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Volumn 9, Issue 15, 2011, Pages 5373-5388

Selection of the biological activity of DNJ neoglycoconjugates through click length variation of the side chain

Author keywords

[No Author keywords available]

Indexed keywords

ADAMANTANES; ALKYL CHAIN; CERAMIDES; CYSTIC FIBROSIS; DEOXYNOJIRIMYCIN; GAUCHER DISEASE; GLUCOSYLTRANSFERASES; GLYCOSIDASE INHIBITORS; ION-TRANSPORT; NEOGLYCOCONJUGATES; SIDE-CHAINS;

EID: 79960343811     PISSN: 14770520     EISSN: None     Source Type: Journal    
DOI: 10.1039/c1ob05119a     Document Type: Article
Times cited : (42)

References (77)
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    • (2008) Glycoscience: Chemistry and Chemical Biology
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    • p. 177231
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  • 47
    • 0032758909 scopus 로고    scopus 로고
    • Bromides were obtained by nucleophilic displacement of tosylates 6a-b and 9a-d using LiBr in acetone Modest yields have often been reported for the direct reductive alkylation of DNJ. For, an example, see:
    • Y. Xu S.-R. Choi M.-P. Kung H. F. Kung Nucl. Med. Biol. 1999 26 833 839
    • (1999) Nucl. Med. Biol. , vol.26 , pp. 833-839
    • Xu, Y.1    Choi, S.-R.2    Kung, M.-P.3    Kung, H.F.4
  • 55
    • 43749099014 scopus 로고    scopus 로고
    • This solvent system has been described to promote CuAAC between organo-soluble azides and alkynes with more efficiency than water/alcohol mixtures:
    • A. Baron Y. Blériot M. Sollogoub B. Vauzeilles Org. Biomol. Chem. 2008 6 1898 1901
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.