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Volumn 68, Issue 1, 2012, Pages 214-225

Synthesis of 1,2,3-triazolo-nucleosides via the post-triazole N-alkylation

Author keywords

1,2,3 Triazoles; 2H 1,2,3 Triazole; Click chemistry; N Unsubstituted 1,2,3 triazole; Nucleosides

Indexed keywords

1,2,3 TRIAZOLO NUCLEOSIDE; TRIAZOLE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 82255175491     PISSN: 00404020     EISSN: 14645416     Source Type: Journal    
DOI: 10.1016/j.tet.2011.10.067     Document Type: Article
Times cited : (20)

References (99)
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  • 2
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    • For reviews on the synthesis and biological properties of 1,4-disubstituted-1H-1,2,3-triazolo-nucleosides, see: F. Amblard, J.H. Cho, and R.F. Schinazi Chem. Rev. 109 2009 4207
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    • For biological activity of derivatives 2 or 3, see: Refs. 9b-d or10 respectively: V.P. Kripovalov, and O.P. Shkurko Russ. Chem. Rev. 74 2005 339
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    • Kripovalov, V.P.1    Shkurko, O.P.2
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    • For preparation of structurally diverse 2-substituted-2H-1,2,3-triazoles with a functionalized alkyl, winyl, allyl or propargyl residue, see: Ref. 12: D.-K. Kim, J. Kim, and H.-J. Park Bioorg. Med. Chem. Lett. 14 2004 2401
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    • Kim, D.-K.1    Kim, J.2    Park, H.-J.3
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    • For the syntheses of NH-1,2,3-triazoles by the addition of hydrazoic acid, or sodium azide to alkynes, see: L.-H. Liu, J.-H. Wu, and C.-H. Yang J. Chin. Chem. Soc. 55 2008 414
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    • Liu, L.-H.1    Wu, J.-H.2    Yang, C.-H.3
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    • For the two-step syntheses of NH-1,2,3-triazoles by alkyne-organic azide cycloaddition, followed by deprotection of a preformed N-protected-1,2,3- triazole, see: Ref. 9g: Ref. 9g: J.C. Loren, A. Karasinski, V.V. Fokin, and K.B. Sharpless Synlett 2005 2847
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    • Loren, J.C.1    Karasinski, A.2    Fokin, V.V.3    Sharpless, K.B.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.