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Volumn 74, Issue 6, 2009, Pages 2278-2289

2,3-Anhydrosugars in glycoside bond synthesis. Application to 2,6-dideoxypyranosides

Author keywords

[No Author keywords available]

Indexed keywords

ANHYDROSUGARS; GLYCOSIDE BONDS; HYDROXYL GROUPS; LEWIS ACIDS; NATURAL PRODUCTS; PYRANOSIDES; THIOGLYCOSIDES; TRI-N-BUTYLTIN;

EID: 64149102009     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo900131a     Document Type: Article
Times cited : (36)

References (57)
  • 19
    • 4143083511 scopus 로고    scopus 로고
    • Fraser-Reid, B, Tatsuta, K, Thiem, J, Eds, Springer-Verlag; Berlin
    • Lindhorst, T. K. In Glycoscience: Chemistry and Chemical Biology; Fraser-Reid, B., Tatsuta, K., Thiem, J., Eds.; Springer-Verlag; Berlin, 2001; pp 2393-2439.
    • (2001) Glycoscience: Chemistry and Chemical Biology , pp. 2393-2439
    • Lindhorst, T.K.1
  • 56
    • 64149120868 scopus 로고    scopus 로고
    • We also explored the possibility of producing a disaccharide containing two 2-thiotolyl groups by reaction of 30 with 8 (Table 1), thus providing a compound in which both C-S bonds could be reduced in a single step. Although the glycosylation reaction was successful, it was difficult to purify the product, and therefore, we adopted the approach outlined in Scheme 11, in which the thioaryl groups were removed in separate steps.
    • We also explored the possibility of producing a disaccharide containing two 2-thiotolyl groups by reaction of 30 with 8 (Table 1), thus providing a compound in which both C-S bonds could be reduced in a single step. Although the glycosylation reaction was successful, it was difficult to purify the product, and therefore, we adopted the approach outlined in Scheme 11, in which the thioaryl groups were removed in separate steps.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.