini J., and De Clercq E. Bioorg. Med. Chem. Lett. 8 (1998) 1349-1352
15. Borges J., Fernandez F., Garcia X., Hergueta A., Lopez C., Andrei G., Snoeck R., Witvrounw M., Balzarini J., and De Clercq E. Nucleosides Nucleotides 17 (1998) 1237-1253