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Volumn 73, Issue 12, 2008, Pages 4513-4525

Synthesis of galactofuranose-containing acceptor substrates for mycobacterial galactofuranosyltransferases

Author keywords

[No Author keywords available]

Indexed keywords

BIOCHEMICAL ENGINEERING; BIOCHEMISTRY; CARBOHYDRATES; CHEMICAL REACTIONS; DERIVATIVES; GLUCOSE; IODINE; MATHEMATICAL MODELS; MICROFLUIDICS; NUMERICAL METHODS; PLANNING; POLYSACCHARIDES; STRATEGIC PLANNING; SUGAR (SUCROSE); SUGARS; SYNTHESIS (CHEMICAL); TARGETS; TELLURIUM COMPOUNDS;

EID: 45249089217     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo800457j     Document Type: Article
Times cited : (86)

References (69)
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    • (b) Lowary, T. L. In Glycoscience: Chemistry and Chemical Biology; Fraser-Reid, B., Tatsuta, K., Thiem, J., Eds.; Springer: Berlin, 2001; pp 2005-2080.
    • (2001) Glycoscience: Chemistry and Chemical Biology , pp. 2005-2080
    • Lowary, T.L.1
  • 10
    • 33745259764 scopus 로고    scopus 로고
    • Structure, Biosynthesis and Genetics of the Mycolic Acid-Arabinogalactan-Peptidoglycan Complex
    • Cole, S. T, Eisenach, K. D, McMurray, D. N, Jacobs, W. R, Jr, Eds, American Society for Microbiology: Washington, DC
    • (b) Mahapatra, S.; Basu, J.; Brennan, P. J.; Crick, D. C. Structure, Biosynthesis and Genetics of the Mycolic Acid-Arabinogalactan-Peptidoglycan Complex. In Tuberculosis and the Tubercle Bacillus; Cole, S. T., Eisenach, K. D., McMurray, D. N., Jacobs, W. R., Jr., Eds.; American Society for Microbiology: Washington, DC, 2005; pp 275-285.
    • (2005) Tuberculosis and the Tubercle Bacillus , pp. 275-285
    • Mahapatra, S.1    Basu, J.2    Brennan, P.J.3    Crick, D.C.4
  • 16
    • 45249121842 scopus 로고    scopus 로고
    • The nomenclature for these enzymes, GlfT1 and GlfT2, was recently proposed (ref 7) and differs slightly from that used previously.
    • The nomenclature for these enzymes, GlfT1 and GlfT2, was recently proposed (ref 7) and differs slightly from that used previously.
  • 53
    • 45249118661 scopus 로고    scopus 로고
    • The increased amount of iodine, compared to that originally reported (ref 27) was to speed the completion of the reaction
    • The increased amount of iodine, compared to that originally reported (ref 27) was to speed the completion of the reaction.
  • 60
    • 33747078758 scopus 로고    scopus 로고
    • For some examples of one-pot approaches to oligosaccharides, see
    • (a) For some examples of one-pot approaches to oligosaccharides, see: Huang, L. J.; Wang, Z.; Li, X. N.; Ye, X. S.; Huang, X. F. Carbohydr. Res. 2006, 341, 1669-1679.
    • (2006) Carbohydr. Res , vol.341 , pp. 1669-1679
    • Huang, L.J.1    Wang, Z.2    Li, X.N.3    Ye, X.S.4    Huang, X.F.5
  • 66
    • 45249088363 scopus 로고    scopus 로고
    • The identity of the intermediates formed in these one-pot reactions was confirmed by TLC comparison with authentic standards of 50 and 54, which were obtained in the course of the synthesis of 5 and 6 Schemes 8 and 9
    • The identity of the intermediates formed in these one-pot reactions was confirmed by TLC comparison with authentic standards of 50 and 54, which were obtained in the course of the synthesis of 5 and 6 (Schemes 8 and 9).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.