메뉴 건너뛰기




Volumn 16, Issue 6, 2008, Pages 2945-2954

Recognition of T·A interruption by 2′,4′-BNAs bearing heteroaromatic nucleobases through parallel motif triplex formation

Author keywords

Bridged nucleic acid (BNA); Locked nucleic acid (LNA); Oligonucleotide; Triplex

Indexed keywords

2 (N METHYLBENZAMIDO)THIAZOLE; 4 (3 BENZAMIDOPHENYL) 2 PYRIDONE; DOUBLE STRANDED DNA; NUCLEIC ACID BASE; OLIGONUCLEOTIDE; UNCLASSIFIED DRUG; BENZAMIDE DERIVATIVE; BRIDGED COMPOUND; NUCLEIC ACID;

EID: 40949119424     PISSN: 09680896     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bmc.2007.12.043     Document Type: Article
Times cited : (14)

References (42)
  • 11
    • 40949159043 scopus 로고    scopus 로고
    • note
    • The 2′,4′-BNA was independently synthesized by the group of Wengel et al. immediately after our first report (reference 8), and it is called a locked nucleic acid (LNA). See Ref. 12-14.
  • 17
    • 40949148373 scopus 로고    scopus 로고
    • note
    • The symbols and * indicate Watson-Crick and Hoogsteen hydrogen bonds, respectively.
  • 20
    • 40949157304 scopus 로고    scopus 로고
    • Angew. Chem. 2001, 113, 2149-2151.
    • Angew. Chem. 2001, 113, 2149-2151.
  • 32
    • 0035368411 scopus 로고    scopus 로고
    • Efficient recognition of the T·A interruption in an antiparallel motif triplex was also reported:
    • Efficient recognition of the T·A interruption in an antiparallel motif triplex was also reported:. Parel S.P., and Leumann C.J. Nucleic Acids Res. 29 (2001) 2260-2267
    • (2001) Nucleic Acids Res. , vol.29 , pp. 2260-2267
    • Parel, S.P.1    Leumann, C.J.2
  • 37
    • 40949153237 scopus 로고    scopus 로고
    • note
    • The structure of 3 was confirmed by X-ray crystallography. CCDC-183684. The X-ray crystallographic data can be obtained free of charge via www.ccdc.cam.ac.uk/conts/retrieving.html (or from the Cambridge Crystallographic Data Centre, 12 Union Road, Cambridge CB2 1EZ, UK; fax: +44 1223 336033; or deposit@ccdc.cam.ac.uk).
  • 38
    • 0031550888 scopus 로고    scopus 로고
    • Pd-catalyzed cross-coupling reaction of aryltosylates for the synthesis of nucleobase analogues was recently reported:
    • Pd-catalyzed cross-coupling reaction of aryltosylates for the synthesis of nucleobase analogues was recently reported:. Nagatsugi F., Uemura K., Nakashima S., Maeda M., and Sasaki S. Tetrahedron 53 (1997) 3035-3044
    • (1997) Tetrahedron , vol.53 , pp. 3035-3044
    • Nagatsugi, F.1    Uemura, K.2    Nakashima, S.3    Maeda, M.4    Sasaki, S.5
  • 42
    • 40949142527 scopus 로고    scopus 로고
    • note
    • The benzyl groups were replaced with silyl groups because it was difficult to remove the benzyl groups by hydrogenolysis after coupling with thiazole derivative. The harsh conditions required to remove the benzyl groups could have inactivated the Pd-catalyst.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.