메뉴 건너뛰기




Volumn 47, Issue 28, 2006, Pages 4807-4811

A highly efficient microwave-assisted solvent-free synthesis of α- and β-2′-deoxy-1,2,3-triazolyl-nucleosides

Author keywords

1,3 Dipolar cycloaddition; Cu(I) SiO2; Microwave activation; Nucleoside analogs; Regiocontrolled process

Indexed keywords

ALPHA 2' DEOXY 1,2,3 TRIAZOLYL NUCLEOSIDE; AZIDO 2' DEOXYRIBOSE; BETA 2' DEOXY 1,2,3 TRIAZOLYL NUCLEOSIDE; CUPRIC ION; DEOXYRIBOSE; NUCLEOSIDE; UNCLASSIFIED DRUG;

EID: 33744901930     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2006.05.050     Document Type: Article
Times cited : (85)

References (31)
  • 1
    • 0020972939 scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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
  • 16
    • 1642427382 scopus 로고    scopus 로고
    • 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
  • 24
    • 84981759555 scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • note
    • The best combination was found to be azide/CuI/DIEA = 1/2/5.
  • 27
    • 33744910640 scopus 로고    scopus 로고
    • note
    • +.
  • 29
    • 33744933494 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • note
    • +.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.