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Volumn 54, Issue 8, 2013, Pages 850-853

1,2,3-Triazoles as leaving groups in purine chemistry: A three-step synthesis of N6-substituted-2-triazolyl-adenine nucleosides and photophysical properties thereof

Author keywords

Click chemistry; Fluorescence; Nucleophilic aromatic substitution; Nucleoside analogs; Triazolyl purine derivatives

Indexed keywords

1,2,3 TRIAZOLE DERIVATIVE; 2,6 BIS (1,2,3 TRIAZOL 1 YL)PURINE NUCLEOSIDE; N 6 2 (1,2,3 TRIAZOL 1 YL) ADENINE NUCLEOSIDE; NUCLEOSIDE ANALOG; UNCLASSIFIED DRUG;

EID: 84872311520     PISSN: 00404039     EISSN: 18733581     Source Type: Journal    
DOI: 10.1016/j.tetlet.2012.11.095     Document Type: Article
Times cited : (48)

References (34)
  • 3
    • 84857762597 scopus 로고    scopus 로고
    • CLL Trialists' collaborative group
    • CLL Trialists' collaborative group. Haematologica 2012, 97, 428-436.
    • (2012) Haematologica , vol.97
  • 34
    • 84862556953 scopus 로고    scopus 로고
    • Recent developments in glycosylation chemistry permit also the synthesis of 2′-deoxynucleosides with good β-selectivity
    • Recent developments in glycosylation chemistry permit also the synthesis of 2′-deoxynucleosides with good β-selectivity: F. Yang, Y. Zhu, and B. Yu Chem. Commun. 48 2012 7097 7099
    • (2012) Chem. Commun. , vol.48 , pp. 7097-7099
    • Yang, F.1    Zhu, Y.2    Yu, B.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.